Patent Application
20160108380
The instant application contains a Sequence Listing which has been submitted electronically in ASCII format and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Nov. 23, 2015, is named 19240.1034US2_SL.txt and is 2,208,530 bytes in size.
Glioblastoma multiforme (GBM) is the most common form of brain cancer and among the most incurable and lethal of all human cancers. The current standard of care includes surgery, chemotherapy, and radiation therapy. However, the prognosis of GBM remains uniformly poor. There are few available targeted therapies and none that specifically target GBM.
The target population of GBM patients who may carry EGFR gene fusions and would benefit from targeted inhibition of EGFR kinase activity is estimated to correspond to 6,000 patients per year world-wide.
The invention is based, at least in part, on the discovery of a highly expressed class of gene fusions in GBM, which join the receptor tyrosine kinase (RTK) domain of EGFR genes to the coiled-coil domain of septin proteins, such as Septin-14, or fused to a polypeptide comprising a phosphoserine phosphatase (PSPH) protein or a polypeptide comprising a Cullin-associated and neddylation-dissociated (CAND) protein. The invention is based, at least in part, on the finding that EGFR-SEPT fusions, EGFR-PSPH fusions, and EGFR-CAND fusions identify a subset of GBM patients who will benefit from targeted inhibition of the tyrosine kinase activity of EGFR. Identification of fusions of EGFR genes in glioblastoma patients are useful therapeutic targets.
An aspect of the invention is directed to a purified fusion protein comprising a tyrosine kinase domain of an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein. In one embodiment, the purified fusion protein is essentially free of other human proteins.
An aspect of the invention is directed to a purified fusion protein comprising the tyrosine kinase domain of an EGFR protein fused 5′ to a polypeptide comprising the coiled-coil domain of a Septin protein. In one embodiment, the Septin protein is Septin-1, Septin-2, Septin-3, Septin-4, Septin-5, Septin-6, Septin-7, Septin-8, Septin-9, Septin-10, Septin-11, Septin-12, Septin-13, or Septin-14. In another embodiment, the Septin protein is Septin-14 (SEPT14). In another embodiment, the purified fusion protein is essentially free of other human proteins.
An aspect of the invention is directed to a purified fusion protein comprising the tyrosine kinase domain of an EGFR protein fused 5′ to a polypeptide comprising a phosphoserine phosphatase (PSPH) protein. In another embodiment, the purified fusion protein is essentially free of other human proteins.
An aspect of the invention is directed to a purified fusion protein comprising the tyrosine kinase domain of an EGFR protein fused 3′ to a polypeptide comprising a Cullin-associated and neddylation-dissociated (CAND) protein. In one embodiment, the CAND protein is CAND1, CAND2, or CAND3. In another embodiment, the purified fusion protein is essentially free of other human proteins.
An aspect of the invention is directed to a purified fusion protein encoded by an EGFR-SEPT14 nucleic acid, wherein EGFR-SEPT14 comprises a combination of exons 1-25 of EGFR located on human chromosome 7p11.2 spliced 5′ to a combination of exons 7-10 of SEPT14 located on human chromosome 7, wherein a genomic breakpoint occurs in any one of exons 1-25 of EGFR and any one of exons 7-10 of SEPT14. In another embodiment, the purified fusion protein is essentially free of other human proteins.
An aspect of the invention is directed to a purified fusion protein encoded by an EGFR-PSPH nucleic acid, wherein EGFR-PSPH comprises a combination of exons 1-25 of EGFR located on human chromosome 7p12 spliced 5′ to a combination of exons 1-10 of PSPH located on human chromosome 7p11.2, wherein a genomic breakpoint occurs in any one of exons 1-25 of EGFR and any one of exons 1-10 of PSPH. In another embodiment, the purified fusion protein is essentially free of other human proteins.
An aspect of the invention is directed to a purified fusion protein encoded by an EGFR-CAND1 nucleic acid, wherein EGFR-CAND1 comprises a combination of exons 1-25 of EGFR located on human chromosome 7p12 spliced 3′ to a combination of exons 1-16 of CAND1 located on human chromosome 12q14, wherein a genomic breakpoint occurs in any one of exons 1-25 of EGFR and any one of exons 1-16 of CAND1. In another embodiment, the purified fusion protein is essentially free of other human proteins.
An aspect of the invention is directed to a synthetic nucleic acid encoding the EGFR fusion proteins described above.
An aspect of the invention is directed to a purified EGFR-SEPT14 fusion protein comprising SEQ ID NO: 1 or 5. In one embodiment, the purified fusion protein is essentially free of other human proteins.
An aspect of the invention is directed to a purified EGFR-SEPT14 fusion protein having a genomic breakpoint comprising SEQ ID NO: 4. In another embodiment, the purified fusion protein is essentially free of other human proteins.
An aspect of the invention is directed to a purified EGFR-PSPH fusion protein comprising SEQ ID NO: 7 or 11. In another embodiment, the purified fusion protein is essentially free of other human proteins.
An aspect of the invention is directed to a purified EGFR-PSPH fusion protein having a genomic breakpoint comprising SEQ ID NO: 10. In one embodiment, the purified fusion protein is essentially free of other human proteins.
An aspect of the invention is directed to a purified EGFR-CAND1 fusion protein comprising SEQ ID NO: 13 or 8495. In one embodiment, the purified fusion protein is essentially free of other human proteins.
An aspect of the invention is directed to a purified EGFR-CAND1 fusion protein having a genomic breakpoint comprising SEQ ID NO: 15. In one embodiment, the purified fusion protein is essentially free of other human proteins.
An aspect of the invention is directed to a synthetic nucleic acid encoding an EGFR-SEPT14 fusion protein comprising SEQ ID NO: 2.
An aspect of the invention is directed to a synthetic nucleic acid encoding an EGFR-SEPT14 fusion protein having a genomic breakpoint comprising SEQ ID NO: 4.
An aspect of the invention is directed to a synthetic nucleic acid encoding an EGFR-PSPH fusion protein comprising SEQ ID NO: 8.
An aspect of the invention is directed to a synthetic nucleic acid encoding an EGFR-PSPH fusion protein having a genomic breakpoint comprising SEQ ID NO: 10.
An aspect of the invention is directed to a synthetic nucleic acid encoding an EGFR-CAND1 fusion protein comprising SEQ ID NO: 14.
An aspect of the invention is directed to a synthetic nucleic acid encoding an EGFR-CAND1 fusion protein having a genomic breakpoint comprising SEQ ID NO: 15.
An aspect of the invention is directed to an antibody or antigen-binding fragment thereof that specifically binds to a purified fusion protein comprising a tyrosine kinase domain of an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein. In one embodiment, the fusion protein is an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND fusion protein. In another embodiment, the EGFR-SEPT fusion protein is EGFR-SEPT14. In one embodiment, the EGFR-SEPT fusion protein comprises the amino acid sequence of SEQ ID NO: 1, 3, or 5. In one embodiment, the EGFR-CAND fusion protein is EGFR-CAND1. In one embodiment, the EGFR-CAND fusion protein comprises the amino acid sequence of SEQ ID NO: 13, 16, or 8495.
An aspect of the invention is directed to an antibody or antigen-binding fragment thereof that specifically binds to a purified fusion protein comprising a tyrosine kinase domain of an EGFR protein fused to a polypeptide comprising the coiled-coil domain of a Septin protein. In another embodiment, the EGFR-SEPT fusion protein is EGFR-SEPT14. In one embodiment, the EGFR-SEPT fusion protein comprises the amino acid sequence of SEQ ID NO: 1, 3, or 5.
An aspect of the invention is directed to an antibody or antigen-binding fragment thereof that specifically binds to a purified fusion protein comprising a tyrosine kinase domain of an EGFR protein fused to a polypeptide comprising a phosphoserine phosphatase (PSPH) protein. In one embodiment, the EGFR-PSPH fusion protein comprises the amino acid sequence of SEQ ID NO: 7, 9, or 11.
An aspect of the invention is directed to an antibody or antigen-binding fragment thereof, that specifically binds to a purified fusion protein comprising a tyrosine kinase domain of an EGFR protein fused to a polypeptide comprising a Cullin-associated and neddylation-dissociated (CAND) protein. In one embodiment, the EGFR-CAND fusion protein is EGFR-CAND1. In one embodiment, the EGFR-CAND fusion protein comprises the amino acid sequence of SEQ ID NO: 13, 16, or 8495.
An aspect of the invention is directed to a composition for decreasing the expression level or activity of a fusion protein in a subject comprising the tyrosine kinase domain of an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein, the composition in an admixture of a pharmaceutically acceptable carrier comprising an inhibitor of the fusion protein. In one embodiment, the inhibitor comprises an antibody that specifically binds to an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion protein, or a fragment thereof; a small molecule that specifically binds to an EGFR protein; an antisense RNA or antisense DNA that decreases expression of an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion; a siRNA that specifically targets an EGFR-SEPT fusion gene, an EGFR-PSPH fusion gene, or an EGFR-CAND; or a combination thereof. In another embodiment, the CAND protein is CAND1. In a further embodiment, the SEPT protein is SEPT14. In some embodiments, the small molecule that specifically binds to an EGFR protein comprises AZD4547, NVP-BGJ398, PD173074, NF449, TK1258, BIBF-1120, BMS-582664, AZD-2171, TSU68, AB1010, AP24534, E-7080, LY2874455, or a combination thereof.
An aspect of the invention is directed to a method for treating a gene-fusion associated cancer in a subject in need thereof, the method comprising administering to the subject an effective amount of an EGFR fusion molecule inhibitor. In one embodiment, the gene-fusion associated cancer comprises glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. In one embodiment, the EGFR fusion comprises an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein. In one embodiment, the EGFR fusion protein is an EGFR-SEPT14 fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND1 fusion protein. In one embodiment, the inhibitor comprises an antibody that specifically binds to an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion protein, or a fragment thereof; a small molecule that specifically binds to an EGFR protein; an antisense RNA or antisense DNA that decreases expression of an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion; a siRNA that specifically targets an EGFR-SEPT fusion gene, an EGFR-PSPH fusion gene, or an EGFR-CAND; or a combination thereof. In one embodiment, the small molecule that specifically binds to an EGFR protein comprises AZD4547, NVP-BGJ398, PD173074, NF449, TK1258, BIBF-1120, BMS-582664, AZD-2171, TSU68, AB1010, AP24534, E-7080, LY2874455, or a combination thereof.
An aspect of the invention is directed to a method of decreasing growth of a solid tumor in a subject in need thereof, the method comprising administering to the subject an effective amount of an EGFR fusion molecule inhibitor, wherein the inhibitor decreases the size of the solid tumor. In one embodiment, the subject is afflicted with a gene-fusion associated cancer. In one embodiment, the gene-fusion associated cancer comprises glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. In one embodiment, the solid tumor comprises glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. In one embodiment, the EGFR fusion comprises an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein. In one embodiment, the EGFR fusion protein is an EGFR-SEPT14 fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND1 fusion protein. In one embodiment, the inhibitor comprises an antibody that specifically binds to an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion protein, or a fragment thereof; a small molecule that specifically binds to an EGFR protein; an antisense RNA or antisense DNA that decreases expression of an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion; a siRNA that specifically targets an EGFR-SEPT fusion gene, an EGFR-PSPH fusion gene, or an EGFR-CAND; or a combination thereof. In one embodiment, the small molecule that specifically binds to an EGFR protein comprises AZD4547, NVP-BGJ398, PD173074, NF449, TK1258, BIBF-1120, BMS-582664, AZD-2171, TSU68, AB1010, AP24534, E-7080, LY2874455, or a combination thereof.
An aspect of the invention is directed to a method of reducing cell proliferation in a subject afflicted with a gene-fusion associated cancer, the method comprising administering to the subject an effective amount of an EGFR fusion molecule inhibitor, wherein the inhibitor decreases cell proliferation. In one embodiment, the gene-fusion associated cancer comprises glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. In one embodiment, the EGFR fusion comprises an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein. In one embodiment, the EGFR fusion protein is an EGFR-SEPT14 fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND1 fusion protein. In one embodiment, the inhibitor comprises an antibody that specifically binds to an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion protein, or a fragment thereof a small molecule that specifically binds to an EGFR protein; an antisense RNA or antisense DNA that decreases expression of an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion; a siRNA that specifically targets an EGFR-SEPT fusion gene, an EGFR-PSPH fusion gene, or an EGFR-CAND; or a combination thereof. In one embodiment, the small molecule that specifically binds to an EGFR protein comprises AZD4547, NVP-BGJ398, PD173074, NF449, TK1258, BIBF-1120, BMS-582664, AZD-2171, TSU68, AB1010, AP24534, E-7080, LY2874455, or a combination thereof.
An aspect of the invention is directed to a diagnostic kit for determining whether a sample from a subject exhibits a presence of an EGFR fusion, the kit comprising at least one oligonucleotide that specifically hybridizes to an EGFR fusion, or a portion thereof. In one embodiment, the oligonucleotides comprise a set of nucleic acid primers or in situ hybridization probes. In another embodiment, the oligonucleotide comprises SEQ ID NOS 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 87, 88, 89, or a combination thereof. In a further embodiment, the primers prime a polymerase reaction only when an EGFR fusion is present. In some embodiments, the fusion protein is an EGFR-SEPT14 fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND1 fusion protein. In other embodiments, the determining comprises gene sequencing, selective hybridization, selective amplification, gene expression analysis, or a combination thereof.
An aspect of the invention is directed to a diagnostic kit for determining whether a sample from a subject exhibits a presence of an EGFR fusion protein, the kit comprising an antibody that specifically binds to an EGFR fusion protein comprising SEQ ID NO: 1, 3, 5, 7, 9, 11, 13, 16, or 8495, wherein the antibody will recognize the protein only when an EGFR fusion protein is present. In one embodiment, the fusion protein is an EGFR-SEPT14 fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND1 fusion protein. In one embodiment, the subject is afflicted with a gene-fusion associated cancer. In one embodiment, the gene-fusion associated cancer comprises glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma.
An aspect of the invention is directed to a method for detecting the presence of an EGFR fusion in a human subject. The method comprises obtaining a biological sample from the human subject; and detecting whether or not there is an EGFR fusion present in the subject. In one embodiment, the detecting comprises measuring EGFR fusion protein levels by ELISA using an antibody directed to SEQ ID NO: 1, 3, 5, 7, 9, 11, 13, 16, or 8495; western blot using an antibody directed to SEQ ID NO: 1, 3, 5, 7, 9, 11, 13, 16, or 8495; mass spectroscopy, isoelectric focusing, or a combination thereof.
An aspect of the invention is directed to a method for detecting the presence of an EGFR fusion in a human subject. The method comprises obtaining a biological sample from a human subject; and detecting whether or not there is a nucleic acid sequence encoding an EGFR fusion protein in the subject. In one embodiment, the nucleic acid sequence comprises any one of SEQ ID NOS: 2, 4, 8, 10, 14, and 15. In another embodiment, the detecting comprises using hybridization, amplification, or sequencing techniques to detect an EGFR fusion. In a further embodiment, the amplification uses primers comprising SEQ ID NOS 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 87, 88, or 89. In some embodiments, the fusion protein is an EGFR-SEPT14 fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND1 fusion protein.
To conform to the requirements for PCT patent applications, many of the figures presented herein are black and white representations of images originally created in color. In the below descriptions and the examples, the colored plots and images are described in terms of its appearance in black and white. The original color versions can be viewed in Frattini et al., (2013) Nature Genetics, 45(10):1141-49 (including the accompanying Supplementary Information available in the on-line version of the manuscript available on the Nature Genetics web site). For the purposes of the PCT, the contents of Frattini et al., (2013) Nature Genetics, 45(10):1141-49, including the accompanying “Supplementary Information,” are herein incorporated by reference.
Gene fusions retaining the RTK-coding domain of EGFR are the most frequent gene fusion events in GBM. EGFR gene fusions occur in 7.6% of GBM patients and frequently implicate the Sept14 gene as the 3′ partner in the fusion, with a consistent breakpoint at the RNA level. This makes the EGFR fusions highly manageable genetic alterations both diagnostically and therapeutically. In one embodiment, EGFR fusions enhance the proliferative and migratory capacity of glioma cells. In another embodiment, the EGFR fusions also confer sensitivity to EGFR inhibition to human GBM grown as mouse xenografts. Gene fusions encompassing RTK-coding genes are thus implicated in the pathogenesis of GBM and provide a strong rationale for the inclusion of GBM patients harboring EGFR fusions in clinical trials based on EGFR inhibitors. The target population of GBM patients who may carry EGFR gene fusions can benefit from targeted inhibition of EGFR kinase activity, and is estimated to correspond to 20,000 patients per year world-wide (˜1,000 in USA/year).
Glioblastoma multiformes (GBMs) are the most common form of brain tumors in adults accounting for 12-15% of intracranial tumors and 50-60% of primary brain tumors. GBM is among the most lethal forms of human cancer. The history of successful targeted therapy of cancer largely coincides with the inactivation of recurrent and oncogenic gene fusions in hematological malignancies and recently in some types of epithelial cancer. GBM is among the most lethal and incurable forms of human cancer. Targeted therapies against common genetic alterations in GBM have not changed the dismal clinical outcome of the disease, most likely because they have systematically failed to eradicate the truly addicting oncoprotein activities of GBM. Recurrent chromosomal rearrangements resulting in the creation of oncogenic gene fusions have not been found in GBM.
GBM is among the most difficult forms of cancer to treat in humans (1). So far, the therapeutic approaches that have been tested against potentially important oncogenic targets in GBM have met limited success (2-4). Recurrent chromosomal translocations leading to production of oncogenic fusion proteins are viewed as initiating and addicting events in the pathogenesis of human cancer, thus providing the most desirable molecular targets for cancer therapy (5, 6). Recurrent and oncogenic gene fusions have not been found in GBM. Chromosomal rearrangements are hallmarks of hematological malignancies but recently they have also been uncovered in subsets of solid tumors (breast, prostate, lung and colorectal carcinoma) (7, 8). Important and successful targeted therapeutic interventions for patients whose tumors carry these rearrangements have stemmed from the discovery of functional gene fusions, especially when the translocations involve kinase-coding genes (BCR-ABL, EML4-ALK) (9, 10). GBM, the most common malignant brain tumor, remains one of the most challenging forms of cancer to treat. The abundance of passenger mutations and large regions of copy number alterations has complicated the definition of the landscape of driver mutations in glioblastoma.
A hallmark of GBM is rampant chromosomal instability (CIN), which leads to aneuploidy (11). CIN and aneuploidy are early events in the pathogenesis of cancer (12). Without being bound by theory, genetic alterations targeting mitotic fidelity might be responsible for missegregation of chromosomes during mitosis, resulting in aneuploidy (13, 14).
Epidermal growth factor receptors (EGFR) are transmembrane glycoproteins and members of the protein kinase superfamily. This protein is a receptor for members of the epidermal growth factor family. EGFR is a cell surface protein that binds to epidermal growth factor. Binding of the protein to a ligand induces receptor dimerization and tyrosine autophosphorylation and leads to cell proliferation. Mutations that lead to EGFR overexpression or overactivity have been associated with a number of cancers, including lung cancer, anal cancers and glioblastoma multiforme.
Phosphoserine phosphatase (PSPH) is an enzyme responsible for the third and last step in L-serine formation. It catalyzes magnesium-dependent hydrolysis of L-phosphoserine and is also involved in an exchange reaction between L-serine and L-phosphoserine. Deficiency of this protein is thought to be linked to Williams syndrome.
The singular forms “a,” “an,” and “the” include plural reference unless the context clearly dictates otherwise.
The term “about” is used herein to mean approximately, in the region of, roughly, or around. When the term “about” is used in conjunction with a numerical range, it modifies that range by extending the boundaries above and below the numerical values set forth. In general, the term “about” is used herein to modify a numerical value above and below the stated value by a variance of 20%.
The practice of aspects of the present invention can employ, unless otherwise indicated, conventional techniques of cell biology, cell culture, molecular biology, transgenic biology, microbiology, recombinant DNA, and immunology, which are within the skill of the art. Such techniques are explained fully in the literature. See, e.g., Molecular Cloning A Laboratory Manual, 3rd Ed., ed. by Sambrook (2001), Fritsch and Maniatis (Cold Spring Harbor Laboratory Press: 1989); DNA Cloning, Volumes I and II (D. N. Glover ed., 1985); Oligonucleotide Synthesis (M. J. Gait ed., 1984); Mullis et al. U.S. Pat. No. 4,683,195; Nucleic Acid Hybridization (B. D. Hames & S. J. Higgins eds. 1984); Transcription and Translation (B. D. Hames & S. J. Higgins eds. 1984); Culture Of Animal Cells (R. I. Freshney, Alan R. Liss, Inc., 1987); Immobilized Cells and Enzymes (IRL Press, 1986); B. Perbal, A Practical Guide To Molecular Cloning (1984); the series, Methods In Enzymology (Academic Press, Inc., N.Y.), specifically, Methods In Enzymology, Vols. 154 and 155 (Wu et al. eds.); Gene Transfer Vectors For Mammalian Cells (J. H. Miller and M. P. Calos eds., 1987, Cold Spring Harbor Laboratory); Immunochemical Methods In Cell And Molecular Biology (Caner and Walker, eds., Academic Press, London, 1987); Handbook Of Experimental Immunology, Volumes I-IV (D. M. Weir and C. C. Blackwell, eds., 1986); Manipulating the Mouse Embryo, (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1986). All patents, patent applications and references cited herein are incorporated by reference in their entireties.
One skilled in the art can obtain a protein in several ways, which include, but are not limited to, isolating the protein via biochemical means or expressing a nucleotide sequence encoding the protein of interest by genetic engineering methods.
A protein is encoded by a nucleic acid (including, for example, genomic DNA, complementary DNA (cDNA), synthetic DNA, as well as any form of corresponding RNA). For example, it can be encoded by a recombinant nucleic acid of a gene. The proteins of the invention can be obtained from various sources and can be produced according to various techniques known in the art. For example, a nucleic acid that encodes a protein can be obtained by screening DNA libraries, or by amplification from a natural source. A protein can be a fragment or portion thereof. The nucleic acids encoding a protein can be produced via recombinant DNA technology and such recombinant nucleic acids can be prepared by conventional techniques, including chemical synthesis, genetic engineering, enzymatic techniques, or a combination thereof. For example, a fusion protein of the invention comprises a tyrosine kinase domain of an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein. For example, the fusion protein can be an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND fusion protein. An example of an EGFR-SEPT fusion protein is EGFR-SEPT14. In one embodiment, an EGFR-SEPT14 fusion polypeptide can have the amino acid sequence shown in SEQ ID NO: 1, 3, or 5. An example of an EGFR-PSPH fusion protein is a polypeptide having the amino acid sequence shown in SEQ ID NO: 7, 9, or 11. An example of an EGFR-CAND fusion protein is EGFR-CAND1. In one embodiment, an EGFR-CAND1 fusion polypeptide can have the amino acid sequence shown in SEQ ID NO: 13, 16, or 8495.
The Genbank ID for the EGFR gene is 1956. Four isoforms are listed for EGFR, e.g., having Genebank Accession Nos. NP_005219 (corresponding nucleotide sequence NM_005228); NP_958439 (corresponding nucleotide sequence NM_201282); NP_958440 (corresponding nucleotide sequence NM_201283); NP_958441 (corresponding nucleotide sequence NM_201284). The nucleotide and amino acid sequences can be readily obtained by one of ordinary skill in the art using the listed accession numbers.
The Genbank ID for the SEPT14 gene is 346288. The Genebank Accession No. for SEPT14 is NP_997249 (corresponding nucleotide sequence NM_207366). The nucleotide and amino acid sequences can be readily obtained by one of ordinary skill in the art using the listed accession numbers.
The Genbank ID for the PSPH gene is 5723. The Genebank Accession No. for PSPH is NP_004568 (corresponding nucleotide sequence NM_004577). The nucleotide and amino acid sequences can be readily obtained by one of ordinary skill in the art using the listed accession numbers.
The Genbank ID for the CAND1 gene is 55832. The Genebank Accession No. for CAND1 is NP_060918 (corresponding nucleotide sequence NM_018448). The nucleotide and amino acid sequences can be readily obtained by one of ordinary skill in the art using the listed accession numbers.
As used herein, an “EGFR fusion molecule” can be a nucleic acid which encodes a polypeptide corresponding to a fusion protein comprising a tyrosine kinase domain of an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein. For example, an EGFR fusion molecule can include an EGFR-SEPT fusion (e.g., an EGFR-SEPT14 fusion polypeptide comprising the amino acid sequence shown in SEQ ID NO: 1, 3, or 5, or comprising the nucleic acid sequence shown in SEQ ID NO: 2 or 4); an EGFR-PSPH fusion, (e.g., comprising the amino acid sequence shown in SEQ ID NO: 7, 9, or 11, or comprising the nucleic acid sequence shown in SEQ ID NO: 8 or 10), or an EGFR-CAND fusion (e.g., an EGFR-CAND1 fusion polypeptide comprising the amino acid sequence shown in SEQ ID NO: 13, 16, or 8495, or comprising the nucleic acid sequence shown in SEQ ID NO: 14 or 15). For example, an EGFR fusion molecule can include an EGFR-containing fusion comprising the amino acid sequence corresponding to Genebank Accession no. NP_005219, NP_958439, NP_958440, or NP_958441. AN EGFR fusion molecule can also include a tyrosine kinase domain of an EGFR protein fused to a protein encoded by any one of the genes listed in Table 10. AN EGFR fusion molecule can include a variant of the above described examples, such as a fragment thereof
The nucleic acid can be any type of nucleic acid, including genomic DNA, complementary DNA (cDNA), recombinant DNA, synthetic or semi-synthetic DNA, as well as any form of corresponding RNA. A cDNA is a form of DNA artificially synthesized from a messenger RNA template and is used to produce gene clones. A synthetic DNA is free of modifications that can be found in cellular nucleic acids and include, but are not limited to, histones and methylation. For example, a nucleic acid encoding anan EGFR EGFR fusion molecule can comprise a recombinant nucleic acid encoding such a protein. The nucleic acid can be a non-naturally occurring nucleic acid created artificially (such as by assembling, cutting, ligating or amplifying sequences). It can be double-stranded or single-stranded.
The invention further provides for nucleic acids that are complementary to an EGFR fusion molecule. Complementary nucleic acids can hybridize to the nucleic acid sequence described above under stringent hybridization conditions. Non-limiting examples of stringent hybridization conditions include temperatures above 30° C., above 35° C., in excess of 42° C., and/or salinity of less than about 500 mM, or less than 200 mM. Hybridization conditions can be adjusted by the skilled artisan via modifying the temperature, salinity and/or the concentration of other reagents such as SDS or SSC.
According to the invention, protein variants can include amino acid sequence modifications. For example, amino acid sequence modifications fall into one or more of three classes: substitutional, insertional or deletional variants. Insertions can include amino and/or carboxyl terminal fusions as well as intrasequence insertions of single or multiple amino acid residues. Insertions ordinarily will be smaller insertions than those of amino or carboxyl terminal fusions, for example, on the order of one to four residues. Deletions are characterized by the removal of one or more amino acid residues from the protein sequence. These variants ordinarily are prepared by site-specific mutagenesis of nucleotides in the DNA encoding the protein, thereby producing DNA encoding the variant, and thereafter expressing the DNA in recombinant cell culture.
In one embodiment, an EGFR fusion molecule comprises a protein or polypeptide encoded by a nucleic acid sequence encoding an EGFR fusion molecule, such as the sequences shown in SEQ ID NOS: 2, 4, 8, 10, 14, or 15. In some embodiments, the nuceleic acid sequence encoding an EGFR fusion molecule is about 70%, about 75%, about 80%, about 85%, about 90%, about 93%, about 95%, about 97%, about 98%, or about 99% identical to SEQ ID NOS: 2, 4, 8, 10, 14, or 15. In another embodiment, the polypeptide can be modified, such as by glycosylations and/or acetylations and/or chemical reaction or coupling, and can contain one or several non-natural or synthetic amino acids. An example of an EGFR fusion molecule is the polypeptide having the amino acid sequence shown in SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495. In some embodiments, the EGFR fusion molecule that is a polypeptide is about 70%, about 75%, about 80%, about 85%, about 90%, about 93%, about 95%, about 97%, about 98%, or about 99% identical to SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495. In another embodiment, an EGFR fusion molecule can be a fragment of an EGFR fusion protein. For example, the EGFR fusion molecule can encompass any portion of at least about 8 consecutive amino acids of SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495. The fragment can comprise at least about 10 amino acids, a least about 20 amino acids, at least about 30 amino acids, at least about 40 amino acids, at least about 50 amino acids, at least about 60 amino acids, or at least about 75 amino acids of SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495. Fragments include all possible amino acid lengths between about 8 and about 100 amino acids, for example, lengths between about 10 and about 100 amino acids, between about 15 and about 100 amino acids, between about 20 and about 100 amino acids, between about 35 and about 100 amino acids, between about 40 and about 100 amino acids, between about 50 and about 100 amino acids, between about 70 and about 100 amino acids, between about 75 and about 100 amino acids, or between about 80 and about 100 amino acids. Fragments include all possible amino acid lengths between about 100 and 800 amino acids, for example, lengths between about 125 and 800 amino acids, between about 150 and 800 amino acids, between about 175 and 800 amino acids, between about 200 and 800 amino acids, between about 225 and 800 amino acids, between about 250 and 800 amino acids, between about 275 and 800 amino acids, between about 300 and 800 amino acids, between about 325 and 800 amino acids, between about 350 and 800 amino acids, between about 375 and 800 amino acids, between about 400 and 800 amino acids, between about 425 and 800 amino acids, between about 450 and 800 amino acids, between about 475 and 800 amino acids, between about 500 and 800 amino acids, between about 525 and 800 amino acids, between about 550 and 800 amino acids, between about 575 and 800 amino acids, between about 600 and 800 amino acids, between about 625 and 800 amino acids, between about 650 and 800 amino acids, between about 675 and 800 amino acids, between about 700 and 800 amino acids, between about 725 and 800 amino acids, between about 750 and 800 amino acids, or between about 775 and 800 amino acids.
Chemical Synthesis.
Nucleic acid sequences encoding an EGFR fusion molecule can be synthesized, in whole or in part, using chemical methods known in the art. Alternatively, a polypeptide can be produced using chemical methods to synthesize its amino acid sequence, such as by direct peptide synthesis using solid-phase techniques. Protein synthesis can either be performed using manual techniques or by automation. Automated synthesis can be achieved, for example, using Applied Biosystems 431A Peptide Synthesizer (Perkin Elmer).
Optionally, polypeptides fragments can be separately synthesized and combined using chemical methods to produce a full-length molecule. For example, these methods can be utilized to synthesize a fusion protein of the invention. In one embodiment, a fusion protein of the invention comprises a tyrosine kinase domain of an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein. For example, the fusion protein can be an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND fusion protein. An example of an EGFR-SEPT fusion protein is EGFR-SEPT14. In one embodiment, an EGFR-SEPT14 fusion polypeptide can have the amino acid sequence shown in SEQ ID NO: 1, 3, or 5. An example of an EGFR-PSPH fusion protein is a polypeptide having the amino acid sequence shown in SEQ ID NO: 7, 9, or 11. An example of an EGFR-CAND fusion protein is EGFR-CAND1. In one embodiment, an EGFR-CAND1 fusion polypeptide can have the amino acid sequence shown in SEQ ID NO: 13, 16, or 8495.
Obtaining, Purifying and Detecting EGFR Fusion Molecules.
A polypeptide encoded by a nucleic acid, such as a nucleic acid encoding an EGFR fusion molecule, or a variant thereof, can be obtained by purification from human cells expressing a protein or polypeptide encoded by such a nucleic acid. Non-limiting purification methods include size exclusion chromatography, ammonium sulfate fractionation, ion exchange chromatography, affinity chromatography, and preparative gel electrophoresis.
A synthetic polypeptide can be substantially purified via high performance liquid chromatography (HPLC), such as ion exchange chromatography (IEX-HPLC). The composition of a synthetic polypeptide, such as an EGFR fusion molecule, can be confirmed by amino acid analysis or sequencing.
Other constructions can also be used to join a nucleic acid sequence encoding a polypeptide/protein of the claimed invention to a nucleotide sequence encoding a polypeptide domain which will facilitate purification of soluble proteins. Such purification facilitating domains include, but are not limited to, metal chelating peptides such as histidine-tryptophan modules that allow purification on immobilized metals, protein A domains that allow purification on immobilized immunoglobulin, and the domain utilized in the FLAGS extension/affinity purification system (Immunex Corp., Seattle, Wash.). Including cleavable linker sequences (i.e., those specific for Factor Xa or enterokinase (Invitrogen, San Diego, Calif.)) between the purification domain and a polypeptide encoded by a nucleic acid of the invention also can be used to facilitate purification. For example, the skilled artisan can use an expression vector encoding 6 histidine residues that precede a thioredoxin or an enterokinase cleavage site in conjunction with a nucleic acid of interest. The histidine residues facilitate purification by immobilized metal ion affinity chromatography, while the enterokinase cleavage site provides a means for purifying the polypeptide encoded by, for example, an EGFR-SEPT, EGFR-CAND, EGFR-PSPH, or EGFR-containing, nucleic acid.
Host cells which contain a nucleic acid encoding an EGFR fusion molecule, and which subsequently express the same, can be identified by various procedures known to those of skill in the art. These procedures include, but are not limited to, DNA-DNA or DNA-RNA hybridizations and protein bioassay or immunoassay techniques which include membrane, solution, or chip-based technologies for the detection and/or quantification of nucleic acid or protein. For example, the presence of a nucleic acid encoding an EGFR fusion molecule can be detected by DNA-DNA or DNA-RNA hybridization or amplification using probes or fragments of nucleic acids encoding the same. In one embodiment, a nucleic acid fragment of an EGFR fusion molecule can encompass any portion of at least about 8 consecutive nucleotides of SEQ ID NOS: 2, 8, or 14. In another embodiment, the fragment can comprise at least about 10 consecutive nucleotides, at least about 15 consecutive nucleotides, at least about 20 conseutive nucleotides, or at least about 30 consecutive nucleotides of SEQ ID NOS: 2, 8, or 14. Fragments can include all possible nucleotide lengths between about 8 and about 100 nucleotides, for example, lengths between about 15 and about 100 nucleotides, or between about 20 and about 100 nucleotides. Nucleic acid amplification-based assays involve the use of oligonucleotides selected from sequences encoding an EGFR fusion molecule nucleic acid, or EGFR fusion molecule nucleic acid to detect transformants which contain a nucleic acid encoding a protein or polypeptide of the same.
Protocols are known in the art for detecting and measuring the expression of a polypeptide encoded by a nucleic acid, such as a nucleic acid encoding an EGFR fusion molecule, using either polyclonal or monoclonal antibodies specific for the polypeptide. Non-limiting examples include enzyme-linked immunosorbent assay (ELISA), radioimmunoassay (RIA), and fluorescence activated cell sorting (FACS). A two-site, monoclonal-based immunoassay using monoclonal antibodies reactive to two non-interfering epitopes on a polypeptide encoded by a nucleic acid, such as a nucleic acid encoding an EGFR fusion molecule, can be used, or a competitive binding assay can be employed.
Labeling and conjugation techniques are known by those skilled in the art and can be used in various nucleic acid and amino acid assays. Methods for producing labeled hybridization or PCR probes for detecting sequences related to nucleic acid sequences encoding a protein, such as EGFR fusion molecule, include, but are not limited to, oligolabeling, nick translation, end-labeling, or PCR amplification using a labeled nucleotide. Alternatively, nucleic acid sequences, such as nucleic acids encoding an EGFR fusion molecule, can be cloned into a vector for the production of an mRNA probe. Such vectors are known in the art, are commercially available, and can be used to synthesize RNA probes in vitro by addition of labeled nucleotides and an appropriate RNA polymerase such as T7, T3, or SP6. These procedures can be conducted using a variety of commercially available kits (Amersham Pharmacia Biotech, Promega, and US Biochemical). Suitable reporter molecules or labels which can be used for ease of detection include radionuclides, enzymes, and fluorescent, chemiluminescent, or chromogenic agents, as well as substrates, cofactors, inhibitors, and/or magnetic particles.
A fragment can be a fragment of a protein, such as an EGFR fusion protein. For example, a fragment of an EGFR fusion can encompass any portion of at least about 8 consecutive amino acids of SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495. The fragment can comprise at least about 10 consecutive amino acids, at least about 20 consecutive amino acids, at least about 30 consecutive amino acids, at least about 40 consecutive amino acids, a least about 50 consecutive amino acids, at least about 60 consecutive amino acids, at least about 70 consecutive amino acids, at least about 75 consecutive amino acids, at least about 80 consecutive amino acids, at least about 85 consecutive amino acids, at least about 90 consecutive amino acids, at least about 95 consecutive amino acids, at least about 100 consecutive amino acids, at least about 200 consecutive amino acids, at least about 300 consecutive amino acids, at least about 400 consecutive amino acids, at least about 500 consecutive amino acids, at least about 600 consecutive amino acids, at least about 700 consecutive amino acids, or at least about 800 consecutive amino acids of SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495. Fragments include all possible amino acid lengths between about 8 and 100 about amino acids, for example, lengths between about 10 and about 100 amino acids, between about 15 and about 100 amino acids, between about 20 and about 100 amino acids, between about 35 and about 100 amino acids, between about 40 and about 100 amino acids, between about 50 and about 100 amino acids, between about 70 and about 100 amino acids, between about 75 and about 100 amino acids, or between about 80 and about 100 amino acids.
Host cells transformed with a nucleic acid sequence of interest can be cultured under conditions suitable for the expression and recovery of the protein from cell culture. The polypeptide produced by a transformed cell can be secreted or contained intracellularly depending on the sequence and/or the vector used. Expression vectors containing a nucleic acid sequence, such as a nucleic acid encoding an EGFR fusion molecule, can be designed to contain signal sequences which direct secretion of soluble polypeptide molecules encoded by the nucleic acid. Cell transfection and culturing methods are described in more detail below.
A eukaryotic expression vector can be used to transfect cells in order to produce proteins encoded by nucleotide sequences of the vector, e.g. those encoding an EGFR fusion molecule. Mammalian cells can contain an expression vector (for example, one that contains a nucleic acid encoding a fusion protein comprising a tyrosine kinase domain of an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein) via introducing the expression vector into an appropriate host cell via methods known in the art.
A host cell strain can be chosen for its ability to modulate the expression of the inserted sequences or to process the expressed polypeptide encoded by a nucleic acid, in the desired fashion. Such modifications of the polypeptide include, but are not limited to, acetylation, carboxylation, glycosylation, phosphorylation, lipidation, and acylation. Post-translational processing which cleaves a “prepro” form of the polypeptide also can be used to facilitate correct insertion, folding and/or function. Different host cells which have specific cellular machinery and characteristic mechanisms for post-translational activities (e.g., CHO, HeLa, MDCK, HEK293, and W138), are available from the American Type Culture Collection (ATCC; 10801 University Boulevard, Manassas, Va. 20110-2209) and can be chosen to ensure the correct modification and processing of the foreign protein.
An exogenous nucleic acid can be introduced into a cell via a variety of techniques known in the art, such as lipofection, microinjection, calcium phosphate or calcium chloride precipitation, DEAE-dextran-mediated transfection, or electroporation. Electroporation is carried out at approximate voltage and capacitance to result in entry of the DNA construct(s) into cells of interest (such as glioma cells (cell line SF188), neuroblastoma cells (cell lines IMR-32, SK-N-SH, SH-F and SH-N), astrocytes and the like). Other transfection methods also include modified calcium phosphate precipitation, polybrene precipitation, liposome fusion, and receptor-mediated gene delivery.
Cells that will be genetically engineered can be primary and secondary cells obtained from various tissues, and include cell types which can be maintained and propagated in culture. Non-limiting examples of primary and secondary cells include epithelial cells, neural cells, endothelial cells, glial cells, fibroblasts, muscle cells (such as myoblasts) keratinocytes, formed elements of the blood (e.g., lymphocytes, bone marrow cells), and precursors of these somatic cell types.
Vertebrate tissue can be obtained by methods known to one skilled in the art, such a punch biopsy or other surgical methods of obtaining a tissue source of the primary cell type of interest. In one embodiment, a punch biopsy or removal (e.g., by aspiration) can be used to obtain a source of cancer cells (for example, glioma cells, neuroblastoma cells, and the like). A mixture of primary cells can be obtained from the tissue, using methods readily practiced in the art, such as explanting or enzymatic digestion (for examples using enzymes such as pronase, trypsin, collagenase, elastase dispase, and chymotrypsin). Biopsy methods have also been described in U.S. Pat. No. 7,419,661 and PCT application publication WO 2001/32840, and each are hereby incorporated by reference.
Primary cells can be acquired from the individual to whom the genetically engineered primary or secondary cells are administered. However, primary cells can also be obtained from a donor, other than the recipient, of the same species. The cells can also be obtained from another species (for example, rabbit, cat, mouse, rat, sheep, goat, dog, horse, cow, bird, or pig). Primary cells can also include cells from an isolated or purified vertebrate tissue source grown attached to a tissue culture substrate (for example, flask or dish) or grown in a suspension; cells present in an explant derived from tissue; both of the aforementioned cell types plated for the first time; and cell culture suspensions derived from these plated cells. Secondary cells can be plated primary cells that are removed from the culture substrate and replated, or passaged, in addition to cells from the subsequent passages. Secondary cells can be passaged one or more times. These primary or secondary cells can contain expression vectors having a gene that encodes an EGFR fusion molecule.
Various culturing parameters can be used with respect to the host cell being cultured. Appropriate culture conditions for mammalian cells are well known in the art (Cleveland W L, et al., J Immunol Methods, 1983, 56(2): 221-234) or can be determined by the skilled artisan (see, for example, Animal Cell Culture: A Practical Approach 2nd Ed., Rickwood, D. and Hames, B. D., eds. (Oxford University Press: New York, 1992)). Cell culturing conditions can vary according to the type of host cell selected. Commercially available medium can be utilized. Non-limiting examples of medium include, for example, Minimal Essential Medium (MEM, Sigma, St. Louis, Mo.); Dulbecco's Modified Eagles Medium (DMEM, Sigma); Ham's F10 Medium (Sigma); HyClone cell culture medium (HyClone, Logan, Utah); RPMI-1640 Medium (Sigma); and chemically-defined (CD) media, which are formulated for various cell types, e.g., CD-CHO Medium (Invitrogen, Carlsbad, Calif.).
The cell culture media can be supplemented as necessary with supplementary components or ingredients, including optional components, in appropriate concentrations or amounts, as necessary or desired. Cell culture medium solutions provide at least one component from one or more of the following categories: (1) an energy source, usually in the form of a carbohydrate such as glucose; (2) all essential amino acids, and usually the basic set of twenty amino acids plus cysteine; (3) vitamins and/or other organic compounds required at low concentrations; (4) free fatty acids or lipids, for example linoleic acid; and (5) trace elements, where trace elements are defined as inorganic compounds or naturally occurring elements that can be required at very low concentrations, usually in the micromolar range.
The medium also can be supplemented electively with one or more components from any of the following categories: (1) salts, for example, magnesium, calcium, and phosphate; (2) hormones and other growth factors such as, serum, insulin, transferrin, and epidermal growth factor; (3) protein and tissue hydrolysates, for example peptone or peptone mixtures which can be obtained from purified gelatin, plant material, or animal byproducts; (4) nucleosides and bases such as, adenosine, thymidine, and hypoxanthine; (5) buffers, such as HEPES; (6) antibiotics, such as gentamycin or ampicillin; (7) cell protective agents, for example pluronic polyol; and (8) galactose. In one embodiment, soluble factors can be added to the culturing medium.
The mammalian cell culture that can be used with the present invention is prepared in a medium suitable for the type of cell being cultured. In one embodiment, the cell culture medium can be any one of those previously discussed (for example, MEM) that is supplemented with serum from a mammalian source (for example, fetal bovine serum (FBS)). In another embodiment, the medium can be a conditioned medium to sustain the growth of host cells.
Three-dimensional cultures can be formed from agar (such as Gey's Agar), hydrogels (such as matrigel, agarose, and the like; Lee et al., (2004) Biomaterials 25: 2461-2466) or polymers that are cross-linked. These polymers can comprise natural polymers and their derivatives, synthetic polymers and their derivatives, or a combination thereof. Natural polymers can be anionic polymers, cationic polymers, amphipathic polymers, or neutral polymers. Non-limiting examples of anionic polymers can include hyaluronic acid, alginic acid (alginate), carageenan, chondroitin sulfate, dextran sulfate, and pectin. Some examples of cationic polymers, include but are not limited to, chitosan or polylysine. (Peppas et al., (2006) Adv Mater. 18: 1345-60; Hoffman, A. S., (2002) Adv Drug Deliv Rev. 43: 3-12; Hoffman, A. S., (2001) Ann NY Acad Sci 944: 62-73). Examples of amphipathic polymers can include, but are not limited to collagen, gelatin, fibrin, and carboxymethyl chitin. Non-limiting examples of neutral polymers can include dextran, agarose, or pullulan. (Peppas et al., (2006) Adv Mater. 18: 1345-60; Hoffman, A. S., (2002) Adv Drug Deliv Rev. 43: 3-12; Hoffman, A. S., (2001) Ann NY Acad Sci 944: 62-73).
Cells to be cultured can harbor introduced expression vectors, such as plasmids. The expression vector constructs can be introduced via transformation, microinjection, transfection, lipofection, electroporation, or infection. The expression vectors can contain coding sequences, or portions thereof, encoding the proteins for expression and production. Expression vectors containing sequences encoding the produced proteins and polypeptides, as well as the appropriate transcriptional and translational control elements, can be generated using methods well known to and practiced by those skilled in the art. These methods include synthetic techniques, in vitro recombinant DNA techniques, and in vivo genetic recombination which are described in J. Sambrook et al., 2001, Molecular Cloning, A Laboratory Manual, Cold Spring Harbor Press, Plainview, N.Y. and in F. M. Ausubel et al., 1989, Current Protocols in Molecular Biology, John Wiley & Sons, New York, N.Y.
The invention provides methods for use of compounds that decrease the expression level or activity of an EFGR EGFR fusion molecule in a subject. In addition, the invention provides methods for using compounds for the treatment of a gene-fusion associated cancer. In one embodiment, the gene-fusion associated cancer comprises glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma.
As used herein, an “EGFR fusion molecule inhibitor” refers to a compound that interacts with an EGFR fusion molecule of the invention and modulates its activity and/or its expression. For example, the compound can decrease the activity or expression of an EGFR fusion molecule. The compound can be an antagonist of an EGFR fusion molecule (e.g., an EGFR fusion molecule inhibitor). Some non-limiting examples of EGFR fusion molecule inhibitors include peptides (such as peptide fragments comprising an EGFR fusion molecule, or antibodies or fragments thereof), small molecules, and nucleic acids (such as siRNA or antisense RNA specific for a nucleic acid comprising an EGFR fusion molecule). Antagonists of an EGFR fusion molecule decrease the amount or the duration of the activity of an EGFR fusion protein. In one embodiment, the fusion protein comprises a tyrosine kinase domain of an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein (e.g., EGFR-SEPT (such as EFGR-SEPT14), EGFR-PSPH, or EGFR-CAND (such as EGFR-CAND1)). Antagonists include proteins, nucleic acids, antibodies, small molecules, or any other molecule which decrease the activity of an EGFR fusion molecule.
The term “modulate,” as it appears herein, refers to a change in the activity or expression of an EGFR fusion molecule. For example, modulation can cause a decrease in protein activity, binding characteristics, or any other biological, functional, or immunological properties of an EGFR fusion molecule, such as an EGFR fusion protein.
In one embodiment, an EGFR fusion molecule inhibitor can be a peptide fragment of an EGFR fusion protein that binds to the protein itself.
For example, the EGFR fusion polypeptide can encompass any portion of at least about 8 consecutive amino acids of SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495. The fragment can comprise at least about 10 consecutive amino acids, at least about 20 consecutive amino acids, at least about 30 consecutive amino acids, at least about 40 consecutive amino acids, a least about 50 consecutive amino acids, at least about 60 consecutive amino acids, at least about 70 consecutive amino acids, at least about 75 consecutive amino acids, at least about 80 consecutive amino acids, at least about 85 consecutive amino acids, at least about 90 consecutive amino acids, at least about 95 consecutive amino acids, at least about 100 consecutive amino acids, at least about 200 consecutive amino acids, at least about 300 consecutive amino acids, at least about 400 consecutive amino acids, at least about 500 consecutive amino acids, at least about 600 consecutive amino acids, at least about 700 consecutive amino acids, or at least about 800 consecutive amino acids of SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495. Fragments include all possible amino acid lengths between about 8 and 100 about amino acids, for example, lengths between about 10 and about 100 amino acids, between about 15 and about 100 amino acids, between about 20 and about 100 amino acids, between about 35 and about 100 amino acids, between about 40 and about 100 amino acids, between about 50 and about 100 amino acids, between about 70 and about 100 amino acids, between about 75 and about 100 amino acids, or between about 80 and about 100 amino acids. These peptide fragments can be obtained commercially or synthesized via liquid phase or solid phase synthesis methods (Atherton et al., (1989) Solid Phase Peptide Synthesis: a Practical Approach. IRL Press, Oxford, England). The EGFR fusion peptide fragments can be isolated from a natural source, genetically engineered, or chemically prepared. These methods are well known in the art.
An EGFR fusion molecule inhibitor can be a protein, such as an antibody (monoclonal, polyclonal, humanized, chimeric, or fully human), or a binding fragment thereof, directed against an EGFR fusion molecule. An antibody fragment can be a form of an antibody other than the full-length form and includes portions or components that exist within full-length antibodies, in addition to antibody fragments that have been engineered. Antibody fragments can include, but are not limited to, single chain Fv (scFv), diabodies, Fv, and (Fab′)2, triabodies, Fc, Fab, CDR1, CDR2, CDR3, combinations of CDR's, variable regions, tetrabodies, bifunctional hybrid antibodies, framework regions, constant regions, and the like (see, Maynard et al., (2000) Ann. Rev. Biomed. Eng. 2:339-76; Hudson (1998) Curr. Opin. Biotechnol. 9:395-402). Antibodies can be obtained commercially, custom generated, or synthesized against an antigen of interest according to methods established in the art (see U.S. Pat. Nos. 6,914,128, 5,780,597, and 5,811,523; Roland E. Kontermann and Stefan Dübel (editors), Antibody Engineering, Vol. I & II, (2010) 2nd ed., Springer; Antony S. Dimitrov (editor), Therapeutic Antibodies: Methods and Protocols (Methods in Molecular Biology), (2009), Humana Press; Benny Lo (editor) Antibody Engineering: Methods and Protocols (Methods in Molecular Biology), (2004) Humana Press, each of which are hereby incorporated by reference in their entireties). For example, antibodies directed to an EGFR fusion molecule can be obtained commercially from Abcam, Santa Cruz Biotechnology, Abgent, R&D Systems, Novus Biologicals, etc. Human antibodies directed to an EGFR fusion molecule (such as monoclonal, humanized, fully human, or chimeric antibodies) can be useful antibody therapeutics for use in humans. In one embodiment, an antibody or binding fragment thereof is directed against SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495.
Inhibition of RNA encoding an EGFR fusion molecule can effectively modulate the expression of an EGFR fusion molecule Inhibitors are selected from the group comprising: siRNA; interfering RNA or RNAi; dsRNA; RNA Polymerase III transcribed DNAs; ribozymes; and antisense nucleic acids, which can be RNA, DNA, or an artificial nucleic acid.
Antisense oligonucleotides, including antisense DNA, RNA, and DNA/RNA molecules, act to directly block the translation of mRNA by binding to targeted mRNA and preventing protein translation. For example, antisense oligonucleotides of at least about 15 bases and complementary to unique regions of the DNA sequence encoding an EGFR fusion molecule can be synthesized, e.g., by conventional phosphodiester techniques (Dallas et al., (2006) Med. Sci. Monit. 12(4):RA67-74; Kalota et al., (2006) Handb. Exp. Pharmacol. 173:173-96; Lutzelburger et al., (2006) Handb. Exp. Pharmacol. 173:243-59). Antisense nucleotide sequences include, but are not limited to: morpholinos, 2′-O-methyl polynucleotides, DNA, RNA and the like.
siRNA comprises a double stranded structure containing from about 15 to about 50 base pairs, for example from about 21 to about 25 base pairs, and having a nucleotide sequence identical or nearly identical to an expressed target gene or RNA within the cell. The siRNA comprise a sense RNA strand and a complementary antisense RNA strand annealed together by standard Watson-Crick base-pairing interactions. The sense strand comprises a nucleic acid sequence which is substantially identical to a nucleic acid sequence contained within the target miRNA molecule. “Substantially identical” to a target sequence contained within the target mRNA refers to a nucleic acid sequence that differs from the target sequence by about 3% or less. The sense and antisense strands of the siRNA can comprise two complementary, single-stranded RNA molecules, or can comprise a single molecule in which two complementary portions are base-paired and are covalently linked by a single-stranded “hairpin” area. See also, McMnaus and Sharp (2002) Nat Rev Genetics, 3:737-47, and Sen and Blau (2006) FASEB J., 20:1293-99, the entire disclosures of which are herein incorporated by reference.
The siRNA can be altered RNA that differs from naturally-occurring RNA by the addition, deletion, substitution and/or alteration of one or more nucleotides. Such alterations can include addition of non-nucleotide material, such as to the end(s) of the siRNA or to one or more internal nucleotides of the siRNA, or modifications that make the siRNA resistant to nuclease digestion, or the substitution of one or more nucleotides in the siRNA with deoxyribo-nucleotides. One or both strands of the siRNA can also comprise a 3′ overhang. As used herein, a 3′ overhang refers to at least one unpaired nucleotide extending from the 3′-end of a duplexed RNA strand. For example, the siRNA can comprise at least one 3′ overhang of from 1 to about 6 nucleotides (which includes ribonucleotides or deoxyribonucleotides) in length, or from 1 to about 5 nucleotides in length, or from 1 to about 4 nucleotides in length, or from about 2 to about 4 nucleotides in length. For example, each strand of the siRNA can comprise 3′ overhangs of dithymidylic acid (“TT”) or diuridylic acid (“uu”).
siRNA can be produced chemically or biologically, or can be expressed from a recombinant plasmid or viral vector (for example, see U.S. Pat. No. 7,294,504 and U.S. Pat. No. 7,422,896, the entire disclosures of which are herein incorporated by reference). Exemplary methods for producing and testing dsRNA or siRNA molecules are described in U.S. Patent Application Publication No. 2002/0173478 to Gewirtz, U.S. Pat. No. 8,071,559 to Hannon et al., and in U.S. Pat. No. 7,148,342 to Tolentino et al., the entire disclosures of which are herein incorporated by reference.
In one embodiment, an siRNA directed to a human nucleic acid sequence comprising an EGFR fusion molecule can be generated against any one of SEQ ID NOS: 2, 4, 8, 10, 14, or 15. In another embodiment, an siRNA directed to a human nucleic acid sequence comprising a breakpoint of an EGFR fusion molecule can be generated against any one of SEQ ID NOS: 4, 10, or 15.
RNA polymerase III transcribed DNAs contain promoters, such as the U6 promoter. These DNAs can be transcribed to produce small hairpin RNAs in the cell that can function as siRNA or linear RNAs, which can function as antisense RNA. The EGFR fusion molecule inhibitor can comprise ribonucleotides, deoxyribonucleotides, synthetic nucleotides, or any suitable combination such that the target RNA and/or gene is inhibited. In addition, these forms of nucleic acid can be single, double, triple, or quadruple stranded. (See for example Bass (2001) Nature, 411:428-429; Elbashir et al., (2001) Nature, 411:494 498; U.S. Pat. No. 6,509,154; U.S. Patent Application Publication No. 2003/0027783; and PCT Publication Nos. WO 00/044895, WO 99/032619, WO 00/01846, WO 01/029058, WO 00/044914).
EGFR fusion molecule inhibitor can be a small molecule that binds to an EGFR fusion protein described herein and disrupts its function. Small molecules are a diverse group of synthetic and natural substances generally having low molecular weights. They can be isolated from natural sources (for example, plants, fungi, microbes and the like), are obtained commercially and/or available as libraries or collections, or synthesized. Candidate small molecules that inhibit an EGFR fusion protein can be identified via in silico screening or high-through-put (HTP) screening of combinatorial libraries according to methods established in the art (e.g., see Potyrailo et al., (2011) ACS Comb Sci. 13(6):579-633; Mensch et al., (2009) J Pharm Sci. 98(12):4429-68; Schnur (2008) Curr Opin Drug Discov Devel. 11(3):375-80; and Jhoti (2007) Ernst Schering Found Symp Proc. (3):169-85, each of which are hereby incorporated by reference in their entireties.) Most conventional pharmaceuticals, such as aspirin, penicillin, and many chemotherapeutics, are small molecules, can be obtained commercially, can be chemically synthesized, or can be obtained from random or combinatorial libraries as described below (see, e.g., Werner et al., (2006) Brief Funct. Genomic Proteomic 5(1):32-6).
Non-limiting examples of EGFR fusion molecule inhibitors include the EGFR inhibitors AZD4547 (see Gavine et al., (2012) Cancer Res, 72(8); 2045-56; see also PCT Application Publication No. WO2008/075068, each of which are hereby incorporated by reference in their entireties); NVP-BGJ398 (see Guagnano et al., (2011) J. Med. Chem., 54:7066-7083; see also U.S. Patent Application Publication No. 2008-0312248 A1, each of which are hereby incorporated by reference in their entireties); PD173074 (see Guagnano et al., (2011) J. Med. Chem., 54:7066-7083; see also Mohammadi et al., (1998) EMBO J., 17:5896-5904, each of which are hereby incorporated by reference in their entireties); NF449 (EMD Millipore (Billerica, Mass.) Cat. No. 480420; see also Krejci, (2010) the Journal of Biological Chemistry, 285(27):20644-20653, which is hereby incorporated by reference in its entirety); LY2874455 (Active Biochem; see Zhao et al. (2011) Mol Cancer Ther. (11):2200-10; see also PCT Application Publication No. WO 2010129509, each of which are hereby incorporated by reference in their entireties); TKI258 (Dovitinib); BIBF-1120 (Intedanib-Vargatef); BMS-582664 (Brivanib alaninate); AZD-2171 (Cediranib); TSU-68 (Orantinib); AB-1010 (Masitinib); AP-24534 (Ponatinib); and E-7080 (by Eisai). A non-limiting example of an EGFR fusion molecule inhibitor includes the inhibitor KHS101 (Wurdak et al., (2010) PNAS, 107(38): 16542-47, which is hereby incorporated by reference in its entirety).
Structures of EGFR fusion molecule inhibitors useful for the invention include, but are not limited to: the EGFR inhibitor AZD4547,
the EGFR inhibitor NVP-BGJ398,
the EGFR inhibitor PD173074,
the EGFR inhibitor LY2874455
and the EGFR inhibitor NF449 (EMD Millipore (Billerica, Mass.) Cat. No. 480420),
Other EGFR inhibitors include, but are not limited to:
A structure of an EGFR fusion molecule inhibitor useful for the invention includes, but is not limited to the inhibitor KHS101,
The invention provides a method of decreasing the growth of a solid tumor in a subject. The tumor is associated with, but not limited to glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. In one embodiment, the method comprises detecting the presence of an EGFR fusion molecule in a sample obtained from a subject. In some embodiments, the sample is incubated with an agent that binds to an EFGR fusion molecule, such as an antibody, a probe, a nucleic acid primer, and the like. In further embodiments, the method comprises administering to the subject an effective amount of an EGFR fusion molecule inhibitor, wherein the inhibitor decreases the size of the solid tumor.
The invention also provides a method for treating or preventing a gene-fusion associated cancer in a subject, such as, but not limited to, glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. In one embodiment, the method comprises detecting the presence of an EGFR fusion molecule in a sample obtained from a subject, the presence of the fusion being indicative of a gene-fusion associated cancer, and, administering to the subject in need a therapeutic treatment against a gene-fusion associated cancer. In some embodiments, the sample is incubated with an agent that binds to an EFGR fusion molecule, such as an antibody, a probe, a nucleic acid primer, and the like.
The invention also provides a method for decreasing in a subject in need thereof the expression level or activity of a fusion protein comprising the tyrosine kinase domain of an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein. In some embodiments, the method comprises obtaining a biological sample from the subject. In some embodiments, the sample is incubated with an agent that binds to an EGFR fusion molecule, such as an antibody, a probe, a nucleic acid primer, and the like. In some embodiments, the method comprises administering to the subject a therapeutic amount of a composition comprising an admixture of a pharmaceutically acceptable carrier an inhibitor of the fusion protein of the invention. In another embodiment, the method further comprises determining the fusion protein expression level or activity. In another embodiment, the method further comprises detecting whether the fusion protein expression level or activity is decreased as compared to the fusion protein expression level or activity prior to administration of the composition, thereby decreasing the expression level or activity of the fusion protein. In some embodiments, the fusion protein is an EGFR-PSPH fusion protein, an EGFR-CAND fusion protein, or an EGFR-SEPT fusion protein.
The administering step in each of the claimed methods can comprise a drug administration, such as EGFR fusion molecule inhibitor (for example, a pharmaceutical composition comprising an antibody that specifically binds to an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion protein, or a fragment thereof; a small molecule that specifically binds to an EGFR protein; an antisense RNA or antisense DNA that decreases expression of an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion; a siRNA that specifically targets an EGFR-SEPT fusion gene, an EGFR-PSPH fusion gene, or an EGFR-CAND). In one embodiment, the therapeutic molecule to be administered comprises a polypeptide of an EGFR fusion molecule, comprising at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 93%, at least about 95%, at least about 97%, at least about 98%, at least about 99%, or 100% of the amino acid sequence of SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495, and exhibits the function of decreasing expression of such a protein, thus treating a gene fusion-associated cancer. In another embodiment, administration of the therapeutic molecule decreases the size of the solid tumor associated with glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. In a further embodiment, administration of the therapeutic molecule decreases cell proliferation in a subject afflicted with a gene-fusion associated cancer.
In another embodiment, the therapeutic molecule to be administered comprises an siRNA directed to a human nucleic acid sequence comprising an EGFR fusion molecule. In one embodiment, the siRNA is directed to any one of SEQ ID NOS: 2, 4, 8, 10, 14, or 15. In a further embodiment, the therapeutic molecule to be administered comprises an antibody or binding fragment thereof, that is directed against SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495. In some embodiments, the therapeutic molecule to be administered comprises a small molecule that specifically binds to an EGFR protein, such as AZD4547, NVP-BGJ398, PD173074, NF449, TK1258, BIBF-1120, BMS-582664, AZD-2171, TSU68, AB1010, AP24534, E-7080, or LY2874455.
An EGFR fusion molecule, for example, a fusion between EGFR and SEPT, PSPH, or CAND, can be determined at the level of the DNA, RNA, or polypeptide. Optionally, detection can be determined by performing an oligonucleotide ligation assay, a confirmation based assay, a hybridization assay, a sequencing assay, an allele-specific amplification assay, a microsequencing assay, a melting curve analysis, a denaturing high performance liquid chromatography (DHPLC) assay (for example, see Jones et al, (2000) Hum Genet., 106(6):663-8), or a combination thereof. In one embodiment, the detection is performed by sequencing all or part of an EGFR fusion molecule (e.g., EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), EGFR-CAND fusion (such as an EGFR-CAND1 fusion), EGFR-PSPH), or by selective hybridization or amplification of all or part of an EGFR fusion molecule (e.g., EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), EGFR-CAND fusion (such as an EGFR-CAND1 fusion), EGFR-PSPH)). AN EGFR fusion molecule specific amplification (e.g., EGFR-SEPT (such as an EGFR-SEPT14), EGFR-CAND (such as an EGFR-CAND1), EGFR-PSPH nucleic acid specific amplification) can be carried out before the fusion identification step.
The invention provides for a method of detecting a chromosomal alteration in a subject afflicted with a gene-fusion associated cancer. In some emboidments, the gene-fusion associated cancer comprises glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. In one embodiment, the chromosomal alteration is an in-frame fused transcript described herein, for example an EGFR fusion molecule. An alteration in a chromosome region occupied by an EGFR fusion molecule such as a nucleic acid encoding an EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), an EGFR-CAND fusion (such as an EGFR-CAND1 fusion), or an EGFR-PSPH, can be any form of mutation(s), deletion(s), rearrangements) and/or insertions in the coding and/or non-coding region of the locus, alone or in various combination(s). Mutations can include point mutations. Insertions can encompass the addition of one or several residues in a coding or non-coding portion of the gene locus. Insertions can comprise an addition of between 1 and 50 base pairs in the gene locus. Deletions can encompass any region of one, two or more residues in a coding or non-coding portion of the gene locus, such as from two residues up to the entire gene or locus. Deletions can affect smaller regions, such as domains (introns) or repeated sequences or fragments of less than about 50 consecutive base pairs, although larger deletions can occur as well. Rearrangement includes inversion of sequences. The alteration in a chromosome region occupied by an EGFR fusion molecule, e.g., a nucleic acid encoding a an EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), an EGFR-CAND fusion (such as an EGFR-CAND1 fusion), or an EGFR-PSPH, can result in amino acid substitutions, RNA splicing or processing, product instability, the creation of stop codons, production of oncogenic fusion proteins, frame-shift mutations, and/or truncated polypeptide production. The alteration can result in the production of an EGFR fusion molecule, for example, a nucleic acid encoding an EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), an EGFR-CAND fusion (such as an EGFR-CAND1 fusion), or an EGFR-PSPH fusion, with altered function, stability, targeting or structure. The alteration can also cause a reduction, or even an increase in protein expression. In one embodiment, the alteration in the chromosome region occupied by an EGFR fusion molecule can comprise a chromosomal rearrangement resulting in the production of an EGFR fusion molecule, such as an EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), an EGFR-CAND fusion (such as an EGFR-CAND1 fusion), or an EGFR-PSPH fusion. This alteration can be determined at the level of the DNA, RNA, or polypeptide. In another embodiment, the detection or determination comprises nucleic acid sequencing, selective hybridization, selective amplification, gene expression analysis, or a combination thereof. In another embodiment, the detection or determination comprises protein expression analysis, for example by western blot analysis, ELISA, or other antibody detection methods.
The present invention provides a method for treating a gene-fusion associated cancer in a subject in need thereof. In one embodiment, the method comprises obtaining a sample from the subject to determine the level of expression of an EGFR fusion molecule in the subject. In some embodiments, the sample is incubated with an agent that binds to an EGFR fusion molecule, such as an antibody, a probe, a nucleic acid primer, and the like. In another embodiment, the detection or determination comprises nucleic acid sequencing, selective hybridization, selective amplification, gene expression analysis, or a combination thereof. In another embodiment, the detection or determination comprises protein expression analysis, for example by western blot analysis, ELISA, or other antibody detection methods. In some embodiments, the method further comprises assessing whether to administer an EGFR fusion molecule inhibitor based on the expression pattern of the subject. In further embodiments, the method comprises administering an EGFR fusion molecule inhibitor to the subject. In one embodiment, the gene-fusion associated cancer comprises glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma.
In one embodiment, the invention provides for a method of detecting the presence of altered RNA expression of an EFGR fusion molecule in a subject, for example, one afflicted with a gene-fusion associated cancer. In another embodiment, the invention provides for a method of detecting the presence of an EGFR fusion molecule in a subject. In some embodiments, the method comprises obtaining a sample from the subject to determine whether the subject expresses an EGFR fusion molecule. In some embodiments, the sample is incubated with an agent that binds to an EGFR fusion molecule, such as an antibody, a probe, a nucleic acid primer, and the like. In other embodiments, the detection or determination comprises nucleic acid sequencing, selective hybridization, selective amplification, gene expression analysis, or a combination thereof. In another embodiment, the detection or determination comprises protein expression analysis, for example by western blot analysis, ELISA, or other antibody detection methods. In some embodiments, the method further comprises assessing whether to administer an EGFR fusion molecule inhibitor based on the expression pattern of the subject. In further embodiments, the method comprises administering an EGFR fusion molecule inhibitor to the subject. Altered RNA expression includes the presence of an altered RNA sequence, the presence of an altered RNA splicing or processing, or the presence of an altered quantity of RNA. These can be detected by various techniques known in the art, including sequencing all or part of the RNA or by selective hybridization or selective amplification of all or part of the RNA.
In a further embodiment, the method can comprise detecting the presence or expression of an EGFR fusion molecule, such as a nucleic acid encoding an EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), an EGFR-CAND fusion (such as an EGFR-CAND1 fusion), or an EGFR-PSPH fusion. Altered polypeptide expression includes the presence of an altered polypeptide sequence, the presence of an altered quantity of polypeptide, or the presence of an altered tissue distribution. These can be detected by various techniques known in the art, including by sequencing and/or binding to specific ligands (such as antibodies). In one embodiment, the detecting comprises using a northern blot; real time PCR and primers directed to SEQ ID NOS: 2, 4, 8, 10, 14, or 15; a ribonuclease protection assay; a hybridization, amplification, or sequencing technique to detect an EGFR fusion molecule, such as one comprising SEQ ID NOS: 2, 4, 8, 10, 14, or 15; or a combination thereof. In another embodiment, the PCR primers comprise SEQ ID NOS 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 87, 88, or 89. In a further embodiment, primers used for the screening of EGFR fusion molecules, comprise SEQ ID NOS 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 87, 88, or 89. In some embodiments, primers used for genomic detection of an EGFR fusion comprise SEQ ID NOS 40, 41, 42, 43, 44, 45, or 89.
Various techniques known in the art can be used to detect or quantify altered gene or RNA expression or nucleic acid sequences, which include, but are not limited to, hybridization, sequencing, amplification, and/or binding to specific ligands (such as antibodies). Other suitable methods include allele-specific oligonucleotide (ASO), oligonucleotide ligation, allele-specific amplification, Southern blot (for DNAs), Northern blot (for RNAs), single-stranded conformation analysis (SSCA), PFGE, fluorescent in situ hybridization (FISH), gel migration, clamped denaturing gel electrophoresis, denaturing HLPC, melting curve analysis, heteroduplex analysis, RNase protection, chemical or enzymatic mismatch cleavage, ELISA, radio-immunoassays (RIA) and immuno-enzymatic assays (IEMA).
Some of these approaches (such as SSCA and constant gradient gel electrophoresis (CGGE)) are based on a change in electrophoretic mobility of the nucleic acids, as a result of the presence of an altered sequence. According to these techniques, the altered sequence is visualized by a shift in mobility on gels. The fragments can then be sequenced to confirm the alteration. Some other approaches are based on specific hybridization between nucleic acids from the subject and a probe specific for wild type or altered gene or RNA. The probe can be in suspension or immobilized on a substrate. The probe can be labeled to facilitate detection of hybrids. Some of these approaches are suited for assessing a polypeptide sequence or expression level, such as Northern blot, ELISA and RIA. These latter require the use of a ligand specific for the polypeptide, for example, the use of a specific antibody.
Hybridization.
Hybridization detection methods are based on the formation of specific hybrids between complementary nucleic acid sequences that serve to detect nucleic acid sequence alteration(s). A detection technique involves the use of a nucleic acid probe specific for a wild type or altered gene or RNA, followed by the detection of the presence of a hybrid. The probe can be in suspension or immobilized on a substrate or support (for example, as in nucleic acid array or chips technologies). The probe can be labeled to facilitate detection of hybrids. In one embodiment, the probe according to the invention can comprise a nucleic acid directed to SEQ ID NOS: 2, 4, 8, 10, 14, or 15. For example, a sample from the subject can be contacted with a nucleic acid probe specific for a gene encoding an EGFR fusion molecule, and the formation of a hybrid can be subsequently assessed. In one embodiment, the method comprises contacting simultaneously the sample with a set of probes that are specific for an EGFR fusion molecule. Also, various samples from various subjects can be investigated in parallel.
According to the invention, a probe can be a polynucleotide sequence which is complementary to and specifically hybridizes with a, or a target portion of a, gene or RNA corresponding to an EGFR fusion molecule. Useful probes are those that are complementary to the gene, RNA, or target portion thereof. Probes can comprise single-stranded nucleic acids of between 8 to 1000 nucleotides in length, for instance between 10 and 800, between 15 and 700, or between 20 and 500. Longer probes can be used as well. A useful probe of the invention is a single stranded nucleic acid molecule of between 8 to 500 nucleotides in length, which can specifically hybridize to a region of a gene or RNA that corresponds to an EGFR fusion molecule.
The sequence of the probes can be derived from the sequences of the EGFR fusion genes provided herein. Nucleotide substitutions can be performed, as well as chemical modifications of the probe. Such chemical modifications can be accomplished to increase the stability of hybrids (e.g., intercalating groups) or to label the probe. Some examples of labels include, without limitation, radioactivity, fluorescence, luminescence, and enzymatic labeling.
A guide to the hybridization of nucleic acids is found in e.g., Sambrook, ed., Molecular Cloning: A Laboratory Manual (3rd Ed.), Vols. 1-3, Cold Spring Harbor Laboratory, 1989; Current Protocols In Molecular Biology, Ausubel, ed. John Wiley & Sons, Inc., New York, 2001; Laboratory Techniques In Biochemistry And Molecular Biology: Hybridization With Nucleic Acid Probes, Part I. Theory and Nucleic Acid Preparation, Tijssen, ed. Elsevier, N.Y., 1993.
Sequencing.
Sequencing can be carried out using techniques well known in the art, using automatic sequencers. The sequencing can be performed on the complete EGFR fusion molecule or on specific domains thereof.
Amplification.
Amplification is based on the formation of specific hybrids between complementary nucleic acid sequences that serve to initiate nucleic acid reproduction. Amplification can be performed according to various techniques known in the art, such as by polymerase chain reaction (PCR), ligase chain reaction (LCR), strand displacement amplification (SDA) and nucleic acid sequence based amplification (NASBA). These techniques can be performed using commercially available reagents and protocols. Useful techniques in the art encompass real-time PCR, allele-specific PCR, or PCR based single-strand conformational polymorphism (SSCP). Amplification usually requires the use of specific nucleic acid primers, to initiate the reaction. For example, nucleic acid primers useful for amplifying sequences corresponding to an EGFR fusion molecule are able to specifically hybridize with a portion of the gene locus that flanks a target region of the locus. In one embodiment, amplification comprises using forward and reverse PCR primers directed to SEQ ID NOS: 2, 4, 8, 10, 14, or 15. Nucleic acid primers useful for amplifying sequences from an EGFR fusion molecule; the primers specifically hybridize with a portion of an EGFR fusion molecule. In certain subjects, the presence of an EGFR fusion molecule corresponds to a subject with a gene fusion-associated cancer. In one embodiment, amplification can comprise using forward and reverse PCR primers comprising nucleotide sequences of SEQ ID NOS 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 87, 88, or 89.
Non-limiting amplification methods include, e.g., polymerase chain reaction, PCR (PCR Protocols, A Guide To Methods And Applications, ed. Innis, Academic Press, N.Y., 1990 and PCR Strategies, 1995, ed. Innis, Academic Press, Inc., N.Y.); ligase chain reaction (LCR) (Wu (1989) Genomics 4:560; Landegren (1988) Science 241:1077; Barringer (1990) Gene 89:117); transcription amplification (Kwoh (1989) PNAS 86:1173); and, self-sustained sequence replication (Guatelli (1990) PNAS 87:1874); Q Beta replicase amplification (Smith (1997) J. Clin. Microbiol. 35:1477-1491), automated Q-beta replicase amplification assay (Burg (1996) Mol. Cell. Probes 10:257-271) and other RNA polymerase mediated techniques (e.g., NASBA, Cangene, Mississauga, Ontario; see also Berger (1987) Methods Enzymol. 152:307-316; U.S. Pat. Nos. 4,683,195 and 4,683,202; and Sooknanan (1995) Biotechnology 13:563-564). All the references stated above are incorporated by reference in their entireties.
The invention provides for a nucleic acid primer, wherein the primer can be complementary to and hybridize specifically to a portion of an EGFR fusion molecule, such as a nucleic acid (e.g., DNA or RNA), in certain subjects having a gene fusion-associated cancer. In one embodiment, the gene-fusion associated cancer comprises glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. Primers of the invention can be specific for fusion sequences in a nucleic acid (DNA or RNA) encoding an EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), an EGFR-CAND fusion (such as an EGFR-CAND1 fusion), or an EGFR-PSPH fusion. By using such primers, the detection of an amplification product indicates the presence of a fusion of a nucleic acid encoding an EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), an EGFR-CAND fusion (such as an EGFR-CAND1 fusion), or an EGFR-PSPH fusion. Examples of primers of this invention can be single-stranded nucleic acid molecules of about 5 to 60 nucleotides in length, or about 8 to about 25 nucleotides in length. The sequence can be derived directly from the sequence of an EGFR fusion molecule, e.g. a nucleic acid encoding an EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), an EGFR-CAND fusion (such as an EGFR-CAND1 fusion), or an EGFR-PSPH fusion. Perfect complementarity is useful to ensure high specificity; however, certain mismatch can be tolerated. For example, a nucleic acid primer or a pair of nucleic acid primers as described above can be used in a method for detecting the presence of a gene fusion-associated cancer in a subject. In one embodiment, primers can be used to detect an EGFR fusion molecule, such as a primer comprising SEQ ID NOS 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 87, 88, 89; or a combination thereof.
Specific Ligand Binding.
As discussed herein, a nucleic acid encoding an EGFR fusion molecule or expression of an EGFR fusion molecule, can also be detected by screening for alteration(s) in a sequence or expression level of a polypeptide encoded by the same. Different types of ligands can be used, such as specific antibodies. In one embodiment, the sample is contacted with an antibody specific for a polypeptide encoded by an EGFR fusion molecule and the formation of an immune complex is subsequently determined Various methods for detecting an immune complex can be used, such as ELISA, radioimmunoassays (RIA) and immuno-enzymatic assays (IEMA).
For example, an antibody can be a polyclonal antibody, a monoclonal antibody, as well as fragments or derivatives thereof having substantially the same antigen specificity. Fragments include Fab, Fab′2, or CDR regions. Derivatives include single-chain antibodies, humanized antibodies, or poly-functional antibodies. An antibody specific for a polypeptide encoded by an EGFR fusion molecule can be an antibody that selectively binds such a polypeptide. In one embodiment, the antibody is raised against a polypeptide encoded by an EGFR fusion molecule or an epitope-containing fragment thereof. Although non-specific binding towards other antigens can occur, binding to the target polypeptide occurs with a higher affinity and can be reliably discriminated from non-specific binding. In one embodiment, the method can comprise contacting a sample from the subject with an antibody specific for an EGFR fusion molecule, and determining the presence of an immune complex. Optionally, the sample can be contacted to a support coated with antibody specific for an EGFR fusion molecule. In one embodiment, the sample can be contacted simultaneously, or in parallel, or sequentially, with various antibodies specific for different forms of an EGFR fusion molecule, e.g., EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), an EGFR-CAND fusion (such as an EGFR-CAND1 fusion), or an EGFR-PSPH fusion.
The invention also provides for a diagnostic kit comprising products and reagents for detecting in a sample from a subject the presence of an EGFR fusion molecule. The kit can be useful for determining whether a sample from a subject exhibits reduced expression of an EGFR fusion molecule. For example, the diagnostic kit according to the present invention comprises any primer, any pair of primers, any nucleic acid probe and/or any ligand, or any antibody directed specifically to an EGFR fusion molecule. The diagnostic kit according to the present invention can further comprise reagents and/or protocols for performing a hybridization, amplification, or antigen-antibody immune reaction. In one embodiment, the kit can comprise nucleic acid primers that specifically hybridize to and can prime a polymerase reaction from an EGFR fusion molecule comprising SEQ ID NOS 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 87, 88, 89, or a combination thereof. In one embodiment, primers can be used to detect an EGFR fusion molecule, such as a primer comprising SEQ ID NOS 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 87, 88, 89; or a combination thereof. In a further embodiment, primers used for the screening of EGFR fusion molecules.
The diagnosis methods can be performed in vitro, ex vivo, or in vivo. These methods utilize a sample from the subject in order to assess the status of an EGFR fusion molecule. The sample can be any biological sample derived from a subject, which contains nucleic acids or polypeptides. Examples of such samples include, but are not limited to, fluids, tissues, cell samples, organs, and tissue biopsies. Non-limiting examples of samples include blood, liver, plasma, serum, saliva, urine, or seminal fluid. The sample can be collected according to conventional techniques and used directly for diagnosis or stored. The sample can be treated prior to performing the method, in order to render or improve availability of nucleic acids or polypeptides for testing. Treatments include, for instance, lysis (e.g., mechanical, physical, or chemical), centrifugation. The nucleic acids and/or polypeptides can be pre-purified or enriched by conventional techniques, and/or reduced in complexity. Nucleic acids and polypeptides can also be treated with enzymes or other chemical or physical treatments to produce fragments thereof. In one embodiment, the sample is contacted with reagents, such as probes, primers, or ligands, in order to assess the presence of an EGFR fusion molecule. Contacting can be performed in any suitable device, such as a plate, tube, well, or glass. In some embodiments, the contacting is performed on a substrate coated with the reagent, such as a nucleic acid array or a specific ligand array. The substrate can be a solid or semi-solid substrate such as any support comprising glass, plastic, nylon, paper, metal, or polymers. The substrate can be of various forms and sizes, such as a slide, a membrane, a bead, a column, or a gel. The contacting can be made under any condition suitable for a complex to be formed between the reagent and the nucleic acids or polypeptides of the sample.
Delivery of nucleic acids into viable cells can be effected ex vivo, in situ, or in vivo by use of vectors, such as viral vectors (e.g., lentivirus, adenovirus, adeno-associated virus, or a retrovirus), or ex vivo by use of physical DNA transfer methods (e.g., liposomes or chemical treatments). Non-limiting techniques suitable for the transfer of nucleic acid into mammalian cells in vitro include the use of liposomes, electroporation, microinjection, cell fusion, DEAE-dextran, and the calcium phosphate precipitation method (See, for example, Anderson, Nature, 1998) supplement to 392(6679):25( ). Introduction of a nucleic acid or a gene encoding a polypeptide of the invention can also be accomplished with extrachromosomal substrates (transient expression) or artificial chromosomes (stable expression). Cells can also be cultured ex vivo in the presence of therapeutic compositions of the present invention in order to proliferate or to produce a desired effect on or activity in such cells. Treated cells can then be introduced in vivo for therapeutic purposes.
Nucleic acids can be inserted into vectors and used as gene therapy vectors. A number of viruses have been used as gene transfer vectors, including papovaviruses, e.g., SV40 (Madzak et al., (1992) J Gen Virol. 73(Pt 6):1533-6), adenovirus (Berkner (1992) Curr Top Microbiol Immunol. 158:39-66; Berkner (1988) Biotechniques, 6(7):616-29; Gorziglia and Kapikian (1992) J Virol. 66(7):4407-12; Quantin et al., (1992) Proc Natl Acad Sci USA. 89(7):2581-4; Rosenfeld et al., (1992) Cell. 68(1):143-55; Wilkinson et al., (1992) Nucleic Acids Res. 20(9):2233-9; Stratford-Perricaudet et al., (1990) Hum Gene Ther. 1(3):241-56), vaccinia virus (Moss (1992) Curr Opin Biotechnol. 3(5):518-22), adeno-associated virus (Muzyczka, (1992) Curr Top Microbiol Immunol. 158:97-129; Ohi et al., (1990) Gene. 89(2):279-82), herpesviruses including HSV and EBV (Margolskee (1992) Curr Top Microbiol Immunol. 158:67-95; Johnson et al., (1992) Brain Res Mol Brain Res. 12(1-3):95-102; Fink et al., (1992) Hum Gene Ther. 3(1):11-9; Breakefield and Geller (1987) Mol Neurobiol. 1(4):339-71; Freese et al., (1990) Biochem Pharmacol. 40(10):2189-99), and retroviruses of avian (Bandyopadhyay and Temin (1984) Mol Cell Biol. 4(4):749-54; Petropoulos et al., (1992) J Virol. 66(6):3391-7), murine (Miller et al. (1992) Mol Cell Biol. 12(7):3262-72; Miller et al., (1985) J Virol. 55(3):521-6; Sorge et al., (1984) Mol Cell Biol. 4(9):1730-7; Mann and Baltimore (1985) J Virol. 54(2):401-7; Miller et al., (1988) J Virol. 62(11):4337-45), and human origin (Shimada et al., (1991) J Clin Invest. 88(3):1043-7; Helseth et al., (1990) J Virol. 64(12):6314-8; Page et al., (1990) J Virol. 64(11):5270-6; Buchschacher and Panganiban (1992) J Virol. 66(5):2731-9).
Non-limiting examples of in vivo gene transfer techniques include transfection with viral (e.g., retroviral) vectors (see U.S. Pat. No. 5,252,479, which is incorporated by reference in its entirety) and viral coat protein-liposome mediated transfection (Dzau et al., (1993) Trends in Biotechnology 11:205-210), incorporated entirely by reference). For example, naked DNA vaccines are generally known in the art; see Brower, (1998) Nature Biotechnology, 16:1304-1305, which is incorporated by reference in its entirety. Gene therapy vectors can be delivered to a subject by, for example, intravenous injection, local administration (see, e.g., U.S. Pat. No. 5,328,470) or by stereotactic injection (see, e.g., Chen, et al., (1994) Proc. Natl. Acad. Sci. USA 91:3054-3057). The pharmaceutical preparation of the gene therapy vector can include the gene therapy vector in an acceptable diluent, or can comprise a slow release matrix in which the gene delivery vehicle is imbedded. Alternatively, where the complete gene delivery vector can be produced intact from recombinant cells, e.g., retroviral vectors, the pharmaceutical preparation can include one or more cells that produce the gene delivery system.
For reviews of nucleic acid delivery protocols and methods see Anderson et al. (1992) Science 256:808-813; U.S. Pat. Nos. 5,252,479, 5,747,469, 6,017,524, 6,143,290, 6,410,010 6,511,847; and U.S. Application Publication No. 2002/0077313, which are all hereby incorporated by reference in their entireties. For additional reviews, see Friedmann (1989) Science, 244:1275-1281; Verma, Scientific American: 68-84 (1990); Miller (1992) Nature, 357: 455-460; Kikuchi et al. (2008) J Dermatol Sci. 50(2):87-98; Isaka et al. (2007) Expert Opin Drug Deliv. 4(5):561-71; Jager et al. (2007) Curr Gene Ther. 7(4):272-83; Waehler et al. (2007) Nat Rev Genet. 8(8):573-87; Jensen et al. (2007) Ann Med. 39(2):108-15; Herweijer et al. (2007) Gene Ther. 14(2):99-107; Eliyahu et al. (2005) Molecules 10(1):34-64; and Altaras et al. (2005) Adv Biochem Eng Biotechnol. 99:193-260, all of which are hereby incorporated by reference in their entireties.
An EGFR fusion nucleic acid can also be delivered in a controlled release system. For example, the EGFR fusion molecule can be administered using intravenous infusion, an implantable osmotic pump, a transdermal patch, liposomes, or other modes of administration. In one embodiment, a pump can be used (see Sefton (1987) Biomed. Eng. 14:201; Buchwald et al. (1980) Surgery 88:507; Saudek et al. (1989) N. Engl. J. Med. 321:574). In another embodiment, polymeric materials can be used (see Medical Applications of Controlled Release, Langer and Wise (eds.), CRC Pres., Boca Raton, Fla. (1974); Controlled Drug Bioavailability, Drug Product Design and Performance, Smolen and Ball (eds.), Wiley, New York (1984); Ranger and Peppas, (1983) J. Macromol. Sci. Rev. Macromol. Chem. 23:61; see also Levy et al. (1985) Science 228:190; During et al. (1989) Ann. Neurol. 25:351; Howard et al. (1989) J. Neurosurg. 71:105). In yet another embodiment, a controlled release system can be placed in proximity of the therapeutic target thus requiring only a fraction of the systemic dose (see, e.g., Goodson, in Medical Applications of Controlled Release, supra, vol. 2, pp. 115-138 (1984)). Other controlled release systems are discussed in the review by Langer (Science (1990) 249:1527-1533).
An inhibitor of the invention can be incorporated into pharmaceutical compositions suitable for administration, for example the inhibitor and a pharmaceutically acceptable carrier.
AN EGFR fusion molecule or inhibitor of the invention can be administered to the subject once (e.g., as a single injection or deposition). Alternatively, an EGFR fusion molecule or inhibitor can be administered once or twice daily to a subject in need thereof for a period of from about two to about twenty-eight days, or from about seven to about ten days. AN EGFR fusion molecule or inhibitor can also be administered once or twice daily to a subject for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 times per year, or a combination thereof. Furthermore, an EGFR fusion molecule or inhibitor of the invention can be co-administrated with another therapeutic. Where a dosage regimen comprises multiple administrations, the effective amount of the EGFR fusion molecule or inhibitor administered to the subject can comprise the total amount of gene product administered over the entire dosage regimen.
AN EGFR fusion molecule or inhibitor can be administered to a subject by any means suitable for delivering the EGFR fusion molecule or inhibitor to cells of the subject, such as cancer cells, e.g., glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. For example, an EGFR fusion molecule or inhibitor can be administered by methods suitable to transfect cells. Transfection methods for eukaryotic cells are well known in the art, and include direct injection of the nucleic acid into the nucleus or pronucleus of a cell; electroporation; liposome transfer or transfer mediated by lipophilic materials; receptor mediated nucleic acid delivery, bioballistic or particle acceleration; calcium phosphate precipitation, and transfection mediated by viral vectors.
The compositions of this invention can be formulated and administered to reduce the symptoms associated with a gene fusion-associated cancer, e.g., glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma, by any means that produces contact of the active ingredient with the agent's site of action in the body of a subject, such as a human or animal (e.g., a dog, cat, or horse). They can be administered by any conventional means available for use in conjunction with pharmaceuticals, either as individual therapeutic active ingredients or in a combination of therapeutic active ingredients. They can be administered alone, but are generally administered with a pharmaceutical carrier selected on the basis of the chosen route of administration and standard pharmaceutical practice.
A therapeutically effective dose of EGFR fusion molecule or inhibitor can depend upon a number of factors known to those or ordinary skill in the art. The dose(s) of the EGFR fusion molecule inhibitor can vary, for example, depending upon the identity, size, and condition of the subject or sample being treated, further depending upon the route by which the composition is to be administered, if applicable, and the effect which the practitioner desires the an EGFR fusion molecule inhibitor to have upon the nucleic acid or polypeptide of the invention. These amounts can be readily determined by a skilled artisan. Any of the therapeutic applications described herein can be applied to any subject in need of such therapy, including, for example, a mammal such as a dog, a cat, a cow, a horse, a rabbit, a monkey, a pig, a sheep, a goat, or a human.
Pharmaceutical compositions for use in accordance with the invention can be formulated in conventional manner using one or more physiologically acceptable carriers or excipients. The therapeutic compositions of the invention can be formulated for a variety of routes of administration, including systemic and topical or localized administration. Techniques and formulations generally can be found in Remmington's Pharmaceutical Sciences, Meade Publishing Co., Easton, Pa. (20th Ed., 2000), the entire disclosure of which is herein incorporated by reference. For systemic administration, an injection is useful, including intramuscular, intravenous, intraperitoneal, and subcutaneous. For injection, the therapeutic compositions of the invention can be formulated in liquid solutions, for example in physiologically compatible buffers such as Hank's solution or Ringer's solution. In addition, the therapeutic compositions can be formulated in solid form and redissolved or suspended immediately prior to use. Lyophilized forms are also included. Pharmaceutical compositions of the present invention are characterized as being at least sterile and pyrogen-free. These pharmaceutical formulations include formulations for human and veterinary use.
According to the invention, a pharmaceutically acceptable carrier can comprise any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like, compatible with pharmaceutical administration. The use of such media and agents for pharmaceutically active substances is well known in the art. Any conventional media or agent that is compatible with the active compound can be used. Supplementary active compounds can also be incorporated into the compositions.
A pharmaceutical composition containing EGFR fusion molecule inhibitor can be administered in conjunction with a pharmaceutically acceptable carrier, for any of the therapeutic effects discussed herein. Such pharmaceutical compositions can comprise, for example antibodies directed to an EGFR fusion molecule, or a variant thereof, or antagonists of an EGFR fusion molecule. The compositions can be administered alone or in combination with at least one other agent, such as a stabilizing compound, which can be administered in any sterile, biocompatible pharmaceutical carrier including, but not limited to, saline, buffered saline, dextrose, and water. The compositions can be administered to a patient alone, or in combination with other agents, drugs or hormones.
Sterile injectable solutions can be prepared by incorporating the EGFR fusion molecule inhibitor (e.g., a polypeptide or antibody) in the required amount in an appropriate solvent with one or a combination of ingredients enumerated herein, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the active compound into a sterile vehicle which contains a basic dispersion medium and the required other ingredients from those enumerated herein. In the case of sterile powders for the preparation of sterile injectable solutions, examples of useful preparation methods are vacuum drying and freeze-drying which yields a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.
In some embodiments, the EGFR fusion molecule inhibitor can be applied via transdermal delivery systems, which slowly releases the active compound for percutaneous absorption. Permeation enhancers can be used to facilitate transdermal penetration of the active factors in the conditioned media. Transdermal patches are described in for example, U.S. Pat. No. 5,407,713; U.S. Pat. No. 5,352,456; U.S. Pat. No. 5,332,213; U.S. Pat. No. 5,336,168; U.S. Pat. No. 5,290,561; U.S. Pat. No. 5,254,346; U.S. Pat. No. 5,164,189; U.S. Pat. No. 5,163,899; U.S. Pat. No. 5,088,977; U.S. Pat. No. 5,087,240; U.S. Pat. No. 5,008,110; and U.S. Pat. No. 4,921,475.
“Subcutaneous” administration can refer to administration just beneath the skin (i.e., beneath the dermis). Generally, the subcutaneous tissue is a layer of fat and connective tissue that houses larger blood vessels and nerves. The size of this layer varies throughout the body and from person to person. The interface between the subcutaneous and muscle layers can be encompassed by subcutaneous administration. This mode of administration can be feasible where the subcutaneous layer is sufficiently thin so that the factors present in the compositions can migrate or diffuse from the locus of administration. Thus, where intradermal administration is utilized, the bolus of composition administered is localized proximate to the subcutaneous layer.
Administration of the cell aggregates (such as DP or DS aggregates) is not restricted to a single route, but can encompass administration by multiple routes. For instance, exemplary administrations by multiple routes include, among others, a combination of intradermal and intramuscular administration, or intradermal and subcutaneous administration. Multiple administrations can be sequential or concurrent. Other modes of application by multiple routes will be apparent to the skilled artisan.
In other embodiments, this implantation method will be a one-time treatment for some subjects. In further embodiments of the invention, multiple cell therapy implantations will be required. In some embodiments, the cells used for implantation will generally be subject-specific genetically engineered cells. In another embodiment, cells obtained from a different species or another individual of the same species can be used. Thus, using such cells can require administering an immunosuppressant to prevent rejection of the implanted cells. Such methods have also been described in U.S. Pat. No. 7,419,661 and PCT application publication WO 2001/32840, and are hereby incorporated by reference.
A pharmaceutical composition of the invention is formulated to be compatible with its intended route of administration. Examples of routes of administration include parenteral, e.g., intravenous, intradermal, subcutaneous, oral (e.g., inhalation or ingestion), transdermal (topical), transmucosal, and rectal administration. Solutions or suspensions used for parenteral, intradermal, or subcutaneous application can include the following components: a sterile diluent such as water for injection, saline solution, fixed oils, polyethylene glycols, glycerine, propylene glycol or other synthetic solvents; antibacterial agents such as benzyl alcohol or methyl parabens; antioxidants such as ascorbic acid or sodium bisulfate; chelating agents such as ethylenediaminetetraacetic acid; buffers such as acetates, citrates or phosphates and agents for the adjustment of tonicity such as sodium chloride or dextrose. pH can be adjusted with acids or bases, such as hydrochloric acid or sodium hydroxide. The parenteral preparation can be enclosed in ampoules, disposable syringes or multiple dose vials made of glass or plastic.
Pharmaceutical compositions suitable for injectable use include sterile aqueous solutions (where water soluble) or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions. For intravenous administration, suitable carriers include physiological saline, bacteriostatic water, or phosphate buffered saline (PBS). In all cases, the composition must be sterile and should be fluid to the extent that easy syringability exists. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms such as bacteria and fungi. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, a pharmaceutically acceptable polyol like glycerol, propylene glycol, liquid polyetheylene glycol, and suitable mixtures thereof. The proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants. Prevention of the action of microorganisms can be achieved by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, ascorbic acid, thimerosal, and the like. In many cases, it can be useful to include isotonic agents, for example, sugars, polyalcohols such as mannitol, sorbitol, sodium chloride in the composition. Prolonged absorption of the injectable compositions can be brought about by including in the composition an agent which delays absorption, for example, aluminum monostearate and gelatin.
Sterile injectable solutions can be prepared by incorporating the inhibitor (e.g., a polypeptide or antibody or small molecule) of the invention in the required amount in an appropriate solvent with one or a combination of ingredients enumerated herein, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the active compound into a sterile vehicle which contains a basic dispersion medium and the required other ingredients from those enumerated herein. In the case of sterile powders for the preparation of sterile injectable solutions, examples of useful preparation methods are vacuum drying and freeze-drying which yields a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.
Oral compositions generally include an inert diluent or an edible carrier. They can be enclosed in gelatin capsules or compressed into tablets. For the purpose of oral therapeutic administration, the active compound can be incorporated with excipients and used in the form of tablets, troches, or capsules. Oral compositions can also be prepared using a fluid carrier and subsequently swallowed.
Pharmaceutically compatible binding agents, and/or adjuvant materials can be included as part of the composition. The tablets, pills, capsules, troches and the like can contain any of the following ingredients, or compounds of a similar nature: a binder such as microcrystalline cellulose, gum tragacanth or gelatin; an excipient such as starch or lactose, a disintegrating agent such as alginic acid, Primogel, or corn starch; a lubricant such as magnesium stearate or sterotes; a glidant such as colloidal silicon dioxide; a sweetening agent such as sucrose or saccharin; or a flavoring agent such as peppermint, methyl salicylate, or orange flavoring.
Systemic administration can also be by transmucosal or transdermal means. For transmucosal or transdermal administration, penetrants appropriate to the barrier to be permeated are used in the formulation. Such penetrants are generally known in the art, and include, for example, for transmucosal administration, detergents, bile salts, and fusidic acid derivatives. Transmucosal administration can be accomplished through the use of nasal sprays or suppositories. For transdermal administration, the active compounds are formulated into ointments, salves, gels, or creams as generally known in the art.
In some embodiments, the effective amount of the administered EGFR fusion molecule inhibitor is at least about 0.0001 μg/kg body weight, at least about 0.00025 μg/kg body weight, at least about 0.0005 μg/kg body weight, at least about 0.00075 μg/kg body weight, at least about 0.001 μg/kg body weight, at least about 0.0025 μg/kg body weight, at least about 0.005 μg/kg body weight, at least about 0.0075 μg/kg body weight, at least about 0.01 μg/kg body weight, at least about 0.025 μg/kg body weight, at least about 0.05 μg/kg body weight, at least about 0.075 μg/kg body weight, at least about 0.1 μg/kg body weight, at least about 0.25 μg/kg body weight, at least about 0.5 μg/kg body weight, at least about 0.75 μg/kg body weight, at least about 1 μg/kg body weight, at least about 5 μg/kg body weight, at least about 10 μg/kg body weight, at least about 25 μg/kg body weight, at least about 50 μg/kg body weight, at least about 75 μg/kg body weight, at least about 100 μg/kg body weight, at least about 150 μg/kg body weight, at least about 200 μg/kg body weight, at least about 250 μg/kg body weight, at least about 300 μg/kg body weight, at least about 350 μg/kg body weight, at least about 400 μg/kg body weight, at least about 450 μg/kg body weight, at least about 500 μg/kg body weight, at least about 550 μg/kg body weight, at least about 600 μg/kg body weight, at least about 650 μg/kg body weight, at least about 700 μg/kg body weight, at least about 750 μg/kg body weight, at least about 800 μg/kg body weight, at least about 850 μg/kg body weight, at least about 900 μg/kg body weight, at least about 950 μg/kg body weight, at least about 1000 μg/kg body weight, at least about 2000 μg/kg body weight, at least about 3000 μg/kg body weight, at least about 4000 μg/kg body weight, at least about 5000 μg/kg body weight, at least about 6000 μg/kg body weight, at least about 7000 μg/kg body weight, at least about 8000 μg/kg body weight, at least about 9500 μg/kg body weight, or at least about 10,000 μg/kg body weight.
Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Exemplary methods and materials are described below, although methods and materials similar or equivalent to those described herein can also be used in the practice or testing of the present invention.
All publications and other references mentioned herein are incorporated by reference in their entirety, as if each individual publication or reference were specifically and individually indicated to be incorporated by reference. Publications and references cited herein are not admitted to be prior art.
Examples are provided below to facilitate a more complete understanding of the invention. The following examples illustrate the exemplary modes of making and practicing the invention. However, the scope of the invention is not limited to specific embodiments disclosed in these Examples, which are for purposes of illustration only, since alternative methods can be utilized to obtain similar results.
To address the challenge of driver mutations in glioblastoma (GBM) and uncover new driver genes in human GBM, a computational platform was developed that integrates the analysis of copy number variations and somatic mutations from a whole-exome dataset. The full spectrum of in-frame gene fusions was unveiled from a large transcriptome dataset of glioblastoma. The analyses revealed focal copy number variations and mutations in all the genes previously implicated in glioblastoma pathogenesis. Recurrent copy number variations and somatic mutations were detected in 18 genes not yet implicated in glioblastoma. For each of the new genes, the occurrence of focal and recurrent copy number changes in addition to somatic mutations underscores the relevance for glioblastoma pathogenesis. Without being bound by theory, mutations in LZTR-1, a Keltch-BTB-BACK-BTB-BACK adaptor of Cul3-containing E3 ligase complexes impacted ubiquitination of LZTR-1 substrates. Loss-of-function mutations of CTNND2 (coding for δ-catenin) targeted a neural-specific gene and were associated with the transformation of glioma cells along the mesenchymal lineage, a hallmark of aggressive glioblastoma. Reconstitution of δ-catenin in mesenchymal glioma cells reprogrammed them towards a neuronal cell fate. Recurrent translocations were also identified that fuse in-frame the coding sequence of EGFR to several partners in 7.6% of tumors, with EGFR-Septin-14 scoring as the most frequent functional gene fusion in human glioblastoma. EGFR fusions enhance proliferation and motility of glioma cells and confer sensitivity to EGFR inhibition in glioblastoma xenografts. These results provide important insights into the pathogenesis of glioblastoma and highlight new targets for therapeutic intervention.
Glioblastoma (GBM) is the most common primary intrinsic malignant brain tumor affecting ˜10,000 new patients each year with a median survival rate of only 12-15 months1,2. Identifying and understanding the functional significance of the genetic alterations that drive initiation and progression of GBM is crucial to develop more effective therapies. Previous efforts in GBM genome characterization included array-based profiling of copy number changes, methylation and gene expression and targeted sequencing of candidate genes3-6. These studies identified somatic changes in well-known GBM genes (EGFR, PTEN, IDH1, TP53, NF1, etc.) and nominated putative cancer genes with somatic mutations, but the functional consequences of most alterations is unknown. The lack of strict correlation between somatic alterations and functionality in GBM is manifested by regions of large copy number variations (CNVs), in which the relevant gene(s) are masked within genomic domains encompassing many other genes. Furthermore, although the potential of next-generation sequencing of the whole coding exome is widely recognized for the nomination of new cancer genes, the elevated somatic mutation rate of GBM is a significant challenge for statistical approaches aimed to distinguish genes harboring driver from those with passenger mutations. A statistical approach was used to nominate driver genes in GBM from the integration of whole-exome sequencing data calling for somatic mutations with a CNVs analysis that prioritizes focality and magnitude of the genetic alterations.
Chromosomal rearrangements resulting in recurrent and oncogenic gene fusions are hallmarks of hematological malignancies and recently they have also been uncovered in solid tumors (breast, prostate, lung and colorectal carcinoma)7,8. Recently, a small subset of GBM harbor FGFR-TACC gene fusions were provided indicating that the patients with FGFR-TACC-positive tumors would benefit from targeted EGFR kinase inhibition9. It remains unknown whether gene fusions involving other RTK-coding genes exist in GBM to create different oncogene addicting states. A large RNA-sequencing dataset of primary GBM and glioma stem cells (GSCs) was analyzed and the global landscape of in-frame gene fusions in human GBM was reported.
Focal CNVs and point mutations provide exquisite information on candidate driver genes by pinpointing their exact location. Without being bound by theory, the integration of somatic point mutations and focal CNV information in a single framework will nominate candidate genes implicated in GBM. MutComFocal is an algorithm designed for this purpose, in which driver genes are ranked by an integrated recurrence, focality and mutation score (see Methods). Overall, this strategy was applied to a cohort of 139 GBM and matched normal DNA analyzed by whole exome sequencing to identify somatic mutations and 469 GBM were analyzed by the Affymetrix SNP6.0 platform to identify CNVs.
The whole-exome analysis identified a mean of 43 protein-changing somatic mutations per tumor sample. The distribution of substitutions shows a higher rate of transitions vs tranversions (67%), with a strong preference for C→T and G→A (55%) (
Among the commonly mutated and focally deleted genes that exhibited top MutComFocal scores and were validated in the independent GBM dataset, BCOR, LRP family members, HERC2, LZTR-1 and CTNND2. BCOR, a chromosome X-linked gene, encodes for a component of the nuclear co-repressor complex that is essential for normal development of the neuroectoderm and stem cell functions11-13. BCOR mutations have recently been described in retinoblastoma and medulloblastoma, thus indicating that loss-of-function mutations in BCOR are common genetic events in neuroectodermal tumors14,15. LRP1B is a member of the LDL receptor family and is among the most frequently mutated genes in human cancer (
Loss-of-Function Genetic Alterations Target the LZTR-1 and CTNND2 Genes in GBM
A gene that received one of the highest Del-Mut score by MutComFocal is LZTR-1 (
To address the potential function of LZTR-1 mutants, a homology model of LZTR-1 was built based in part on the crystal structures of the MATH-BTB-BACK protein SPOP26, the BTB-BACK-Kelch proteins KLHL3 and KLHL1127, and the Kelch domain of Keap128 (
Among the top ranking genes in MutComFocal, CTNND2 is the gene expressed at the highest levels in the normal brain. CTNND2 codes for -catenin, a member of the p120 subfamily of catenins that is expressed almost exclusively in the nervous system where it is crucial for neurite elongation, dendritic morphogenesis and synaptic plasticity31-33. Germ-line hemizygous loss of CTNND2 severely impairs cognitive function and underlies some forms of mental retardation34,35. CTNND2 shows a pronounced clustering of mutations in GBM. The observed spectrum of mutations includes four mutations located in the armadillo-coding domain and one in the region coding for the N-terminal coiled-coil domain (
It was asked whether the expression of CTNND2 is down-regulated during oncogenic transformation in the CNS Immunostaining experiments showed that δ-catenin is strongly expressed in the normal human and mouse brain with the highest expression in neurons (
Recurrent EGFR Fusions in GBM
To identify gene fusions in GBM, RNA-seq data was analyzed from a total of 185 GBM samples (161 primary GBM plus 24 short-term cultures of glioma stem-like cells (GSCs) freshly isolated from patients carrying primary GBM). The analysis of the RNA-seq dataset led to the discovery of 92 candidate rearrangements that give rise to in-frame fusion transcripts (Table 7). Beside the previously reported FGFR3-TACC3 fusions events, the most frequent recurrent in-frame fusions involved EGFR in 7.6% of samples (14/185, 3.8%-11.3% CI). Nine of the 14 EGFR fusions included the recurrent partners SEPT14 (6/185, 3.2%) and PSPH (3/185, 1.6%) as the 3′ gene segment in the fusion. Two in-frame highly expressed fusions were also found involving the neurotrophic tyrosine kinase receptor 1 gene (NTRK1) as 3′ gene with two different 5′ partners (NFASC-NTRK1 and BCAN-NTRK1). Fusions with a similar structure involving NTRK1 are commonly found in papillary thyroid carcinomas38. Using EXomeFuse, an algorithm for the reconstruction of genomic fusions from whole-exome data, EGFR-SEPT14 and NRTK1 fusions are the result of recurrent chromosomal translocations and reconstructed the corresponding genomic breakpoints (Table 8).
By sequencing the PCR products spanning the fusion breakpoint, each of the three types of recurrent in-frame fusion predictions (EGFR-SEPT14, EGFR-PSPH and NRTK1 fusions,
To confirm that GBM harbor recurrent EGFR fusions and determine the frequency in an independent dataset, cDNA was screened from a panel of 248 GBMs and discovered 10 additional cases harboring EGFR-SEPT14 fusions (4%). Conversely, NFASC-NTRK1 fusions were not detected in this dataset. The frequency of EGFR-PSPH fusions was 2.2% (3/135).
The discovery of recurrent EGFR fusions in GBM is of particular interest. EGFR is activated in a significant fraction of primary GBM (˜25%) by an in-frame deletion of exons 2-7 (EGFRvIII)39. To establish the functional relevance of EGFR fusions, it was determined whether the most frequent EGFR fusion in GBM (EGFR-SEPT14) provides an alternative mechanism of EGFR activation and confers sensitivity to EGFR inhibition. The EGFR-SEPT14 cDNA was cloned and prepared lentiviruses expressing EGFR-SEPT14, EGFRvIII or EGFR wild type. Transduction of the SNB19 glioma cell line (which lacks genomic alteration of EGFR) with the recombinant lentiviruses showed that cells expressing EGFR-SEPT14 or EGFRvIII proliferated at a rate that was 2-fold higher than control cells or cells expressing wild type EGFR (
Discussion
A computational pipeline is described for the nomination of somatic cancer genes. This approach computes frequency, magnitude and focality of CNVs at any loci in the human genome with the somatic mutation rate for the genes residing at that genomic location. Thus, two of the genetic hallmarks of driver cancer genes (focality of copy number aberrations and point mutations) are integrated into a single score. The approach identifies marks of positive somatic selection in large unbiased cancer genome studies by efficiently removing the large burden of passenger mutations that characterize most human tumors and will be applicable to the dissection of the genomic landscape of other cancer types.
Besides recognizing nearly all the known genes reported to have functional relevance in GBM, our study discovered and validated somatic mutations in 18 new genes, which also harbor focal and recurrent CNVs in a significant fraction of GBM. For some of these genes, their importance extends beyond GBM, as underscored by cross-tumor relevance (e.g. BCOR), and protein family recurrence (e.g. LRP family members). For example, mutations of LZTR-1 have been reported in other tumors. In particular, mutations of the highly conserved residues in the Keltch domain (W105, G248, T288) and in the second BTB-BACK domain (R810) reported here are recurrent events in other tumor types41. Thus, understanding the nature of the substrates of LZTR-1-Cul3 ubiquitin ligase activity will provide important insights into the pathogenesis of multiple cancer types.
The identification of genetic and epigenetic loss-of-function alterations of the CTNND2 gene clustered in mesenchymal GBM provides a clue to the genetic events driving this aggressive GBM subtype. The important functions of δ-catenin for such crucial neuronal morphogenesis activities as the coordinated control of axonal and dendritic arborization indicates that full-blown mesenchymal transformation in the brain requires loss of the master regulators constraining cell determination in the CNS along the default neuronal lineage. The ability of δ-catenin to reprogram glioma cells that express mesenchymal genes towards a neuronal fate unravels an unexpected plasticity of mesenchymal GBM that might be exploited therapeutically.
In this study, the landscape of gene fusions is reported from a large dataset of GBM analyzed by RNA-Sequencing. In-frame gene fusions retaining the RTK-coding domain of EGFR emerged as the most frequent gene fusion events in GBM. In this tumor, EGFR is frequently targeted by focal amplications and our finding underscores the strong recombinogenic probability of focally amplified genes, as recently reported for the myc locus in medulloblastoma42. Resembling intragenic rearrangements that generate the EGFRvIII allele, EGFR-SEPT14 fusions enhance the proliferative and migratory capacity of glioma cells. They also confer sensitivity to EGFR inhibition to human GBM grown as mouse xenografts. These findings highlight the relevance of gene fusions implicating RTK-coding genes in the pathogenesis of GBM9. They also provide a strong rationale for the inclusion of GBM patients harboring EGFR fusions in clinical trials based on EGFR inhibitors.
Methods
139 paired tumor-normal samples from TCGA were analyzed with the SAVI pipeline43. The SAVI algorithm estimates frequencies of variant alleles in sample as well as the difference in allele frequency between paired samples. The algorithm establishes posterior high credibility intervals for those frequencies and differences of frequencies, which can be used for genotyping the samples on the one hand, and detecting somatic mutations in the case of tumor/normal pairs of samples on the other. The algorithm allows for random sequencing errors and uses the Phred scores of the sequenced alleles as an estimate of their reliability. To integrate point mutation and 469 GBM CNV data (Affymetrix SNP6.0), MutComFocal (see below) was used. The MutComFocal algorithm assigns a driver score to each gene through three different strategies that give priority to lesions, samples, and genes in which there is less uncertainty regarding potential tumorigenic drivers. First, the focality component of the score is inversely proportional to the size of the genomic lesion to which a gene belongs and thus prioritizes more focal genomic lesions. Second, the recurrence component of the MutComFocal score is inversely proportional to the total number of genes altered in a sample, which prioritizes samples with a smaller number of altered genes. Finally, the mutation component of the score is inversely proportional to the total number of genes mutated in a sample, which achieves the two-fold goal of prioritizing mutated genes on one hand, and samples with a smaller number of mutations on the other.
161 RNA-Seq GBM tumor samples were also analyzed from TCGA plus 24 generated from our own dataset of GSCs. Nine of these samples previously reported in other studies were kept in the list to evaluate recurrence9. The samples were analyzed by means of the ChimeraScan algorithm in order to detect a list of gene fusion candidates44. Using the Pegasus annotation pipeline (http://sourceforge.net/projects/pegasus-fus/), the fusion transcript was reconstructed, the reading frame was annotated and protein domains were detected that are either conserved or lost in the new chimeric event. The genomic breakpoint of recurrent gene fusion RNA transcripts was also probed for using whole-exome sequencing data (EXome-Fuse algorithm)9. The Kaplan-Meier survival analysis for CTNND2 CNV and CTNND2 expression were obtained using the REMBRANDT glioma dataset.
SAVI (Statistical Algorithm for Variant Frequency Identification):
The frequency of alleles in a sample was estimated by the SAVI pipeline, which constructs an empirical Bayesian prior for those frequencies, using data from the whole sample, and obtains a posterior distribution and high credibility intervals for each alleleS1. The prior and posterior are distributed over a discrete set of frequencies with a precision of 1% and are connected by a modified binomial likelihood, which allows for some error rate. More precisely, a prior distribution p(f) of the frequency f and a prior for the error e uniform on the interval [0, E] was assumed for a fixed 0≦E≦1. The sequencing data at a particular allele is a random experiment producing a string of m (the total depth at the allele) bits with n “1” s (the variant depth at the allele). Assuming a binomial likelihood of the data and allowing for bits being misread due to random errors, the posterior probability P(f) of the frequency f is
where C is a normalization constant. For a particular allele, the value of E is determined by the quality of the nucleotides sequenced at that position as specified by their Phred scores. The SAVI pipeline takes as input the reads produced by the sequencing technology, filters out low quality reads and maps the rest onto a human reference genome. After mapping, a Bayesian prior for the distribution of allele frequencies for each sample is constructed by an iterative posterior update procedure, starting with a uniform prior. To genotype the sample, the posterior high credibility intervals were used for the frequency of the alleles at each genomic location. Alternatively, combining the Bayesian priors from different samples, posterior high credibility intervals were obtained for the difference between the samples of the frequencies of each allele. Finally, the statistically significant differences between the tumor and normal samples are reported as somatic variants. To estimate the positive prediction value of SAVI in the TCGA GBM samples, 41 mutations were selected for independent validation by Sanger sequencing. 39 of the 41 mutations were confirmed using Sanger sequencing, resulting in 0.95 (95% CI 0.83-0.99) validation rate.
Candidate genes were ranked by the number of somatic non-synonymous mutations. A robust fit of the ratio of non-synonymous to synonymous ratio was generated with a bisquare weighting function. Excess of non-synonymous alterations was estimated using a Poisson distribution with mean equal to the product of the ratio from the robust fit and the number of synonymous mutations. Genes in highly polymorphic genomic regions were filtered out based on an independent cohort of normal samples. The list of these regions includes families of genes known to generate false positives in somatic predictions (e.g. HLA, KRT and OR).
MutComFocal.
Key cancer genes are often found amplified or deleted in chromosomal regions containing many other genes. Point mutations and gene fusions, on the other hand, provide more specific information about which genes may be implicated in the oncogenic process. MutComFocal, a Bayesian approach aiming to identify driver genes by integrating CNV and point mutation data was developed.
For a particular sample, let (c1, N1), . . . , (ck, Nk) describe the amplification lesions in that sample so that Ni is the number of genes in the i-th lesion and ci is its copy number change from normal. For a gene belonging to the i-th lesion the amplification recurrence sample score is defined as ci/(Σjcj·Nj) and its amplification focality sample score is defined as (ci/Σj cj)·(1/Ni). To obtain the amplification recurrence and focality scores for a particular gene, the corresponding sample scores were summed over all samples and normalize the result so that each score sums to 1. The deletion and recurrence scores are defined in a similar manner. The mutation score is analogous to a recurrence score in which it was assumed that mutated genes belong to lesions with only one gene.
The amplification/mutation score is defined as the product of the two amplification scores and the mutation score while deletion/mutation score is defined as the product of the two deletion scores and the mutation score. The amplification/mutation and deletion/mutation scores are normalized to 1 and for each score, genes are divided into tiers iteratively, so that the top 2H remaining genes are included in the next tier, where H is the entropy of the scores of the remaining genes normalized to 1. Based on their tier across the different types of scores, genes are assigned to being either deleted/mutated or amplified/mutated and genes in the top tiers are grouped into contiguous regions. The top genes in each region are considered manually and selected for further functional validation.
The recurrence and focality scores can be interpreted as the posterior probabilities that a gene is driving the selection of the disease, under two different priors for this: one global and one local in nature. The recurrence score is higher if a gene participates in many samples that do not have too many altered genes, while the focality score is higher if the gene participates in many focal lesions. Besides lending strong support to the inference of a gene as a potential driver, the directionality of the copy number alteration (amplification or deletion) informs us of the likely behavior of the candidate gene as an oncogene or tumor suppressor, respectively.
The genes displayed in
RNA-Seq Bioinformatics Analysis.
161 RNA-Seq GBM tumor samples were analyzed from The Cancer Genome Atlas (TCGA), a public repository containing large-scale genome-sequencing of different cancers, plus 24 patients-derived GSCs. Nine of the GSCs samples reported in previous studies were kept in the list to evaluate recurrenceS2. The samples were analyzed by means of the ChimeraScanS3 algorithm in order to detect a list of gene fusion candidates. Briefly, ChimeraScan detects those reads that discordantly align to different transcripts of the same reference (split inserts). These reads provide an initial set of putative fusion candidates. Finally, the algorithm realigns the initially unmapped reads to the putative fusion candidates and detects those reads that align across the junction boundary (split reads). These reads provide the genomic coordinates of the breakpoint.
RNA-Seq analysis detected a total of 39,329 putative gene fusion events. In order to focus the experimental analysis on biologically relevant fused transcripts, Pegasus annotation pipeline (http://sourceforge.net/projects/pegasus-fus/) were applied. For each putative fusion, Pegasus reconstructs the entire fusion sequence on the base of genomic fusion breakpoint coordinates and gene annotations. Pegasus also annotates the reading frame of the resulting fusion sequences as either in-frame or frame-shift. Moreover, Pegasus detects the protein domains that are either conserved or lost in the new chimeric event by predicting the amino acid sequence and automatically querying the UniProt web service. On the basis of the Pegasus annotation report, relevant gene fusions were selected for further experimental validation according to the reading frame and the conserved/lost domains. The selected list (Table 7) was based on in-frame events expressed by ten or more reads and at least one read spanning the breaking point. To filter out candidate transplicing events, events with putative breakpoints at a distance of at least 25 kb were focused.
EXome-Fuse: Identification of Genetic Rearrangments Using Whole-Exome Data.
Although whole-exome sequencing data contains low intronic coverage that reduces the sensitivity for fusion discovery, it is readily available through the TCGA database. To characterize the genomic breakpoint of the chromosomal rearrangement, EXome-Fuse was designed: a gene fusion discovery pipeline particularly designed to analyze whole-exome data. For the samples harboring EGFR-SEPT14, EGFR-PSPH, NFASC-NTRK1, and BCAN-NTRK1 fusions in RNA, EXome-Fuse was applied to the corresponding whole-exome sequencing data deposited in TCGA. This algorithm can be divided into three stages: split insert identification, split read identification, and virtual reference alignment. Mapping against the human genome reference hg18 with BWA, all split inserts were first identified to compile a preliminary list of fusion candidates. This list was cut of any false positives produced from paralogous gene pairs using the Duplicated Genes Database and the EnsemblCompara GeneTrees4. Pseudogenes in the candidate list were annotated using the list from HUGO Gene Nomenclature Committee (HGNC) databaseS5 and given lower priority. Candidates were also filtered out between homologous genes, as well as those with homologous or low-complexity regions around the breakpoint. For the remaining fusion candidates, any supporting split reads and their mates were probed using BLAST with a word size of 16, identity cutoff of 90%, and an expectation cutoff of 10−4. Finally, a virtual reference was created for each fusion transcript and all reads were re-align to calculate a final tally of split inserts and split reads such that all aligning read pairs maintain F-R directionality.
Targeted Exon Sequencing
All protein-coding exons for the 24 genes of interest were sequenced using genomic DNA extracted from frozen tumors and matched blood. 500 ng of DNA from each sample were sheared to an average of 150 bp in a Covaris instrument for 360 seconds (Duty cycle—10%; intensity—5; cycles/Burst—200). Barcoded libraries were prepared using the Kapa High-Throughput Library Preparation Kit Standard (Kapa Biosystems). Libraries were amplified using the KAPA HiFi Library Amplification kit (Kapa Biosystems) (8 cycles). Libraries were quantified using Qubit Fluorimetric Quantitation (Invitrogen) and the quality and size assessed using an Agilent Bioanalyzer. An equimolar pool of the 4 barcoded libraries (300 ng each) was created and 1,200 ng was input to exon capture using one reaction tube of the custom Nimblegen SeqCap EZ (Roche) with custom probes target the coding exons of the 38 genes. Capture by hybridization was performed according to the manufacturer's protocols with the following modifications: 1 nmol of a pool of blocker oligonucleotides (complementary to the barcoded adapters), and (B) post-capture PCR amplification was done using the KAPA HiFi Library Amplification kit instead of the Phusion High-Fidelity PCR Master Mix with HF Buffer Kit, in a 60 μl volume, since the Kapa HiFi kit greatly reduced or eliminated the bias against GC-rich regions. The pooled capture library was quantified by Qubit (Invitrogen) and Bioanalyzer (Agilent) and sequenced in on an Illumina MiSeq sequencer using the 2×150 paired-end cycle protocol. Reads were aligned to the hg19 build of the human genome using BWA with duplicate removal using samtools as implemented by Illumina MiSeq Reporter. Variant detection was performed using GATK UnifiedGenotyper. Somatic mutations were identified for paired samples using SomaticSniper and filtered for frequency of less than 3% in normal and over 3% in tumor samples. Variants were annotated with Charity annotator to identify protein-coding changes and cross-referenced against known dbSNP, 1000 Genomes, and COSMIC mutations. Sanger sequencing was used to confirm each mutation from normal and tumor DNA.
Modeling of LZTR-1
Structural templates for the Kelch and BTB-BACK regions of human LZTR-1 were identified with HHpredS6. An initial 3D model was generated with the I-TASSER serverS7. The Cul3 N-terminal domain was docked onto the model by superposing the KLHL3BTB-BACK/Cul3NTD crystal structure (PDB ID 4HXI, Xi and Privé PLOS ONE 2013) onto the second LZTR-1 BTB-BACK domain. The model does not include higher quaternary structure, although many BTB domains, and many Kelch domains, are known to self-associateS8. The short linkage between the end of the first BACK domain and the beginning of the second BTB domain would appear to preclude an intrachain BTB-BTB pseudo-homodimer; without being bound by theory, LZTR-1 self-associates and forms higher order assemblies. Both BACK domains are the shorter, atypical form of the domain and consist of 2 helical hairpin motifs, as in SPOPS9,S10, and not the 4-hairpin motif seen most BTB-BACK-Kelch proteinsS10,S11. The model from the Kelch domain predicts an unusual 1+3 velcro arrangementS12, with the N-terminal region contributing strand d of blade 1 and the C-terminal region contributing strands a,b,c of the same blade, although an alternative 2+2 velcro model cannot be ruled out.
Cell Culture
SNB19 and U87 cells were cultured in DMEM supplemented with 10% Fetal Bovine Serum. Growth rate was determined by plating cells in six-well plates post 3 days after infection with the lentivirus indicated in Figure Legends. The number of viable cells was determined by trypan blue exclusion in triplicate cultures obtained from triplicate independent infections. Migration was evaluated by Confluent cells were scratched with a pipette tip and cultured in 0.25% FBS. After 16 h, images were taken using the Olympus IX70 connected to a digital camera. Images were processed using the ImageJ64 software. The area of the cell-free wound was assessed in triplicate samples. Experiments were repeated twice.
Immunofluorescence and Western Blot
immunoflurescence staining on brain tumor tissue microarrays were performed as previously describedS17 Immunofluorescence microscopy was performed on cells fixed with 4% para-formaldehyde (PFA) in phosphate buffer. Cells were permeabilized using 0.2% Triton X 100. Antibodies and concentrations used in immunofluorescence staining are:
Secondary antibodies conjugated to Alexa Fluor 594 (Molecular Probes) were used. DNA was stained by DAPI (Sigma). Fluorescence microscopy was performed on a Nikon A1R MP microscope.
Western blot analysis of U87 cells transduced with pLOC-GFP or pLOC CTNND2 was performed using the following antibodies:
Cloning and Lentiviral Production
The lentiviral expression vector, pLOC-GFP and pLOC-LZTR1 were purchased from Open Biosystems. The full length EGFR-SEPT14 cDNA was amplified from tumor sample TCGA-27-1837. Primers used were: EGFR FW: 5′-agcgATGCGACCCTCCGGGA-3′ (SEQ ID NO: 30) and SEPT14 REV: 5′-TCTTACGATGTTTGTCTTTCTTTGT (SEQ ID NO: 31); EGFR wild type, EGFR Viii and EGFR-SEPT14 cDNAs were cloned into pLoc and lentiviral particles were produced using published protocolsS13-S15.
Genomic and mRNA RT-PCR
Total RNA was extracted from cells by using RNeasy Mini Kit (QIAGEN), following the manufacturer instructions. 500 ng of total RNA was retro-transcribed by using the Superscript III kit (Invitrogen), following the manufacturer instructions. The cDNAs obtained after the retro-transcription was used as templates for qPCR as describedS13,S15. The reaction was performed with a Roche480 thermal cycler, using the Absolute Blue QPCR SYBR Green Mix from Thermo Scientific. The relative amount of specific mRNA was normalized to GAPDH. Results are presented as the mean±SD of triplicate amplifications. The validation of fusion transcripts was performed using both genomic and RT-PCR with forward and reverse primer combinations designed within the margins of the paired-end read sequences detected by RNA-seq. Expressed fusion transcript variants were subjected to direct sequencing to confirm sequence and translation frame. Primers used for the screening of gene fusions are:
Primers used for genomic detection of gene fusions are:
Subcutaneous Xenografts and Drug Treatment
Female athymic mice (nu/nu genotype, Balb/c background, 6 to 8 weeks old) were used for all antitumor studies. Patient-derived adult human glioblastoma xenografts were maintained. Xenografts were excised from host mice under sterile conditions, homogenized with the use of a tissue press/modified tissue cytosieve (Biowhitter Inc, Walkersville, Md.) and tumor homogenate was loaded into a repeating Hamilton syringe (Hamilton, Co., Reno, Nev.) dispenser. Cells were injected sub-cutaneously into the right flank of the athymic mouse at an inoculation volume of 50 μl with a 19-gauge needleS16. Subcutaneous tumors were measured twice weekly with hand-held vernier calipers (Scientific Products, McGraw, Ill.). Tumor volumes, V were calculated with the following formula: [(width)×(length)]/2=V (mm3) For the sub-cutaneously tumor studies, groups of mice randomly selected by tumor volume were treated with EGFR kinase inhibitors when the median tumor volumes were on average 150 mm3 and were compared with control animals receiving vehicle (saline). Erlotinib was administered at 100 mg/Kg orally daily for 10 days. Lapatinib was administered at 75 mg/Kg orally twice per day for 20 days. Response to treatment was assessed by delay in tumor growth and tumor regression. Growth delay, expressed as T-C, is defined as the difference in days between the median time required for tumors in treated and control animals to reach a volume five times greater than that measured at the start of the treatment. Tumor regression is defined as a decrease in tumor volume over two successive measurements. Statistical analysis was performed using a SAS statistical analysis program, the Wilcoxon rank order test for growth delay, and Fisher's exact test for tumor regression as previously described.
Glioblastoma remains one of the most challenging forms of cancer to treat. This example discusses a computational platform that integrates the analysis of copy number variations and somatic mutations and unravels the landscape of in frame gene fusions in glioblastoma. Mutations were found with loss of heterozygosity of LZTR-1, an adaptor of Cul3-containing E3 ligase complexes. Mutations and deletions disrupt LZTR-1 function, which restrains self-renewal and growth of glioma spheres retaining stem cell features. Loss-of-function mutations of CTNND2 target a neural-specific gene and are associated with transformation of glioma cells along the very aggressive mesenchymal phenotype. Recurrent translocations are reported that fuse the coding sequence of EGFR to several partners, with EGFR-SEPT14 as the most frequent functional gene fusion in human glioblastoma. EGFR-SEPT14 fusions activate Stat3 signaling and confer mitogen independency and sensitivity to EGFR inhibition. These results provide important insights into the pathogenesis of glioblastoma and highlight new targets for therapeutic intervention.
Glioblastoma (GBM) is the most common primary intrinsic malignant brain tumor affecting ˜10,000 new patients each year with a median survival rate of 12-15 months1,2. Identifying and understanding the functional significance of genetic alterations that drive initiation and progression of GBM is crucial to develop effective therapies. Previous efforts in GBM genome characterization identified somatic changes in well-known GBM genes (EGFR, PTEN, IDH1, TP53, NF1, etc.) and nominated putative cancer genes with somatic mutations, but the functional consequence of most alterations is unknown3-6. Furthermore, the abundance of passenger mutations and large regions of copy number variations (CNVs) complicates the definition of the landscape of driver mutations in glioblastoma. To address this challenge, a statistical approach was used to nominate driver genes in GBM by integrating somatic mutations identified by whole-exome sequencing with a CNVs analysis that prioritizes focality and magnitude of the genetic alterations.
Recurrent and oncogenic gene fusions are hallmarks of hematological malignancies and have also been uncovered in solid tumors7,8. Recently, a small subset of GBM harbor FGFR-TACC gene fusions was reported indicating that the patients with FGFR-TACC-positive tumors would benefit from targeted FGFR kinase inhibition9. It remains unknown whether gene fusions involving other RTK-coding genes exist and produce oncogene addiction in GBM. Here, a large RNA-sequencing dataset of primary GBM and Glioma Sphere Cultures (GSCs) is investigated and the global landscape of in frame gene fusions in human GBM are reported.
Nomination of Candidate GBM Genes
Without being bound by theory, integration of somatic point mutations and focal CNVs will uncover candidate driver GBM genes. MutComFocal is an algorithm designed to rank genes by an integrated recurrence, focality and mutation score (see Methods). This strategy was applied to 139 GBM and matched normal DNA analyzed by whole-exome sequencing to identify somatic mutations and 469 GBM analyzed by the Affymetrix SNP6.0 platform to identify CNVs.
The whole-exome analysis revealed a mean of 43 nonsynonymous somatic mutations per tumor sample. The distribution of substitutions shows a higher rate of transitions versus tranversions (67%), with a strong preference for C→T and G→A (55%) (
A list of 67 genes were generated that score at the top of each of the three categories and included nearly all the genes previously implicated in GBM. Among these genes, (labeled in light grey in
Among the commonly mutated and focally deleted genes exhibiting top MutComFocal scores and validated in the independent GBM dataset, BCOR, LRP family members, HERC2, LZTR-1 and CTNND2. BCOR, an X-linked gene, encodes for a component of the nuclear co-repressor complex that is essential for normal development of neuroectoderm and stem cell functions11-13. BCOR mutations have recently been described in retinoblastoma and medulloblastoma14,15. LRP1B, a member of the LDL receptor family, is among the most frequently mutated genes in human cancer (
LZTR-1 Mutations Inactivate a Cullin-3 Adaptor to Drive Self-Renewal and Growth of Glioma Spheres
A gene that received one of the highest Del-Mut score by MutComFocal is LZTR-1 (
LZTR-1 codes for a protein with a characteristic Kelch-BTB-BACK-BTB-BACK domain architecture (
To address the function of LZTR-1 mutants, a homology model of LZTR-1 was built based partly on the crystal structures of the MATH-BTB-BACK protein SPOP26, the BTB-BACK-Kelch proteins KLHL327 and KLHL1128, and the Kelch domain of Keap129 (
The R198G and G248R mutations localize to the b-c loop of the Kelch domain, in a region predicted to provide the substrate-binding surface29. The W105R mutation targets a highly conserved anchor residue in the Kelch repeats and the T288I mutation disrupts a buried residue conserved in LZTR-1 (
To ask whether the mutations predicted to affect the BTB-BACK domains perturb the interaction with Cul3, in vitro translated wild type, E353STOP, W437STOP and R810W LZTR-1 Myc-tagged proteins were prepared and their ability to bind to Flag-Cul3 purified from mammalian cells was tested. Wild type LZTR-1 bound Flag-Cul3, but the E353STOP and W437STOP mutants lost this property. However, the R810W mutant retained Cul3 binding in this assay (
Next, the biological consequences of LZTR-1 inactivation in human GBM. Differential gene expression pattern of GBM harboring mutations was examined and deletions of LZTR-1 or normal LZTR-1 revealed that tumors with genetic inactivation of LZTR-1 were enriched for genes associated with glioma sphere growth and proliferation35 (
Inactivation of CTNND2 Induces Mesenchymal Transformation in Glioblastoma
Among the top ranking genes in MutComFocal, CTNND2 is expressed at the highest levels in normal brain. CTNND2 codes for δ-catenin, a member of the p120 subfamily of catenins expressed almost exclusively in the nervous system where it is crucial for neurite elongation, dendritic morphogenesis and synaptic plasticity36-38. Germ-line hemizygous loss of CTNND2 impairs cognitive functions and underlies some forms of mental retardation39,40. CTNND2 shows pronounced clustering of mutations in GBM. The observed spectrum of mutations includes four mutations in the armadillo-coding domain and one in the region coding for the N-terminal coiled-coil domain (
Immunostaining experiments showed that δ-catenin is strongly expressed in normal brain, particularly in neurons, as demonstrated by co-staining with the neuronal markers β3-tubulin and MAP2 but not the astrocytic marker GFAP (
Mesenchymal transformation of GBM is associated with irreversible loss of proneural cell fate and neuronal markers42 and is detected in most established glioma cell lines. Expression of δcatenin in the U87 human glioma cell line reduced cell proliferation (
Next, the effect of expressing δ-catenin in GBM-derived sphere culture #48 that lacks the endogenous δ-catenin protein (
Recurrent EGFR Fusions in GBM
To identify gene fusions in GBM, RNA-seq data was analyzed from a total of 185 GBM samples (161 primary GBM plus 24 short-term glioma sphere cultures freshly isolated from patients carrying primary GBM). The analysis of RNA-seq led to the discovery of 92 candidate rearrangements giving rise to in-frame fusion transcripts (Table 7). Besides previously reported FGFR3-TACC3 fusions events, the most frequent recurrent in-frame fusions involved EGFR in 7.6% of samples (14/185, 3.8%-11.3% CI). Nine of 14 EGFR fusions included recurrent partners SEPT14 (6/185, 3.2%) and PSPH (3/185, 1.6%) as the 3′ gene segment in the fusion. All EGFR-SEPT14 and two of three EGFR-PSPH gene fusions occurred within amplified regions of the fusion genes (
The quantitative analysis of expressed reads spanning the fusion breakpoint versus reads spanning EGFR exons not implicated in the fusion transcripts revealed that EGFR fusion genes were expressed at higher levels in five of nine tumors (Table 11). Two in-frame highly expressed fusions involving the neurotrophic tyrosine kinase receptor 1 gene (NTRK1) as the 3′ gene with two different 5′ partners (NFASC-NTRK1 and BCAN-NTRK1). Fusions involving NTRK1 are common in papillary thyroid carcinomas44. Using EXomeFuse, an algorithm that reconstructs genomic fusions from whole-exome data, EGFR-SEPT14 and NRTK1 fusions result from recurrent chromosomal translocations and the corresponding genomic breakpoints were reconstructed (Table 12).
The sequence of the PCR products spanning the fusion breakpoint validated all three types of recurrent in frame fusion predictions (EGFR-SEPT14, EGFR-PSPH and NRTK1 fusions,
Using PCR, the genomic breakpoint was mapped to chromosome 7 (#55,268,937 for EGFR and #55,870,909 for SEPT14, genome build GRCh37/hg19) within EGFR exon 25 and SEPT14 intron 9, creating a transcript in which the 5′ EGFR exon 24 is spliced to the 3′ SEPT14 exon 10 (
To confirm that GBM harbors recurrent EGFR fusions and determine the frequency in an independent dataset, cDNA was screened from a panel of 248 GBMs and discovered 10 additional cases with EGFR-SEPT14 fusions (4%). Conversely, NFASC-NTRK1 fusions were not detected in this dataset. A 2.2% (3/135) frequency of EGFR-PSPH fusions was determined.
The discovery of recurrent EGFR fusions in GBM is of particular interest. EGFR is activated in a significant fraction of primary GBM (˜25%) by an in-frame deletion of exons 2-7 (EGFRvIII)45. However, seven of nine tumors harboring EGFR-SEPT14 and EGFR-PSPH gene fusions lacked the EGFRvIII rearrangement (Table 13). It was determined whether the most frequent EGFR fusion in GBM (EGFR-SEPT14) provides an alternative mechanism of EGFR activation and confers sensitivity to EGFR inhibition. First, whether EGFR gene fusions cluster into any gene expression subtype of GBM (proneural, neural, classical, mesenchymal) was investigated. Although no individual subtype displayed a statistically significant enrichment of EGFR fusions, 8 of 9 GBM harboring EGFR-SEPT14 or EGFR-PSPH belonged to the classical or mesenchymal subtype (Fisher's P value=0.05 for classical/mesenchymal enrichment, Table 14).
Next, the effects of ectopic EGFR-SEPT14, EGFRvIII or EGFR wild type on glioma cells were investigated. Lentiviral transduction of #48 human glioma sphere culture (which lacks genomic alteration of EGFR) showed that cells expressing EGFR-SEPT14 or EGFRvIII but not those expressing wild type EGFR or vector retained growth and self-renewal in the absence of EGF and bFGF (
Finally, it was investigated whether EGFR-SEPT14 fusions confer sensitivity to inhibition of EGFR-TK. Treatment of #48 expressing EGFR-SEPT14, EGFRvIII, wild type EGFR or vector control with lapatinib, an irreversible EGFR inhibitor recently proposed to target EGFR alterations in GBM47, revealed that EGFR-Sept14 and EGFRvIII but not wild-type EGFR sensitized glioma cells to pharmaceutical EGFR inhibition (
To ask whether sensitivity to EGFR-TK inhibition is retained in human glioma cells naturally harboring EGFR-SEPT14 in vivo, an EGFR-SEPT14-positive GBM xenograft (D08-0537 MG) established from a heavily pretreated patient was used. Treatment of D08-0537 MG tumors with lapatinib or erlotinib showed that both drugs significantly delayed tumor growth, with lapatinib displaying the strongest anti-tumor effects. Conversely, EGFR inhibitors were ineffective against GBM xenograft D08-0714 MG, which lacks EGFR genomic alterations (
Discussion
A computational pipeline was described that computes frequency, magnitude and focality of CNVs at any loci in the human genome with the somatic mutation rate for genes residing at that genomic location, thus integrating into a single score two genetic hallmarks of driver cancer genes (focality of CNVs and point mutations). Besides recognizing nearly all genes known to have functional relevance in GBM, this study discovered and validated somatic mutations in 18 new genes, which also harbor focal and recurrent CNVs in a significant fraction of GBM. The importance of some of these genes extends beyond GBM, as underscored by cross-tumor relevance (e.g. BCOR), and protein family recurrence (e.g. LRP family members).
Also, the LZTR-1 mutations targeting highly conserved residues in the Kelch domain (W105, G248, T288) and in the second BTB-BACK domain (R810) are recurrent events in other tumor types48. Thus, understanding the nature of substrates of LZTR-1-Cul3 ubiquitin ligase activity will provide important insights into the pathogenesis of multiple cancer types. The importance of LZTR-1 genetic alterations in GBM is underscored by concurrent targeting of LZTR-1 by mutations and deletions that supports a two-hits mechanism of tumor suppressor gene inactivation as well as the impact of mutations targeting the BTB-BACK domains on Cul3 binding and/or protein stability, and their ability to release glioma cells from the restraining activity of the wild-type protein on self-renewal.
The finding that loss-of-function of CTNND2 cluster in mesenchymal GBM provides a clue to the genetic events driving this aggressive GBM subtype. The function of 8-catenin for crucial neuronal morphogenesis indicates that full-blown mesenchymal transformation in the brain requires loss of master regulators constraining cell determination along the neuronal lineage. Introduction of δ-catenin in human glioma spheres collapsed the mesenchymal phenotype and inhibited sphere formation and tumor growth. Thus, the ability of δ-catenin to reprogram glioma cells expressing mesenchymal genes towards a neuronal fate unravels an unexpected plasticity of mesenchymal GBM that might be exploited therapeutically.
In this study, the landscape of gene fusions from a large dataset of GBM analyzed by RNA-Sequencing is also reported. In-frame gene fusions retaining the RTK-coding domain of EGFR emerged as the most frequent gene fusion in GBM. In this tumor, EGFR is frequently targeted by focal amplications and our finding underscores the strong recombinogenic probability of focally amplified genes, as recently reported for the myc locus in medulloblastoma49. Resembling intragenic rearrangements that generate the EGFRvIII allele, EGFR-SEPT14 fusions impart to glioma cells the ability to self-renew and grow in the absence of mitogens, constitutively activate STAT3 signaling, and confer sensitivity to EGFR inhibition. These findings highlight the relevance of fusions implicating RTK-coding genes in the pathogenesis of GBM9. They also provide a strong rationale for the inclusion of GBM patients harboring EGFR fusions in clinical trials based on EGFR inhibitors.
Methods
SAVI (Statistical Algorithm for Variant Frequency Identification).
The frequencies of variant alleles were estimated in 139 paired tumor and normal whole-exome samples from TCGA using the SAVI pipeline50. The algorithm estimates the frequency of variant alleles by constructing an empirical Bayesian prior for those frequencies, using data from the whole sample, and obtains a posterior distribution and high credibility intervals for each allele50. The prior and posterior are distributed over a discrete set of frequencies with a precision of 1% and are connected by a modified binomial likelihood, which allows for some error rate. More precisely, a prior distribution p(f) of the frequency f and a prior for the error e uniform on the interval [0,E] for a fixed 0≦E≦1 is assumed. The sequencing data at a particular allele is a random experiment producing a string of m (the total depth at the allele) bits with n ‘1’s (the variant depth at the allele). Assuming a binomial likelihood of the data and allowing for bits being misread because of random errors, the posterior probability P(f) of the frequency f is
where C is a normalization constant. For a particular allele, the value of E is determined by the quality of the nucleotides sequenced at that position as specified by their Phred scores. The SAVI pipeline takes as input the reads produced by the sequencing technology, filters out low-quality reads and maps the rest onto a human reference genome. After mapping, a Bayesian prior for the distribution of allele frequencies for each sample is constructed by an iterative posterior update procedure starting with a uniform prior. To genotype the sample, the posterior high-credibility intervals were used for the frequency of the alleles at each genomic location. Alternatively, combining the Bayesian priors from different samples, posterior high-credibility intervals were obtained for the difference between the samples of the frequencies of each allele. Finally, the statistically significant differences between the tumor and normal samples are reported as somatic variants. To estimate the positive prediction value of SAVI in the TCGA GBM samples, 41 mutations were selected for independent validation by Sanger sequencing. 39 of the 41 mutations using Sanger sequencing were confirmed, resulting in a 0.95 (95% CI 0.83-0.99) validation rate.
Candidate genes were ranked by the number of somatic nonsynonymous mutations. A robust fit of the ratio of nonsynonymous to synonymous mutations was generated with a bisquare weighting function. The excess of nonsynonymous alterations was estimated using a Poisson distribution with a mean equal to the product of the ratio from the robust fit and the number of synonymous mutations. Genes in highly polymorphic genomic regions were filtered out based on an independent cohort of normal samples. The list of these regions includes families of genes known to generate false positives in somatic predictions (for example, the HLA, KRT and OR gene families).
MutComFocal.
Key cancer genes are often amplified or deleted in chromosomal regions containing many other genes. Point mutations and gene fusions, conversely, provide more specific information about which genes may be implicated in the oncogenic process. MutComFocal was developed, a Bayesian approach that assigns a driver score to each gene by integrating point mutations and CNV data from 469 GBMs (Affymetrix SNP6.0). In general, MutComFocal uses three different strategies. First, the focality component of the score is inversely proportional to the size of the genomic lesion to which a gene belongs and thus prioritizes more focal genomic lesions. Second, the recurrence component of the MutComFocal score is inversely proportional to the total number of genes altered in a sample, which prioritizes samples with a smaller number of altered genes. Third, the mutation component of the score is inversely proportional to the total number of genes mutated in a sample, which achieves the twofold goal of prioritizing mutated genes on one hand and prioritizing samples with a smaller number of mutations on the other.
More specifically, for a particular sample, let (c1, N1), . . . , (ck, Nk) describe the amplification lesions in that sample so that N1 is the number of genes in the ith lesion and c1 is its copy number change from normal. For a gene belonging to the ith lesion, the amplification recurrence sample score is defined as (c1, N1), . . . , (ck, Nk), and its amplification focality sample score is defined as (ci/Σjcj)×(1/Ni). To obtain the amplification recurrence and focality scores for a particular gene, the corresponding sample scores were summed over all the samples and the result was normalized so that each score sums to 1. The deletion and recurrence scores are defined in a similar manner. The mutation score is analogous to a recurrence score in which it is assumed that mutated genes belong to lesions with only one gene.
The amplification/mutation score is defined as the product of the two amplification scores and the mutation score, whereas the deletion/mutation score is defined as the product of the two deletion scores and the mutation score. The amplification/mutation and deletion/mutation scores are normalized to 1, and for each score, genes are divided into tiers iteratively so that the top 2X remaining genes are included in the next tier, where H is the entropy of the scores of the remaining genes normalized to 1. On the basis of their tier across the different types of scores, genes are assigned to being either deleted/mutated or amplified/mutated, and genes in the top tiers are grouped into contiguous regions. The top genes in each region are considered manually and selected for further functional validation.
The recurrence and focality scores can be interpreted as the posterior probabilities that a gene is driving the selection of the disease under two different priors, one global and one local in nature. The recurrence score is higher if a gene participates in many samples that do not have too many altered genes, whereas the focality score is higher if the gene participates in many focal lesions. Besides lending strong support to the inference of a gene as a potential driver, the directionality of the copy number alteration (amplification or deletion) informs the probable behavior of the candidate gene as an oncogene or tumor suppressor, respectively.
The genes displayed in
RNA-Seq Bioinformatics Analysis.
161 RNA-seq GBM tumor samples were analyzed from TCGA, a public repository containing large-scale genome sequencing of different cancers, plus 24 patient-derived GSCs. Nine GSC samples reported in previous studies were kept in our analysis to evaluate recurrence9. The samples were analyzed using the ChimeraScan51 algorithm to detect a list of gene fusion candidates. Briefly, ChimeraScan detects those reads that discordantly align to different transcripts of the same reference (split inserts). These reads provide an initial set of putative fusion candidates. The algorithm then realigns the initially unmapped reads to the putative fusion candidates and detects those reads that align across the junction boundary (split reads). These reads provide the genomic coordinates of the breakpoint.
RNA-seq analysis detected a total of 39,329 putative gene fusion events. To focus the experimental analysis on biologically relevant fused transcripts, the Pegasus annotation pipeline (http://sourceforge.net/projects/pegasus-fus/) was applied. For each putative fusion, Pegasus reconstructs the entire fusion sequence on the basis of the genomic fusion breakpoint coordinates and gene annotations. Pegasus also annotates the reading frame of the resulting fusion sequences as either in frame or a frame shift. Moreover, Pegasus detects the protein domains that are either conserved or lost in the new chimeric event by predicting the amino acid sequence and automatically querying the UniProt web service. On the basis of the Pegasus annotation report, relevant gene fusions were selected for further experimental validation according to the reading frame and the conserved and lost domains. The selected list was based on in-frame events expressed by ten or more reads, with at least one read spanning the breaking point. To filter out candidate trans-splicing events, events with putative breakpoints at a distance of at least 25 kb were pursued.
Identification of Genetic Rearrangements Using Whole-Exome Data.
Although whole-exome sequencing data contain low intronic coverage that reduces the sensitivity for fusion discovery, they are readily available through the TCGA database. To characterize the genomic breakpoint of the chromosomal rearrangement, EXome-Fuse, a new gene fusion discovery pipeline that is designed particularly to analyze whole-exome data, was designed. For the samples harboring EGFR-SEPT14, EGFR-PSPH, NFASC-NTRK1 and BCAN-NTRK1 fusions in RNA, EXome-Fuse was applied to the corresponding whole-exome sequencing data deposited in TCGA. This algorithm can be divided into three stages: split-insert identification, split-read identification and virtual reference alignment. Mapping against the human genome reference hg18 with BWA, all split inserts are first identified to compile a preliminary list of fusion candidates. This list was pruned of any false positives produced from paralogous gene pairs using the Duplicated Genes Database and the EnsemblCompara GeneTrees52. Pseudogenes in the candidate list were annotated using the list from the HUGO Gene Nomenclature Committee (HGNC) database53 and were given lower priority. Candidates were also filtered out between homologous genes, as well as those with homologous or low-complexity regions around the breakpoint. For the remaining fusion candidates, any supporting split reads were probed for and their mates using BLAST with a word size of 16, identity cutoff of 90% and an expectation cutoff of 10−4. A virtual reference was created for each fusion transcript and all reads were realigned to calculate a final tally of split inserts and split reads such that all aligning read pairs maintain forward-reverse directionality.
Targeted Exon Sequencing.
All protein-coding exons for the 24 genes of interest were sequenced using genomic DNA extracted from frozen tumors and matched blood. Five-hundred nanograms of DNA from each sample were sheared to an average size of 150 bp in a Covaris instrument for 360 s (duty cycle, 10%; intensity, 5; cycles per burst, 200). Bar-coded libraries were prepared using the Kapa High-Throughput Library Preparation Kit Standard (Kapa Biosystems). Libraries were amplified using the KAPA HiFi Library Amplification kit (Kapa Biosystems) (eight cycles). Libraries were quantified using Qubit Fluorimetric Quantitation (Invitrogen), and the quality and size was assessed using an Agilent Bioanalyzer. An equimolar pool of the four bar-coded libraries (300 ng each) was created, and 1,200 ng was input to exon capture using one reaction tube of the custom Nimblegen SeqCap EZ (Roche) with custom probes targeting the coding exons of the 38 genes. Capture by hybridization was performed according to the manufacturer's protocols with the following modifications: 1 nmol of a pool of blocker oligonucleotides (complementary to the bar-coded adapters) was used, and post-capture PCR amplification was done using the KAPA HiFi Library Amplification kit, instead of the Phusion High-Fidelity PCR Master Mix with HF Buffer Kit, in a 60 μl volume, as the Kapa HiFi kit greatly reduced or eliminated the bias against GC-rich regions.
The pooled capture library was quantified by Qubit (Invitrogen) and Bioanalyzer (Agilent) and sequenced in on an Illumina MiSeq sequencer using the 2×150 paired-end cycle protocol. Reads were aligned to the hg19 build of the human genome using BWA with duplicate removal using SAMtools as implemented by Illumina MiSeq Reporter. Variant detection was performed using GATK UnifiedGenotyper. Somatic mutations were identified for paired samples using SomaticSniper and filtered for frequency of less than 3% in normal samples and over 3% in tumor samples. Variants were annotated with the Charity annotator to identify protein-coding changes and cross referenced against known dbSNP, 1000 Genomes and COSMIC variants. Sanger sequencing was used to confirm each mutation from normal and tumor DNA.
Enrichment of Amplified and Deleted Genes for Single-Nucleotide Variants (SNVs).
Although MutComFocal combines SNV and CNV data to identify genes driving oncogenesis, it does not explicitly determine whether amplified or deleted genes are enriched for SNVs within the same sample. Deletions and SNVs of a gene within the same sample might indicate a two-hit model of a tumor suppressor. Alternatively, amplifications and gain-of-function mutations of an oncogene within the sample might further promote oncogenesis. For each MutComFocal candidate gene, the number of TCGA samples was determined with both amplification and SNVs, amplification alone, SNVs alone or neither. The corresponding Fisher's P value was calculated. A similar analysis for deletions was performed.
Correlation Between Copy Number and Expression.
One method of assessing the functional relevance of an amplified or deleted gene is to assess the effect of gene dosage. For each gene nominated by MutComFocal, the Pearson's correlation coefficient was calculated between copy number and expression. The corresponding P values were computed using paired Student's t test.
Allele-Specific Expression of SNVs.
For a given gene nominated by MutComFocal, RNA sequencing can determine whether the mutant or wild-type allele is expressed. Toward this end, VCFtools54 was applied to the TCGA BAM RNA-seq files produced by TopHat, which produces the depth of reads calling the reference (R) and variant (V) allele. A measure of relative expression of the variant allele is then V/(V+R). For each mutation, the binomial P value of observing more than V out of V+R reads was calculated, assuming that it is equally probable for a read to call the variant or reference. The binomial P values of each mutation were then pooled using the Stouffer's Z-score method to calculate the combined P value per gene.
Ruling Out Passenger Mutations in Hypermutated Samples.
To rule out the possibility that MutComFocal candidates tend to be passenger mutations in hypermutated samples, the number of mutations was compared in samples harboring a MutComFocal mutation to the distribution N of the number of mutations in each TCGA sample. Because the number of TCGA samples was well above 30, N was assummed to be well approximated by the normal distribution and calculated the mean, μ, and s.d., σ. For each MutComFocal mutation, the Z-test was performed and all mutations failed statistical significance after correction by the Benjamini-Hochberg method.
Determining the Presence of EGFRvIII Transcripts.
To determine the prevalence of EGFRvIII transcripts, an in-house script was created to calculate the number of split inserts and split reads supporting the junction between EGFR exons 1 and 8. The EGFRvIII isoform was considered to be expressed if there were more than five split reads or five split inserts in a sample.
Calculating the Relative Expression of EGFR Fusions Compared to Wild-Type EGFR.
To determine the functional relevance of EGFR-SEPT14 and EGFR-PSPH fusions, the relative expression was determined between the fusion and wild-type transcripts within each sample on the basis of BAM files mapped by TopHat and provided by TCGA. As a proxy for expression of the transcript, the depth of reads covering either a mutant or wild-type junction was calculated. In particular, the depth of reads covering the fusion breakpoint of EGFR-SEPT14 or EGFR-PSPH was considered to estimate the expression of the fusion transcript. Because all EGFR fusions stereotypically involved exon 24 joined to either SEPT14 or PSPH, the depth of reads covering the junctions between EGFR exons 25-26, 26-27 and 27-28 to be a specific gauge of wild-type EGFR expression was assessed.
Enrichment of the Classical and Mesenchymal Subtype Among Samples with EGFR Fusions.
To assess whether samples with EGFR fusions tended to occur in a particular GBM subtype, each TCGA GBM sample was first classified by expression according to the methods of Verhaak et al.6. The number of classical, mesenchymal, proneural and neural samples was then tallied with and without EGFR gene fusions. The combined class of classical and mesenchymal phenotype was enriched for EGFR fusions according to the Fisher's exact test.
Copy Number Variation in EGFR Fusions.
Gene fusions often arise from genomic instability. Motivated by this observation, segmented SNP array data was downloaded from TCGA and calculated the log 2 ratio between the tumor and normal copy numbers. This was plotted along the chromosomal neighborhood of EGFR, SEPT14 and PSPH (chr7:55,000,000-56,500,000).
GSEA.
To determine the biological impact of LZTR1 mutations, GSEA55 was used, which is an analytical tool that harnesses expression data to nominate gene sets enriched for a particular phenotype. Having identified TCGA samples with LZTR1 SNVs, GSEA was applied to the TCGA expression data. Samples were first compared with LZTR1 SNVs against those with wild-type LZTR1 (excluding LZTR1 deletions). To assess statistical significance, the data set was randomized by permuting gene sets 500 times and considered only gene sets with an FDR q<0.05.
Differential Expression Between Samples with EGFR-SEPT14 and EGFRvIII.
In-house differential expression analysis was also performed to determine a distinct molecular signature distinguishing the EGFR-SEPT14 and EGFRvIII phenotypes. Toward this end, a t test was performed comparing the expression of the two groups of samples for each gene. Correcting using the Benjamini-Hochberg method, only genes with FDR<0.05 were considered. In addition, genes were excluded with a variance less than the tenth percentile or absolute value lower than two across all samples. These filters left a predictive set of ten genes. Hierarchical clustering was then performed on the expression of these ten genes using Euclidean distance and average linkage.
Modeling of LZTR1.
Structural templates for the kelch and BTB-BACK regions of human LZTR1 were identified with HHpred56. An initial three-dimensional model was generated with the I-TASSER server57. The CUL3 N-terminal domain was docked onto the model by superposing the KLHL3BTB-BACK/CUL3NTD crystal structure27 onto the second LZTR1 BTB-BACK domain. The model does not include higher quaternary structure, although many BTB domains, and many kelch domains, are known to self associate25. The short linkage between the end of the first BACK domain and the beginning of the second BTB domain would seem to preclude an intrachain BTB-BTB pseudo-homodimer, and without being bond by theory, LZTR1 should self associate and form higher-order assemblies. Both BACK domains are the shorter, atypical form of the domain and consist of two helical hairpin motifs, as in SPOP26,58, and not the four-hairpin motif seen in most BTB-BACK-kelch proteins28,58. The model from the kelch domain predicts an unusual 1+3 velcro arrangement59, with the N-terminal region contributing strand d of blade 1 and the C-terminal region contributing strands a, b and c of the same blade, although an alternative 2+2 velcro model cannot be ruled out.
Cell Culture.
U87 cells were obtained from ATCC. SNB19, U87 and HEK-293T cells were cultured in DMEM supplemented with 10% fetal bovine serum (FBS). Growth rates were determined by plating cells in six-well plates at 3 d after infection with the lentivirus indicated in the figure legends. The number of viable cells was determined by Trypan blue exclusion in triplicate cultures obtained from triplicate independent infections. For the wound assay testing migration, confluent cells were scratched with a pipette tip and cultured in 0.25% FBS. After 16 h, images were taken using the Olympus IX70 connected to a digital camera. Images were processed using the ImageJ64 software. The area of the cell-free wound was assessed in triplicate samples. Experiments were repeated twice.
GBM-derived primary cultures were grown in DMEM:F12 medium containing N2 and B27 supplements and human recombinant FGF-2 and EGF (50 ng/ml each; Peprotech). For sphere formation, cells were infected with lentiviral particles. Four days later, single cells were plated at density of 1 cells per well in triplicate in low-attachment 96-well plates. The number and the size of spheres were scored after 10-14 d. Limiting dilution assays were performed as described previously60. Spheres were dissociated into single cells and plated in low-attachment 96-well plates in 0.2 ml of medium containing growth factors (EGF and FGF-2), except for the EGFR-transduced cells, which were cultured in the absence of EGF. Cultures were left undisturbed for 10 d, and then the percentage of wells not containing spheres for each cell dilution was calculated and plotted against the number of cells per well. Linear regression lines were plotted, and the number of cells required to generate at least one sphere in every well (the stem cell frequency) was calculated. The experiment was repeated twice. Treatment of GBM primary cultures with erlotinib or lapatinib was performed in cells transduced with the pLOC vector, wild-type pLOC-EGFR, EGFRvIII or EGFR-SEPT14 and selected with blasticidin for 5 d. Cells were seeded on 6-cm dishes in the absence of EGF and treated with the indicated drugs at the indicated doses for 48 h. Each treatment group was seeded in triplicate. Absolute viable cell counts were determined by Trypan blue exclusion and counted on a hemocytometer. EGF stimulation of EGFR-transduced primary glioma cells was performed in cells deprived of growth factors for 48 h. Cells were collected at the indicated times and processed for protein blot analysis.
Immunofluorescence.
Immunofluorescence staining on normal mouse and human brain and brain tumor tissue microarrays were performed as previously described43,61,62. Immunofluorescence microscopy was performed on cells fixed with 4% paraformaldehyde in phosphate buffer. Cells were permeabilized using 0.2% Triton X-100. The antibodies and concentrations used in the immunofluorescence staining are detailed in Table 15.
Secondary antibodies conjugated to Alexa Fluor 594 (1:300, A11037, Molecular Probes) or Alexa 488 (1:500, A11008, Molecular Probes) were used. DNA was stained with DAPI (Sigma). Fluorescence microscopy was performed on a Nikon A1R MP microscope. Quantification of the fluorescence intensity staining in primary or established glioma cells was performed using NIH ImageJ software (see URLs). A histogram of the intensity of fluorescence of each point of a representative field for each condition was generated. The fluorescence intensity of ten fields from three independent experiments was scored, standardized to the number of cells in the field and divided by the intensity of the vector.
Protein Blotting, Immunoprecipitation and In Vitro Binding.
Protein blot analysis and immunoprecipitation were performed using the antibodies detailed in Table 16. For the in vitro binding between CUL3 and LZTR1, wild-type and mutant LZTR1 were translated in vitro using the TNT Quick Coupled Transcription/Translation System (Promega). Flag-CUL3 was immunoprecipitated from transfected HEK-293T cells with Flag-M2 beads (Sigma) using RIPA buffer (50 mM Tris-HCl, pH 7.5, 150 mM NaCl, 1% NP-40, 0.5% sodium deoxycholate (DOC), 0.1% SDS, 1 mM phenylmethylsulfonyl fluoride (PMSF), 10 mM NaF, 0.5 M Na3OV4 (sodium orthovanadate) and Complete Protease Inhibitor Cocktail, Roche). Binding was performed in 200 mM NaCl plus 0.5% NP-40 for 2 h at 4° C. Immunocomplexes were analyzed by SDS-PAGE and immunoblot.
Cloning and Lentiviral Production.
The lentiviral expression vectors pLOC-GFP and pLOC-CTNND2 were purchased from Open Biosystems. Full-length EGFR-SEPT14 cDNA was amplified from tumor sample TCGA-27-1837. Wild-type EGFR, EGFRvIII and EGFR-SEPT14 cDNAs were cloned into the pLOC vector. pCDNA-MYC-Hist-LZTR1 was a kind gift24. pCDNA-Flag-CUL3 was a gift. Wild-type and mutant cDNAs for LZTR1 and CTNND2 obtained by site-directed mutagenesis (QuikChange II, Agilent) were cloned into the pLOC vector. Lentiviral particles were produced using published protocols43, 61, 62, 63, 64.
Genomic PCR and RT-PCR.
Total RNA was extracted from cells using an RNeasy Mini Kit (QIAGEN) following the manufacturer's instructions. Five-hundred nanograms of total RNA was retrotranscribed using the Superscript III kit (Invitrogen) following the manufacturer's instructions. The cDNAs obtained after the retrotranscription were used as templates for quantitative PCR as described43,64. The reaction was performed with a Roche480 thermal cycler using the Absolute Blue QPCR SYBR Green Mix from Thermo Scientific. The relative amount of specific mRNA was normalized to GAPDH. Results are presented as the mean±s.d. of triplicate amplifications. The validation of fusion transcripts was performed using both genomic PCR and RT-PCR with forward and reverse primer combinations designed within the margins of the paired-end read sequences detected by RNA-seq. Expressed fusion transcript variants were subjected to direct sequencing to confirm the sequence and translation frame. The primers used for the screening of gene fusions are detailed in Table 17. The primers used for genomic detection of gene fusions are listed in Table 18. Semiquantitative RT-PCR to detect exogenous wild-type MYC-LZTR1 and mutant p.Arg801Trp LZTR1 was performed using the primers listed in Table 19.
Subcutaneous Xenografts and Drug Treatment.
Female athymic mice (nu/nu genotype, BALB/c background, 6-8 weeks old) were used for all antitumor studies. Patient-derived adult human glioblastoma xenografts were maintained. Xenografts were excised from host mice under sterile conditions and homogenized with the use of a tissue press and modified tissue cytosieve (Biowhitter Inc.), and tumor homogenate was loaded into a repeating Hamilton syringe (Hamilton, Co.) dispenser. Cells were injected subcutaneously into the right flank of the athymic mouse at an inoculation volume of 50 ml with a 19-gauge needle65.
Subcutaneous tumors were measured twice weekly with hand-held vernier calipers (Scientific Products). Tumor volumes (V) were calculated with the following formula: ((width)×(length))/2=V (mm3) For the subcutaneous tumor studies, groups of mice randomly selected by tumor volume were treated with EGFR kinase inhibitors when the median tumor volumes were an average of 150 mm3 and were compared with control animals receiving vehicle (saline).
Erlotinib was administered at 100 mg per kg body weight orally once per day for 10 d. Lapatinib was administered at 75 mg per kg body weight orally twice per day for 20 d. Response to treatment was assessed by a delay in tumor growth and tumor regression.
Growth delay, expressed as a T-C value, is defined as the difference in days between the median time required for tumors in treated and control animals to reach a volume five times greater than that measured at the start of the treatment. Tumor regression is defined as a decrease in tumor volume over two successive measurements. Statistical analysis was performed using a SAS statistical analysis program, the Wilcoxon rank-order test for growth delay and Fisher's exact test for tumor regression.
Intracranial Injection.
GBM-derived primary cells were first infected with a lentivirus expressing luciferase and subsequently transduced with the pLOC vector or pLOC-CTNND2 lentiviral particles. Intracranial injection was performed in 9-week-old male nu/nu mice (Charles River Laboratories). Briefly, 5≦105 cells were resuspended in 2.5 μl of PBS and injected into the caudate putamen using a stereotaxic frame (coordinates relative to the bregma: 0.6 mm anterior; 1.65 mm medium-lateral; 3 mm depth-ventral). Tumor growth was monitored using the IVIS Imaging system. Briefly, mice were anesthetized with 3% isoflurane before intraperitoneal injection of 100 mg per kg body weight n-luciferin (Xenogen). Ten minutes after injection of n-luciferin, images were acquired for 1 min with the Xenogen IVIS system (Xenogen) using Living Image acquisition and analysis software (Xenogen). The bioluminescent signal was expressed in photons per second and displayed as a pseudo-color image representing the spatial distribution of photon counts.
URLs.
DNA and RNA sequencing and copy number variant data in The Cancer Genome Atlas (TCGA), http://cancergenome.nih.gov; glioma patient survival data from the Repository for Molecular Brain Neoplasia Data (REMBRANDT), https://caintegrator.nci.nih.gov/rembrandt/; sequence data deposition in database of Genotypes and Phenotypes (dbGaP), http://www.ncbi.nlm.nih.gov/gap; gene fusion annotation software package Pegasus, http://sourceforge.net/projects/pegasus-fus/.
Data Access.
RNA sequencing of twenty-four human GBM sphere cultures in this study were deposited under the dbGaP study accession phs000505.v2.p1. RNA and DNA sequencing of TCGA GBM samples was also analyzed from the dbGaP study accession phs000178.v1.p1.
Annotation information in each column is described below for Table 7:
sample: Name of TCGA or private sample.
#chrom5p: 5′ chromosome
#start5p: 5′ genomic start coordinate
#end5p: 5′ genomic end coordinate
#chrom3p: 3′ chromosome
#start3p: 3′ genomic start coordinate
#end3p: 3′ genomic end coordinate
strand5p: 5′ strand
strand3p: 3′ strand
genes5p: 5′ gene
genes3p: 3′ gene
total_frags (split inserts+split reads): Total number of split inserts and split reads
spanning_frags (split reads): Number of split reads
GeneBreakpoint5p: The genomic coordinate of the breakpoint in the 5′ gene
GeneBreakpoint3p: The genomic coordinate of the breakpoint in the 3′ gene
FrameType: Reading frame of gene fusions. Values include in-frame, frameshift, or null (no transcript information was found in the Ensembl Homo_sapiens.GRCh37.60.gtf file).
FusedSequence: Reconstructed sequence of the fusion RNA transcript
ProteinStart5p: The start coordinate of the 5′ protein segment
ProteinStop5p: The stop coordinate (breakpoint) of the 5′ protein segment
ProteinStart3p: The start coordinate (breakpoint) of the 3′ protein segment
ProteinStop3p: The stop coordinate of the 3′ protein segment
ProteinSequence: Reconstructed sequence of the fusion protein
ExonBreak5p: The last exon of the 5′ gene before the breakpoint
ExonBreak3p: The first exon of the 3′ gene after the breakpoint
Table 8. Genomic breakpoints of gene fusions detected through whole-exome DNA sequencing. Annotation information in each column is described below:
Table 8. Genomic breakpoints of gene fusions detected through whole-exome DNA sequencing. Annotation information in each column is described below:
The application is a continuation of PCT International Application No. PCT/US2014/026351 filed on Mar. 13, 2014, which claims the benefit of and priority to U.S. Provisional Patent Application No. 61/793,086, filed on Mar. 15, 2013, the content of which are hereby incorporated by reference in their entireties. All patents, patent applications and publications cited herein are hereby incorporated by reference in their entirety. The disclosures of these publications in their entireties are hereby incorporated by reference into this application. This patent disclosure contains material that is subject to copyright protection. The copyright owner has no objection to the facsimile reproduction by anyone of the patent document or the patent disclosure as it appears in the U.S. Patent and Trademark Office patent file or records, but otherwise reserves any and all copyright rights.
This invention was made with government support under Grant No. R01CA101644 awarded by the National Cancer Institute. The Government has certain rights in the invention.
| Number | Date | Country | |
|---|---|---|---|
| 61793086 | Mar 2013 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/US2014/026351 | Mar 2014 | US |
| Child | 14853568 | US |
