Patent Application
20090017103
The present invention relates to antisense oligonucleotides targeted to the gene encoding osteopontin (OPN), bone sialoprotein II (BSP II) and/or osteonectin (ON), wherein said oligonucleotides inhibit the expression of said gene(s). The present invention also relates to the therapeutic use of said antisense oligonucleotides, e.g., for the treatment or prevention of bone cancer or metastasis of several types of cancer, preferably osteolytic metastasis or metastasis of breast cancer cells.
Cancer is a life threatening disease not as a result of the primary tumor which can be removed surgically in the vast majority of cases but from its metastatic spread to adjacent and distal sites in the body. Currently used diagnostic techniques do not accurately reflect progression or metastatic spread of a cancer, but recently some evidence has accumulated with respect to markers which are related to the development of progression and metastasis. One molecule of this promising group of markers is the secreted adhesive glycophosphoprotein OPN. This molecule has recently been recognized as a lead marker of human colon cancer progression as shown by a significant correlation between osteopontin protein expression and advanced tumor stage [1]. Similarly, OPN was found to be a metastasis associated protein in human breast cancer in that over-expression of OPN in breast tumors as well as in blood of patients was highly correlated with tumor progression [2,3]. OPN was initially described as a protein the secretion of which was elevated in many transformed cells in culture. Besides this fact it was also identified as a major noncollagenous protein in bone. Moreover, it is a calcium-binding protein that is important in bacterial resistance and immune activity as well as in cell adhesion, signaling, migration and survival of various cells, in addition to being a potent regulator of osseous and ectopic calcification. OPN and bone sialoprotein BSP II are members of the SIBLING (small integrin-binding ligand, N-linked glycoprotein) family of genetically related proteins that are clustered on the long arm of human chromosome 4[4]. These proteins often function by bridging two proteins of fixed structures into a biologically active complex. The structural similarity of BSP II with OPN is paralleled by the observation that both proteins are expressed by certain tumor cells such as breast cancer [5, 6], as well as colon, prostate [7] and lung cancer [8], and have been related to the pathogenesis of bone metastasis [9]. The calcium binding properties of BSP II and its role in initiating and controlling hydroxylapatite crystallization have been related to the formation of micro-calcification in breast cancer. Osteonectin (ON) is a third molecule that has been related to progression of human colorectal [10] and urinary bladder cancer [11] as well as to bone metastasis [12]. It is a non-collagenous, calcium binding glycoprotein which has been mapped to the long arm of chromosome 5 and is related to wound healing and angiogenesis [21]. The current situation is that a successful and specific treatment of cancers/metastasis cannot be achieved.
Therefore, it is the object of the present invention to provide a therapeutic means for the specific treatment/prevention of cancers/metastasis.
According to the invention this is achieved by the subject matters defined in the claims. For a specific treatment, antisense oligonucleotides were identified that are capable of reducing the expression levels of OPN, BSP II and/or ON. The activity of these ASOs was determined by Western Blot and by inhibition of colony formation as well as of metastasis formation of pre-exposed MDA-MB-231GFP human mammary carcinoma cells. This cell line was chosen for its ability to express the three proteins, to form colonies, and to induce lytic bone metastasis in nude rats. The antisense oligonucleotides were effective in reducing protein levels of OPN, BSP II and ON. In human MDA-MB-231 breast cancer cells, the maximum inhibition of protein expression ranged from 84% (OPN) to 75% (BSP II) and 70% (ON). Erucylphospho-NNN-trimethylpropanolamine (ErPC3) was used as positive control and combination partner. Exposure to ErPC3 inhibited colony formation of MDA-MB-231 cells by 11% (10 μM), 45% (14 μM) and 78% (20 μM). The clonogenicity of breast cancer cells was reduced by 15%, 11%, 8% (5 μM), 39%, 19%, 14% (10 μM) and 46%, 39%, 21% (20 μM) in response to ASO-OPN-04, ASO-BSPII-06 and ASO-ON-03, respectively. Combination of ErPC3 with the ASOs caused additive combination effects. Pre-exposure to the ASOs, but not to the NSO, inhibited formation of osteolytic metastasis in 3 of 4 (ASO-OPN-04, p<0.03) and 2 of 4 (ASO-BSPII-06) nude rats, and reduced metastasis lesions significantly (T/C %=4.3 and 9.1, p=0.05, respectively). Thus, it can be concluded that down-regulation of OPN, BSPII and/or ON reduces colony formation of MDA-MB-231 cells and formation of osteolytic metastasis in nude rats and is also effective for inhibiting the formation of metastases in other mammals, e.g., humans. Accordingly, the antisense oligonucleotides of the invention are expected to be useful for therapy or prevention of cancer/metastasis.
(a) 1=urine, 2=MDA MB-231, 3=MDA MB-435s, 4=MDA MB-231 F, 5=MCF-7 6=T47-D, 7=SAOS, 8=urine, 9=HT-29, 10=BV-173, 11=HL-60, 12=K-562 13=ACHN, 14=medium.
The mouse monoclonal antibody against human osteopontin recognizes multiple bands with an apparent size ranging from 60 to 100 kD.
(b) 1=BSP—standard, 2=MDA MB-231, 3=MDA MB-435, 4=MDA MB-231 F, 5=MCF-7, 6=T47-D, 7=SAOS, 8=BSP—standard, 9=HT-29, 10=BV-173, 11=HL-60, 12=K-562, 13=ACHN, 14=medium.
The rabbit polyclonal antibody against human bone sialoprotein II recognizes two bands with an apparent size ranging from 80 to 160 kD. Erythrocytes served as negative control for both, the OPN and BSP II antibodies and, in addition, large bowel mucosa and white blood cells served as negative control for BSP II. Urine was taken from a normal subject and the medium was from MDA-MB-231 cells growing without FBS.
The expression following repeated treatment (a, b) and single treatment (c) is given in percent relative to control treated with lipofectamine. The expression of actin (lower part of a, b, and c) is given for comparison.
showing (a) no osteolysis after injection of MDA-MB-231 cells pre-exposed to ASO-OPN-04, (b) a minute osteolytic lesion in the tibia only after injection of MDA-MB-231 cells preexposed to ASO-BSPII-6 and (c) multiple lesions in the femur, tibia and fibula after injection of control MDA-MB-231 cells.
showing (a) no visible lytic lesions after injection of MDA-MB-231 cells pre-exposed to ASO-OPN-04, (b) a small lesion in the tibia after injection of MDA-MB-231 cells pre-exposed to ASO-BSPII-6 and (c) large osteolytic lesions in the femur, tibia and fibula after injection of MDA-MB-231 cells pre-exposed to NSO.
Start of therapy was immediately after implantation of tumor cells
(a) four weeks after tumor cell implantation: small lytic lesions in the tibia;
(b) six weeks after tumor cell implantation: visible lytic lesions in the tibia;
(c) eight weeks after tumor cell implantation: clear increase of lytic lesions in the tibia, however new formation of bone tissue at the edges of the lesions;
(d) ten weeks after tumor cell implantation: a decrease of the lesions is clearly visible.
Start of therapy was immediately after implantation of tumor cells (for a period of 5 weeks).
(a) four weeks after tumor cell implantation: small lytic lesions in the tibia;
(b) six weeks after tumor cell implantation: visible lytic lesions in the tibia;
(c) eight weeks after tumor cell implantation: clear increase of lytic lesions in the tibia, however new formation of bone tissue at the edges of the lesions (bright areas);
(d) ten weeks after tumor cell implantation: lytic lesions are no longer visible in the region of the tibia.
Start of therapy was immediately after implantation of tumor cells (for a period of 5 weeks).
(a) four weeks after tumor cell implantation: small lytic lesions in the tibia;
(b) six weeks after tumor cell implantation: visible lytic lesions in the tibia and fibula;
(c) eight weeks after tumor cell implantation: clear increase of lytic lesions in the tibia and fibula, in addition, a spontaneous fracture in the neck of the femur can be seen;
(d) ten weeks after tumor cell implantation: lytic metastases with clear deterioration are visible in all regions of the right hind leg.
OPN, osteopontin; BSP II, bone sialoprotein II; ON, osteonectin; ErPC3, Erucylphospho-NNN-trimethylpropanolamine; ASO, antisense oligonucleotide; NSO, nonsense oligonucleotide; SIBLING, small integrin-binding ligand, N-linked glycoprotein; ECM, extracellular matrix; FBS, fetal bovine serum; HUSAR, Heidelberg UNIX sequence Analysis Resource.
Accordingly, the present invention relates to a pharmaceutical composition containing at least one compound 8 to 50 nucleobases in length targeted to (a) nucleic acid molecule(s), preferably mRNA, encoding osteopontin, bone sialoprotein II and/or osteonectin, wherein said compound(s) specifically hybridize(s) with and inhibit(s) the expression of the nucleic acid(s) encoding osteopontin, bone sialoprotein II and/or osteonectin. Preferably, said compound is targeted to mRNA of osteopontin (OPN) and/or bone sialoprotein II (BSP II).
“Targeting” an antisense compound to a particular nucleic acid, in the context of this invention, is a multistep process. The targeting process also includes determination of a site or sites within the gene for the antisense interaction to occur such that the desired effect, i.e., inhibiton of expression of the protein, will result. Within the context of the present invention, a preferred intragenic site is (a) the region encompassing the translation initiation or termination codon of the open reading frame (ORF) of the gene or (b) a region of the mRNA which is a “loop” or “bulge”, i.e., not part of a secondary structure. Once one or more target sites have been identified, oligonucleotides are chosen which are sufficiently complementary to the target, i.e., hybridize sufficiently well and with sufficient specificity, to give the desired 30 effect. In the context of this invention, “hybridization” means hydrogen bonding, which may be Watson-Crick, Hoogsteen or reversed Hoogsteen hydrogen bonding, between complementary nucleoside or nucleotide bases. “Complementary,” as used herein, refers to the capacity for precise pairing between two nucleotides. For example, if a nucleotide at a certain position of an oligonucleotide is capable of hydrogen bonding with a nucleotide at the same position of a DNA or RNA molecule, then the oligonucleotide and the DNA or RNA are considered to be complementary to each other at that position. The oligonucleotide and the DNA or RNA are complementary to each other when a sufficient number of corresponding positions in each molecule are occupied by nucleotides which can hydrogen bond with each other. Thus, “specifically hybridizable” and “complementary” are terms which are used to indicate a sufficient degree of complementarity or precise pairing such that stable and specific binding occurs between the oligonucleotide and the DNA or RNA target. It is understood in the art that the sequence of an antisense compound need not be 100% complementary to that of its target nucleic acid to be specifically hybridizable. An antisense compound is specifically hybridizable when binding of the compound to the target DNA or RNA molecule interferes with the normal function of the target DNA or RNA to cause a loss of utility, and there is a sufficient degree of complementarity to avoid non-specific binding of the antisense compound to non-target sequences under conditions in which specific binding is desired, i.e., in the case of therapeutic treatment.
The skilled person can generate antisense compounds according to the present invention on the basis of the known DNA sequences for OPN, BSP II and ON; see Example 1(C), below. “Oligonucleotide” refers to an oligomer or polymer of ribonucleic acid (RNA) or deoxyribonucleic acid (DNA) or mimetics thereof. This term includes oligonucleotides composed of naturally-occurring nucleobases, sugars and covalent internucleoside (backbone) linkages as well as oligonucleotides having non-naturally-occurring portions which function similarly. Such modified or substituted oligonucleotides are often preferred over native forms because of desirable properties such as, for example, enhanced cellular uptake, enhanced affinity for nucleic acid target and increased stability in the presence of nucleases. While antisense oligonucleotides are a preferred form of the antisense compound, the present invention comprehends other oligomeric antisense compounds, including but not limited to oligonucleotide mimetics such as are described below. The antisense compounds in accordance with this invention comprise from about 8 to about 50 nucleobases (i.e. from about 8 to about 50 linked nucleosides). Particularly preferred antisense compounds are antisense oligonucleotides, even more preferably those comprising from about 15 to about 25 nucleobases. Antisense compounds include ribozymes, external guide sequences (EGS), oligonucleotides (oligozymes), and other short catalytic RNAs and RNAi (siRNA) or catalytic oligonucleotides which hybridize to the target nucleic acid and inhibit its expression.
Alternatively, the pharmaceutical composition of the invention contains a vector allowing to transcribe an antisense oligonucleotide of the invention, e.g., in a mammalian host. Preferably, such a vector is a vector useful for gene therapy. Preferred vectors useful for gene therapy are viral vectors, e.g. adenovirus, herpes virus, vaccinia, or, more preferably, an RNA virus such as a retrovirus. Even more preferably, the retroviral vector is a derivative of a murine or avian retrovirus. Examples of such retroviral vectors which can be used in the present invention are: Moloney murine leukemia virus (MoMuLV), Harvey murine sarcoma virus (HaMuSV), murine mammary tumor virus (MUMTV) and Rous sarcoma virus (RSV). Most preferably, a non-human primate retroviral vector is employed, such as the gibbon ape leukemia virus (GaLV), providing a broader host range compared to murine vectors. Since recombinant retroviruses are defective, assistance is required in order to produce infectious particles. Such assistance can be provided, e.g., by using helper cell lines that contain plasmids encoding all of the structural genes of the retrovirus under the control of regulatory sequences within the LTR. Suitable helper cell lines are well known to those skilled in the art. Said vectors can additionally contain a gene encoding a selectable marker so that the transduced cells can be identified. Moreover, the retroviral vectors can be modified in such a way that they become target specific. This can be achieved, e.g., by inserting a polynucleotide encoding a sugar, a glycolipid, or a protein, preferably an antibody. Those skilled in the art know additional methods for generating target specific vectors. Further suitable vectors and methods for in vitro- or in vivo-gene therapy are described in the literature and are known to the persons skilled in the art; see, e.g., WO 94/29469 or WO 97/00957.
In order to achieve expression only in the target organ, e.g., a tumor to be treated, the DNA sequences for transcription of the antisense oligonucleotides can be linked to a tissue specific promoter and used for gene therapy. Such promoters are well known to those skilled in the art (see e.g. Zimmermann et al., (1994) Neuron 12, 11-24; Vidal et al.; (1990) EMBO J. 9, 833-840; Mayford et al., (1995), Cell 81, 891-904; Pinkert et al., (1987) Genes & Dev. 1, 268-76).
Preferably, an antisense compound of the pharmaceutical composition of the present invention has the nucleic acid sequence (a) 5′-CTA ACT TAA AAA ACA AAA GA-3′ (ASO-OPN-04), 5′-GCT-TTC-TTC-GTT-TTC-ATT-TC-3′ (ASO-BSP II-06), 5′-GGG GGC TGG GCA GCT GGT GG-3′ (ASO-ON-03) or 5′-ATG TTA TAG TTC TTC TCG AA-3′ (ASO-ON-05) or (b) a nucleic acid sequence which has at least 70%, preferably at least 75%, 80%, 85% or 90%, identity with a nucleic acid sequence of (a).
Within an oligonucleotide structure, the phosphate groups are commonly referred to as forming the internucleoside backbone of the oligonucleotide. The normal linkage or backbone of RNA and DNA is a 3′ to 5′ phosphodiester linkage. Specific examples of preferred antisense compounds useful in the present invention include oligonucleotides containing modified backbones or non-natural internucleoside linkages.
Oligonucleotides having modified backbones include those that retain a phosphorus atom in the backbone and those that do not have a phosphorus atom in the backbone. Modified oligonucleotide backbones which can result in increased stability are known to the person skilled in the art, preferably such modification is a phosphorothioate linkage.
A preferred oligonucleotide mimetic is an oligonucleotide mimetic that has been shown to have excellent hybridization properties, and is referred to as a peptide nucleic acid (PNA). In PNA compounds, the sugar-backbone of an oligonucleotide is replaced with an amide containing backbone, in particular an aminoethylglycine backbone. The nucleobases are retained and are bound directly or indirectly to aza nitrogen atoms of the amide portion of the backbone (see, e.g., Nielsen et al., Science, 25, 1991, 254, 1497-1500.)
Modified oligonucleotides may also contain one or more substituted or modified sugar moieties. Preferred oligonucleotides comprise one of the following at the 2′ position: OH; F; 0-, S—, or N-alkyl; 0-, S—, or N-alkenyl; 0-, S- or N-alkynyl; or 0-alkyl-O-alkyl, wherein the alkyl, alkenyl and alkynyl may be substituted or unsubstituted C1 to C10 alkyl or C2 to C10 alkenyl and alkynyl. A particularly preferred modified sugar moiety is a 2′-O-methoxyethyl sugar moiety.
Oligonucleotides of the invention may also include nucleobase modifications or substitutions. Modified nucleobases include other synthetic and natural nucleobases such as 5-methylcytosine (5-me-C), 5-hydroxymethyl cytosine, xanthine, hypoxanthine, 2-aminoadenine, 6-methyl and other alkyl derivatives of adenine and guanine, 2-propyl and other alkyl derivatives of adenine and guanine, 2-thiouracil, 2-thiothymine and 2-thiocytosine etc., with 5-methylcytosine substitutions being preferred since these modifications have been shown to increase nucleic acid duplex stability.
Another modification of the oligonucleotides of the invention involves chemically linking to the oligonucleotide one or more moieties or conjugates which enhance the activity, cellular distribution or cellular uptake of the oligonucleotide. Such moieties include lipid moieties such as a cholesterol moiety, cholic acid, a thioether, a thiocholesterol, an aliphatic chain, e.g., dodecandiol or undecyl residues, a phospholipid, a polyamine or a polyethylene glycol chain, or adamantane acetic acid, a palmityl moiety, or an octadecylamine or hexylamino-carbonyl-oxycholesterol moiety.
The present invention also includes antisense compounds which are chimeric compounds. “Chimeric” antisense compounds or “chimeras,” in the context of this invention, are antisense compounds, particularly oligonucleotides, which contain two or more chemically distinct regions, each made up of at least one monomer unit, i.e., a nucleotide in the case of an oligonucleotide compound. These oligonucleotides typically contain at least one region wherein the oligonucleotide is modified so as to confer upon the oligonucleotide increased resistance to nuclease degradation, increased cellular uptake, and/or increased binding affinity for the target nucleic acid. An additional region of the oligonucleotide may serve as a substrate for enzymes capable of cleaving RNA:DNA or RNA:RNA hybrids. By way of example, RNase H is a cellular endonuclease which cleaves the RNA strand of an RNA:DNA duplex. Activation of RNase H, therefore, results in cleavage of the RNA target, thereby greatly enhancing the efficiency of oligonucleotide inhibition of gene expression. Consequently, comparable results can often be obtained with shorter oligonucleotides when chimeric oligonucleotides are used, compared to phosphorothioate deoxyoligonucleotides hybridizing to the same target region. Chimeric antisense compounds of the invention may be formed as composite structures of two or more oligonucleotides, modified oligonucleotides, oligonucleosides and/or oligonucleotide mimetics as described above. Such compounds have also been referred to in the art as hybrids or gapmers.
The antisense compounds of the invention may be conveniently and routinely made through the well-known technique of solid phase synthesis. Equipment for such synthesis is sold by several vendors. Any other means for such synthesis known in the art may additionally or alternatively be employed. Similar techniques can be used for preparing oligonucleotides such as the phosphorothioates and alkylated derivatives.
In a further preferred embodiment, the pharmaceutical composition of the present invention additionally contains a cytostatic alkylphosphocholine. Suitable alkylphosphocholines are known to the skilled person. A preferred example of a cytostatic alkylphosphocholine is erucylphospho-NNN-trimethylpropanolamine (ErPC3).
Examples of suitable pharmaceutical carriers for the pharmaceutical composition of the present invention are well known in the art and include phosphate buffered saline solutions, water, emulsions, such as oil/water emulsions, various types of wetting agents, sterile solutions etc. Such carriers can be formulated by conventional methods and can be administered to the subject at a suitable dose. Administration of the suitable compositions may be effected by different ways, e.g. by intravenous, intraperetoneal, subcutaneous, intramuscular, topical or intradermal administration. The route of administration, of course, depends on the nature of the disease and the kind of compound contained in the pharmaceutical composition. The dosage regimen will be determined by the attending physician and other clinical factors. As is well known in the medical arts, dosages for any one patient depends on many factors, including the patient's size, body surface area, age, sex, the particular compound to be administered, time and route of administration, the kind and stage of the disease, e.g., tumor, general health and other drugs being administered concurrently.
The delivery of the antisense compounds of the present invention can be achieved by direct application or, preferably, by using a recombinant expression vector such as a chimeric virus containing these compounds or a colloidal dispersion system. Direct application to the target site can be performed, e.g., by ballistic delivery, as a colloidal dispersion system or by catheter to a site in artery. The colloidal dispersion systems which can be used for delivery of the above antisense compounds include macromolecule complexes, nanocapsules, microspheres, beads and lipid-based systems including oil-in-water emulsions (mixed), micelles, liposomes and lipoplexes, The preferred colloidal system is a liposome. Some of these systems (in particular liposomes) provide a slow and/or continuous release of the active compound (antisense compound) which is preferably in some case. Organ-specific or cell-specific liposomes can be used in order to achieve delivery only to the desired tissue. The targeting of liposomes can be carried out by the person skilled in the art by applying commonly known methods. This targeting includes passive targeting (utilizing the natural tendency of the liposomes to distribute to cells of the RES in organs which contain sinusoidal capillaries) or active targeting (for example by coupling the liposome to a specific ligand, e.g., an antibody, a receptor, sugar, glycolipid, protein etc., by well known methods). In the present invention monoclonal antibodies are preferably used to target liposomes to specific tissues, e.g. tumor tissue, via specific cell-surface ligands. The present invention also relates to the use of the compounds of the invention for the preparation of a pharmaceutical composition for the treatment or prevention of bone cancer (primary tumor) or metastasis of several cancer types, preferably for treatment/prevention of metastasis of cancer of the breast, colon, prostate, bone, urinary bladder or colorectal cancer.
The following examples illustrate the invention.
Ten cell lines were used for detecting OPN, BSP II, and ON. They were selected from various organs to establish a possibly differential expression of the three proteins. Therefore, the panel consisted of cancer cells derived from the skeleton (SAOS-2), as well as of cells metastasizing into the skeleton (MDA-MB-231 and MDA-MB-435S). In addition, cells without apparent affinity to the skeleton were used for comparison (K562, HL-60, BV-173, MCF-7, T47D, HT29, and ACHN). The cell lines were obtained from the ATCC or DSZM, respectively, and were grown in media and supplements as recommended by the two organizations (fetal bovine serum, L-glutamine, insulin, Na—HCO3, glucose, hepes, and pyruvate, all from Sigma, Taufkirchen, Germany). For determining the potential secretion of osteopontin and bone sialoprotein, a MDA-MB-231 subline was generated, which was selected by continuously reducing the FBS content of the medium, until the cells kept growing without FBS. This cell line was denoted as MDA-MB-231F. All cells were kept in log-phase, and passaged 1-3 times per week depending of their growth rate, and maintained under standard conditions (37° C., humidified atmosphere, 5% CO2).
For determining the response of MDA-MB-231 colony formation to exposure with antisense oligonucleotides and erucylphospho-NNN-trimethylpropanolamine (ErPC3) the following procedure was used. MDA-MB-231 cells were treated for various periods of time (see below), harvested and counted. Cells (5000) were then transferred into semi-solid medium containing 0.8t RPMI-methylcellulose and 30% FBS. Cells were plated onto 3.5 cm Petri-dishes (1 ml/dish) (NUNC, Wiesbaden, Germany) and usual cell culture conditions (37° C., 5% CO2 in humidified air) were applied. Colony formation (clusters of 30 or more cells) was visualized by staining with 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium-bromide (MTT; Serva, Heidelberg, Germany) and the resulting dark blue colonies were scored by an inverted microscope after 5-7 days. At least three dishes per treatment protocol were used.
The suitability of ten different antisense oligonucleotides (ASOs) per gene was predicted by using the HUSAR program ‘Mfold’ [13,14,15], which takes RNA folding into account. Application of this program onto the cDNA sequence of osteopontin (acc. no. gi:3360431), bone sialoprotein II (acc. no. gi:11435526) and osteonectin (acc. no. gi:14124969) resulted in the recognition of RNA stretches that probably contain bulges or loops, i.e. that are preferentially single stranded and thus allow access of DNA antisense structures. ASOs of 20 base pair lengths were selected against these single stranded regions and synthesized with a phosphorothioate backbone, to increase stability against degrading enzymes (Table 1).
The following sequence from HBV was used as a nonsense control:
1) The combination of the abbreviation of the gene and the number of a given antisense oligonucleotide (ASO) was used for its naming.
Controls included a nonsense oligonucleotide (NSO) derived from HBV genome which served as backbone analog to control for unspecific effects of a 20 bp long phosphorothioate oligomer. In addition its base composition differed only slightly from the mean composition of all ASOs used (A: 3 vs. 4.1; C: 4 vs. 4.4; G: 6 vs. 4.8; T: 7 vs. 6.6). Sequence specific effects were controlled by using ASOs differing by three base pairs with regard to the respective cDNA sequence. Finally, the use of ten ASOs per target gene allowed to include sequences that were scrambled (identical in base composition) except for two bases that were permutated.
Stock solutions of ASOs in distilled water were diluted to appropriate concentrations with phosphate buffered saline. For transfecting cells with ASOs, lipofectamine (Lipofectin, Invitrogen, Karlsruhe, Germany) or electroporation was used.
Pending on the duration of treatment, 5×105-3×106 cells were suspended in one ml RPMI 1640 medium without phenol red containing 10 μM concentrations of the respective ASO or NSO. For transfection, the cells were pulsed two or three times for 2 ms at 450 or 350V, respectively, in a 800 μl cuvette [Eppendorf, Hamburg, Germany] using an electroporation impulse generator (EPI2500, Dr. L. Fischer, Heidelberg, Germany) with the capacitance set at 1200 AF. Thereafter the cells were plated onto 6 wells plates and grown for 48-72 h.
Pending on the duration of treatment, 1×105-3×105 cells were transferred onto 6 well plates (Nunc, Wiesbaden, Germany) and grown for 24 h. For transfection, ASO stock solutions were prepared in medium without FBS. According to the protocol of the manufacturer, the respective ASO stock solution was mixed with lipofectamine to allow ASO-liposome complexes to form. To 200 μl medium containing ASO quantities resulting in 10 μM (Western blot and in vivo model) and in 5, 10, or 20 μM (clonogenicity assay) final ASO-concentrations, an equal volume of medium without FBS was added containing 5, 10, or 20 μl lipofectamine, respectively. In addition to the ASO treatment, a NSO control (20 μM final concentration with 20 μl lipofectamine) and a lipofectamine control (20 μl) were used. Based on the equilibrium of the ASO-liposome complex formation, the relatively low amount of lipofectamine used resulted in effective ASO concentrations that were at least by a factor of ten lower than those in the medium used for transfection. After 12 h the medium was changed, and cells were further grown for 48-72 h. In the case of a sequential combination treatment this first cycle was repeated with the respective combination partner.
The alkylphosphocholine ErPC3 was synthesized and provided by Prof. H. Eibl (MPI of Biophysical Chemistry, Göttingen, FRG). For treating MDA-MB-231 cells, ErPC3 which was kept as stock solution in ethanol and PBS (10 mM; ratio of diluents 1:1; V:V), was diluted in PBS resulting in final concentrations of 10, 14, and 20 μM. The medium containing ErPC3 was changed after 24 h in all experiments and the cells were further grown for 48-72 h without ErPC3 (for details of sequential exposure see below).
Sequential combination treatment consisted of two or three treatment cycles. The two cycle treatment started either with the ASO and was followed by ErPC3 or was performed with the reverse sequence. The three cycle treatment started either with two cycles of ASO followed by ErPC3 or an initial exposure to ErPC3 was followed by two cycles with an ASO.
Colony counts are presented as mean with corresponding standard deviation. For comparison of incidences between treatment groups the x2 test was used and for comparison of the lesion sizes the Kruskal-Wallis test was applied [16]. P values≦0.05 were considered significant. Predicted theoretical values of combinations were calculated according to the equation: C=a×b/100, where a and b are colony counts in percent of untreated control obtained in response to single agents. For each concentration applied theoretical values were calculated and compared with the real value of the combination. In addition, isobologram and multiple drug effect analysis was examined by a suitable program (CalcuSyn, Biosoft, Ferguson, USA) to study the nature of the interaction observed [17,18]. For this purpose, the dose-effect curve for each drug alone was determined based on the experimental observations using the median-effect principle; the combination index (CI) for each combination was then calculated according to the following equation:
CI=(D)1/(Dx)1+(D)2/(Dx)2+(D1)×(D2)/(Dx)1×(Dx)2
where (D)1 and (D)2 are the doses of drug 1 and drug 2 that have x effect when used in combination and (Dx)1 and (Dx)2 are the doses of drug 1 and drug 2 that have the same x effect when used alone. When CI=1, this equation represents the conservation isobologram and indicates additive effects. CI values less than 1.0 indicate a more than expected additive effect (synergism).
For evaluation of the results of the in vivo model, mean value, standard deviation ad the 95% confidence interval (ci) were determined from all data. If the 95% confidence intervals did not show an overlap the differences were regarded as being significant (P≦0.05). For comparison of incidences between treatment groups the χ2 test was used and for comparison of the lesion sizes the non-parametric Kruskal-Wallis test was applied [16]. P-values below 0.05 were regarded as being significant.
Transfected cells were incubated, harvested and washed in PBS. Thereafter cells were counted (Neubauer chamber) and cell pellets (2×106 cells) were suspended in 200 μl buffer [0.1 M NaCl, 0.01 M Tris. Cl (pH 7.6), 0.001 M EDTA (pH 8.0)] containing 1 mM PMSF (Sigma), 50 μg/ml aprotinin (Sigma), 1 mM Na3 VO4, and 2 mg/ml leupeptin (Sigma). After that the cells were lysed by adding 200 μl of lysis buffer [100 mM Tris. Cl (pH 6.8), 200 mM dithiothreitol (Serva, Heidelberg, Germany), 4% SDS, 0.2% bromophenol blue and 20% glycerol]. After vigorously vortexing, lysates were boiled for 10 minutes in a water bath at 100° C. and centrifuged at 14000 rpm for 10 min. at room temperature. The protein concentration of the lysate was determined using the BCA protein assay from Pierce (Rockford, Ill., USA) according to the manufacturer's recommendation. Cell lysates corresponding to 150,000 cells were loaded onto a 6% SDS polyacrylamide gel, separated by electrophoresis and transferred to a PVDF membrane, blocked with 5% skimmed milk in PBS and incubated with the respective first antibody (OPN: rabbit-antihuman polyclonal or mouse-antihuman monoclonal antibody; ON: rabbit-antihuman polyclonal; BSP II chicken-antihuman or rabbit-antihuman polyclonal [all from Immundiagnostik, Bensheim, Germany]) for 2 h in PBS; containing 0.5% milk and 0.5% Triton X-100. After washing with PBS, containing 0.05% Tween 20, an HRP-conjugated anti-mouse, anti-rabbit or anti-chicken secondary antibody (all from Immundiagnostik, Bensheim, Germany) and ECL (Amersham Biosciences, Freiburg, Germany) were used to detect the respective proteins by exposing the membrane to an X ray film (Kodak Biomax, Rochester, N.Y.). To control for variations in loading, the membranes were stripped for 30 min. at 56° C. in stripping solution (62.5 mM Tris HCl, (pH 6.8); 2% SDS; 0.007% β-mercaptoethanol). Thereafter they were reprobed with an antibody against 3-actin (mouse monoclonal antibody, Santa Cruz Biotechnology, Santa Cruz, Calif., USA), and a secondary goat anti mouse polyclonal antibody (Santa Cruz Biotechnology).
The X-ray films were processed by an automatic developing machine (Curix 60, Agfa, Köln, Germany) and the resulting images were scanned by using a digital imaging Program (Adobe photoshop 6.0, Adobe Systems Incorporated). Digitized bands of the respective proteins were given as percent of control and corrected for differences in loading by referring to the intensity of the β-actin band.
Nude rats (RNU strain) were obtained from Harlan (Harlan comp, Borchen, Germany) at an age of 6 to 8 weeks. They were housed under specific pathogen free conditions in a mini-barrier system of the central animal facility. Autoclaved feed and water was given ad libidum to the animals which were maintained under controlled conditions (21±2° C. room temperature, 60% humidity, 12 h light dark rhythm).
The model is based on the human mammary carcinoma cell line MDA-MB-231 which had been marked with GFP. In order to induce loco-regional bone metastasis, and to investigate a preventive effect of the ASOs, 105 MDA-MB-231 cells (control or pre-exposed to ASOs) were injected into a secondary muscular branch of the femoral artery of nude rats. Due to a genetic defect, these rats can not produce T lymphocytes and, thus, show reduced immunocompetence and tolerate human cells. The nude rats (strain: RNU) were obtained from Harlan (Harlan comp, Borchen, Germany) and Charles River (Charles river Deutschland GmbH, Sulzfeld, Germany). The animals were kept in “mini barrier”-systems under SPF conditions. Food (Altromin pellets) and sterilized water were given ad lib. After an average of 28 days following the injection of control cells, lytic metastases could be detected by X-rays (anterior-, posterior, and posterior-anterior). Then, for monitoring the progression of lytic lesions the animals were examined by X-rays once per 1-2 weeks. The sizes of these lesions, which exclusively occurred in the femur, tibia and fibula of the animals, were recorded for up to 10 weeks. Initial experiments with female and male rats using various amounts of MDA-MB-231GFP cells demonstrated that the MDA-MB-231GFP cells induce lytic lesions, preferably in male rats. As could be documented by the X-ray examinations of the initial experiments, after injection of 1×105 untreated MDA-MB-23GFP cells within a period of about four weeks lytic bone metastases form in at least one bone of the hind leg of the rat (tibia, fibula or femur).
Due to the various kinds of application of the ASOs three groups of in vivo experiments were established.
In order to investigate whether the reduced expression of OPN and BSPII achieved by application of specific antisense oligonucleotides is capable of reducing the metastatic potential of the MDA-MB-231GFP cells, the cells were pretreated in vitro with ASOs directed against OPN and BSPII, respectively, (10 μM) which had been previously characterized as promising candidates for three to four days prior to the application to the rats. 15 animals were used that were treated as shown in Table 8. 5 animals were treated with ASO-OPN-4, 5 animals with ASO-BSPII-6, 2 animals with NSO and 2 animals were untreated controls.
(2) In Vivo Treatment with Mini-Osmotic Pumps
The antisense oligonucleotides ASO-OPN-4 and ASO-BSPII-6 which had been previously characterized as being optimal as well as the NSO were applied by use of mini-osmotic pumps (Alzet mini-osmotic pump, Palo Alto, Calif., USA). For that, two pumps filled with 20 mg ASO were subcutaneously implanted in succession. The period of pumping was adjusted to 14 days resulting in a daily dose of 7 mg/kg which was maintained over a period of four weeks. Altogether 13 animals were treated; each of 5 animals were treated with ASO-OPN-4 and ASO-BSPII-6, respectively, and three further animals were treated with the NSO (Table 9).
(3) In Vivo Treatment with ASOs Embedded in Nano-Particles
The ASOs ASO-OPN-4 and ASO-BSPII-6 as well as the NSO were embedded in nano-particles. The particles were suspended in PBS to the intended concentration. Immediately after injection of the MDA-MB-23 GFP cells half of the dose of the suspension of the nano-particles containing the ASOs was injected into the same blood vessel. Four (of the 14 operated animals) were treated with NP-ASO-OPN-4 and each of five animals with NP-ASO-BSPII-6 and NP-NSO, respectively (Table 10).
The expression of OPN and BSP II in a panel of eleven cell lines is shown in
The BSP II antibody recognized two main bands with an apparent molecular weight of 80 kD or higher. Grouping by expression level allowed differentiation between low (MDA-MB-231F), intermediate (K-562), and high levels (all other cell lines). The ON antibody used at first recognized a protein of about 33 kD size. A subsequent antibody, used for experiments as shown in
The Western blot results of protein expression after exposing mammary carcinoma cells to antisense oligonucleotides directed against OPN, BSPII, and ON-mRNA are shown in Table 2 and
252)3)
342)3)
192)
393)
1)The number refers to the corresponding number in table 1, ASO refers to an antisense oligonucleotide directed against osteopontin, bone sialoprotein II, and osteonectin. For concentration used see Example 1.
2)X-ray films documenting chemoluminescence bands were scanned, or digitized bands of the respective protein were expressed in relation to untreated control (100%).
3)mean value
F)MDA-MB231 cells growing without FBS
L)Transfection with lipofectamine
E)Transfection with electroporation
Systematic comparisons showed that ASO-OPN-04, ASO-BSPII-06, and ASO-ON-03 and 05 were the most effective structures within the respective series. Single exposure of cells was enough to reduce the osteopontin expression by 84% in response to ASO-OPN-04. This effect was not increased by repeating the ASO exposure but the protein concentration was kept at a comparable level (77%). A similar efficacy was obtained for ASO-BSPII-06, which caused a by 84% reduced bone sialoprotein expression following single exposure and a by 81% reduced protein level following twofold exposure. Interestingly, MDA-MB-231 cells growing without FBS were less sensitive to ASO exposure, but MDA-MB-435s cells were at least as sensitive as MDA-MB-231 cells.
ASO-ON-03 and 05 were similarly active in reducing osteonectin in MDA-MB-231 cells as shown by decreases of 75% and 70%, respectively. Again, MDA-MB-435s cells were as sensitive as MDA-MB231 cells, but MDA-MB231 cells growing without FBS were more sensitive to ASO exposure.
The inhibition of MDA-MB-231 colony formation is shown in Tables 3-6. Single exposure to the ASOs considered optimal is shown in Table 3.
1)concentration in medium during exposure of cells; for details see Example 1.
2)See table 1 for identification
3)Erucylphospho-NNN-trimethylpropanolamine
4)nonsense oligonucleotide
5)P = 0.05 according to the Kruskal-Wallis test versus all treated groups, except ON, 5 μM
6)P = 0.05 according to the Kruskal-Wallis test versus 10 and 20 μM
7)P = 0.05 according to the Kruskal-Wallis test versus 20 μM
8)P = 0.05 according to the Kruskal-Wallis test versus 14 and 20 μM
9)P = 0.05 according to the Kruskal-Wallis test versus all treated groups of experiment II, except NSO
In contrast to ErPC3 which was used as a standard, effecting 11% (lowest concentration) to 78% (highest concentration, P=0.05, respectively) colony growth inhibition, the ASOs were less effective. Nevertheless, all ASOs reduced the colony growth concentration dependently, and this effect was significantly different from untreated control (P=0.05) except for ASO-ON-03 at 5 μM. ASO-OPN-04 caused 47% colony growth inhibition at the maximum concentration of 20 μM, ASO-BSPII-6 (39%), and ASO-ON-3 (27%) were even less effective at equimolar highest concentrations (20 μM). Serial combined exposure (Table 4) to ASO-OPN-04 (first agent) and ErPC3 (second agent) resulted in colony growth inhibition compared to untreated control ranging from 33% (5 μM ASO OPN-4+10 μM ErPC3) to 93% (20 μM ASO-OPN-4+20 μM ErPC3). Similarly, combination of ASO-BSPII-06 with ErPC3 caused reduction in clonogenic growth ranging from 28% (5 μM ASO-BSPII-06+10 μM ErPC3) to 87% (20 μM ASO-BSPII-06+20 μM ErPC3). Finally, combination of the ASO-ON-03 with ErPC3 caused colony growth inhibition ranging from 14% (5 μM ASO-ON-03+10 μM ErPC3) to 84% (20 μM ASO-ON-03+20 μM ErPC3).
1)concentration in medium during exposure of cells; for details see Example 1.
2)See table 1 for identification
3)Erucylphospho-NNN-trimethylpropanolamine
4)P = 0.05 according to the Kruskal-Wallis test versus all treated groups
5)P = 0.05 according to the Kruskal-Wallis test versus 10 and 20 μM ASO
6)P = 0.05 according to the Kruskal-Wallis test versus 20 μM ASO
Repeated exposure to ASO-OPN-04 (Tab. 5) was more effective than single exposure to this agent, as shown by colony number reduction. Twofold exposure to ASO-OPN-04 at 5 μM reduced colony counts by 16%, and by 60% at 20 μM. Interestingly, repeated exposure to ASO-BSP II-06 caused no increased inhibition of colony formation as compared with single exposure. The combination of this treatment schedule plus a final exposure to ErPC3 (14 μM) caused an additive effect, as shown by 76% to 83% (ASO-OPN-04) and 61% to 75% (ASO-BSPII-06) reduced colony numbers, respectively (Table 5).
1)concentration in medium during exposure of cells; for details see Example 1.
2)control with lipofectamine
3)See table 1 for identification
4)P = 0.05 versus all groups except NSO and lipofectamine.
5)P = 0.05 versus all combinations with ErPC3.
6)P = 0.05 versus ErPC3 (2 × 10; 2 × 20 μM)
7)P = 0.05 versus ErPC3 (2 × 20 μM)
8)P = 0.05 versus the respective combination with ErPC3.
9)P = 0.05 versus 2x OPN (20 μM) + ErPC3 (14 μM).
10)P = 0.05 versus 2x BSP II (10 μM) + ErPC3 (14 μM) and 2x BSP II (20 μM) + ErPC3 (14 μM).
In a subsequent experiment the sequence of agents was reversed (Table 6). Within normal experimental variation, ErPC3 followed by twofold exposure to ASO-OPN-04 or ASO-BSPII-06 was as effective as the reverse sequence in the preceding experiment and all combinations caused significant colony growth inhibition as compared with the respective control.
1)concentration in medium during exposure of cells; for details see Example 1.
2)control with lipofectamine
3)See table 1 for identification
4)P = 0.05 versus all groups except NSO and lipofectamine.
5)P = 0.05 versus all combinations with ErPC3
6)P = 0.05 versus 2 × 10 and 2 × 20 μM.
7)P = 0.05 versus 2 × 20 μM.
8)P = 0.05 versus all combinations with ErPC3
9)P = 0.05 versus 2x OPN (20 μM) + ErPC3 (14 μM).
10)P = 0.05 versus 2x BSP II (10 μM) + ErPC3 (14 μM).
Isobologram analysis of all combinations yielded values not significantly different from 1, thus indicating linear additivity of the combination effects.
The results of the bioassay are shown in Table 7. Exposure to the ASO-OPN-04 and ASO-BSPII-06 for three days before implantation into nude rats caused a significantly reduced tumor take rate, as assessed by the appearance of osteolytic lesions following exposure to ASO-OPN-04, and a reduced size of osteolytic lesions in the X-ray positive rats following both agents.
Nude rats that received 1×105 untreated or NSO-treated MDA-MB-231 breast cancer cells developed bone metastasis in four of four cases (Table 7; c.f.
1/44)
1)Prior to implantation into naked rats GFP-MDA-MB-231 cells were treated with ASO and NSO, respectively (see Example 1 for details)
2)Product of number of pixels × mean value of intensity of blackening of a bone metastatsis per animal of a radiograph (relative unit, R.U.)
3)Ratio of mean lesion sizes of treated rats to control rats × 100
4)P = 0.0028 versus control groups 3 and 4 (χ2-test)
5)P = 0.05 versus control groups 3 and 4 (Kruskal-Wallis test).
6)Numbers in brackets denote standard deviation (SD)
7)Numbers in brackets denote range
For OPN, the ASOs directed against the start codon (ASO-OPN-01) and a loop after the stop codon (ASO-OPN-04) were most effective in down regulating the protein. The fact that an ASO directed towards a sequence after the stop codon is active in suppressing the expression of OPN hints to an activity against pre-mRNA or a triplex formation with DNA and that sufficient concentrations are obtained in the nucleus. The comparison of two overlapping ASOs directed against four target structures, respectively, shows no significant differences between the almost identical ASOs, except for ASO-OPN-04 and ASO-OPN-05. The superiority of ASO-OPN-04 over ASO-OPN-05 might be explained by the increased accessibility of the respective target structures: whereas ASO-OPN-04 can hybridize with 17 nucleotides (85% of total ASO length) to an accessible target site, ASO-OPN-05 can do so only with 14 nucleotides (70% of total ASO-length).
For BSP II, the ASO-pair directed against the region of the start codon (ASO-BSP II-01 and ASO-BSP II-02) was less effective than those directed against the largest loop of the molecule (ASO-BSP II-05 and ASO-BSP II-06). From these two, ASO-BSP II-06 was more effective, in line with its hybridization to a closely neighboring loop. Also, the ASO pair directed to the region of the stop codon was more effective than the average with ASO-10 being slightly superior to ASO-BSPII-09, presumably because ASO-10 can hybridize to the loop as well as a pair of unpaired nucleotides.
For ON, the ASO directed against the start codon (ASO-ON-1) was of average activity, as well as those directed to sites after the stop codon (ASO-ON-08-ASO-ON-10). The highest activity was associated with two ASOs (ASO-ON-03 and ASO-ON-05) spanning over a small series of bulges. However, no ASO was really outstanding over all other structures.
With regard to the transfection method used, differences resulting in the resulting protein level were observed in this study, e.g. for ASO-BSP II-05 and -07 when using lipofectamine and electrotransfection (Table 2). Overall, however, the effects were comparable, although the effective ASO concentrations were at least tenfold lower when using lipofectamine.
When comparing the most effective ASOs, as assessed from Western blot, for their activity to reduce colony formation of MDA-MB-231 cells, the efficacy decreased at equimolar levels from OPN (ASO-OPN-04) to BSP II (ASO-BSP II-06) and ON (ASO-ON-03). This difference could result either from differential suppression of the respective protein levels (ASO-OPN-04: 85%; ASO-BSP II-06: 75%; ASO-ON-03: 75%) or from a differential importance of the target proteins supporting colony growth. Colony formation reflects the ability of a specialized compartment of tumor cells to grow anchorage independently and to reproduce themselves in the absence of neighboring cells. Therefore, inhibition of colony formation is indicative of an inhibition of autocrine stimulation. It is noteworthy, that reduced levels of all three proteins investigated were associated with inhibition of colony formation, indicating that OPN, BSPII, and ON acted as direct or indirect mitogens. Since the treatment effect of the ASOs are clearly reversible, as shown by increased protein expression levels after five days and gain of migrating functions, the effects seen after 5-7 days (clonogenicity) and 28 days (in vivo) are related to an early inefficiency of the cells to form colonies, to migrate, or to seed into the bone compartment. The extent of response to the ASOs, which was additively increased by repeated exposure, was clearly dependent on the respective concentrations used. In combination with ErPC3 all ASOs showed additive activity, as can be derived from their combination index, respectively, that varied around 1. This is in line with the assumption that both combination partners act on different targets.
Furthermore, the result show that exposure to an ASO directed against OPN was instrumental in inhibiting the formation of osteolytic lesions in three of four animals used, and in reducing the lesion size of the remaining rat. A similar effect in response to down modulating BSP II-levels has not been described so far. Although slightly less active, the reduction of BSP II levels caused an effect which parallels that of reducing OPN levels. These results suggest that reduction of OPN and BSP II levels in vivo could be instrumental for a combination treatment of cancer, specifically of osteolytic metastasis. In conclusion, suited ASOs reduced the respective protein levels of OPN, BSPII, and ON specifically. Their activities in inhibiting colony growth and formation of osteolytic bone metastasis suggest a beneficial effect in restraining the growth of metastasis in vivo, as well.
In this experiment cells were used that had been treated with antisense oligonucleotides prior to tumor implantation. Altogether, 12 animals were used (Table 7), four animals per group. The animals of the control group received NSO (two rats) and untreated cells (two rats).
Pretreatment of the MDA-MB-231GFP with ASOs directed against OPN and BSPII-6, respectively, inhibited the formation of lytic bone lesions. Pretreatment with ASO-OPN-4 was slightly more effective than pretreatment with ASO-BSPII-6 (
The results of this therapy group are in detail described in Table 8. After four weeks, three out of five animals that were treated with ASO-OPN-4 by use of mini-osmotic pumps developed lytic metastases having sizes of 20 to 41 relative units (R.U.), the other two animals did not show any signs indicative of lytic metastases. One out of the two animals did not develop visible metastases during the entire observation period, the other animal showed visible lytic metastases only after week 8. One out of the four animals showing metastases died after 10 weeks and showed a large lesion (sizes of metastases: 435 R.U.). The remaining three animals exhibited a continuous decrease of metastases after week 8 and 9, respectively. This decrease is clearly visible compared to the NSO control (58% to 26% T/C as determined at weeks 4 to 12; see Table 8 und
Therapy with ASO-BSPII-6 seemed to be more efficient compared to the ASO-OPN-4 group (on average 13 R.U. at week 4 to 9 RE at week 12). Only one animal out of the five animals treated did not develop metastases, however even after six weeks the lytic metastases of a further animal completely receded.
During the remaining observation period metastases were also absent in this animal (Table 8).
1)The corresponding ASOs were applied to the animals by use of mini-osmotic pumps which were dorsal-subcutaneously implanted.
2)Product of number of pixels × mean value of intensity of blackening of a bone metastasis per animal of a radiograph (relative unit, R.U.).
3)Ratio of mean lesion sizes of treated rats to control rats × 100.
4)The numbers in brackets indicate the standard deviation (SD).
A third animal also responded very well to the ASO-BSPII-6 therapy: At the end of the observation period of 12 weeks the animal did not show any metastases and was regarded as being cured according to the radiograph (
The remaining two animals also showed a clear drop of metastasis compared to the NSO group. In summary, the efficiency of therapy with ASO-BSPII-6 (compared to the NSO group) was more definite compared to the ASO-OPN-4 group (T/C=39% in week 4 and 2% in week 12). It has to be emphasized that all animals of the control group developed lytic metastases which continuously proliferated during the observation period (
The results of this therapy group are in detail described in Table 9. Two out of the four animals that were treated with nano-particles containing ASO-OPN-4 did not show any visible metastases during the entire observation period. In one out of the remaining two animals metastases receded and after week 10 no longer any lesions were detectable. The lytic lesions of the third animal which initially increased receded from week 8 until they almost got their initial sizes. All in all, the average values of the sizes of metastases of this group were 7 R.U. at week 4 to 4.5 R.U. at week 12 (T/C=43.7% to 5.3% in the same period). Two out of the five animals that were treated with nano-particles containing ASO-BSPII-6 did not show any visible metastases during the entire observation period. A third animal of this group did no longer show any signs of visible metastases after week 10. The remaining two animals showed—as the OPN group—an involution of metastases at the end of the observation period (T/C=35.7% to 14% from week 8 to 12). All in all, the decrease of the lytic lesions of this group was very clear compared to the control group which was treated with nano-particles containing NSO (T/C=56.3% at week 4 to 14% at week 12).
One out the five animals of the control group which had been treated with nano-particles containing NSO did not develop any visible lytic metastases during the entire observation period. A further animal (out of the remaining four animals) showed a decrease of the visible lesions after week 8. The remaining three animals showed an increase of the lytic metastases during the entire course of the observation period. The sizes of the lesions quintupled from week 4 to week 12 (from 16 R.U at week 4 to 85 R.U. at week 12).
1)The animals were treated with ASOs or NSO embedded into nanoparticles
2)Product of number of pixels × mean value of intensity of blackening of a bone metastasis per animal of a radiograph (relative unit, R.U.).
3)Ratio of mean lesion sizes of treated rats to control rats × 100.
The results of the experiments described above suggest that reduction of the expression of OPN and/or BSPII in vivo is useful for a combination therapy of bone metastases. It can be concluded that suitable ASOs are capable of specifically reducing the expression of OPN and BSPII resulting not only in a reduction of proliferation, colony formation and migration of metastasizing tumor cells in vitro, but also in a significant inhibition of formation of metastases in vivo.
| Number | Date | Country | Kind |
|---|---|---|---|
| 03 020 789.8 | Sep 2003 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP2004/009738 | 9/1/2004 | WO | 00 | 1/31/2007 |
