Patent Application
20080015160
The present invention relates to a method of detecting canceration and malignancy of cancer using a specific cancer-associated gene as an index, and also relates to a method of suppressing/treating cancer using a specific cancer-associated gene as essential part.
A mortality rate of cancer is presently the top end in Japan and occupies one third of the total mortality causes. The mortality rate of cancer goes on increasing and is predicted to occupy about 50% in 10 years. It has been elucidated that cancer is caused and aggravated due to accumulation of abnormalities of many genes. It has been reported that acceleration of oncogene expression and deceleration of cancer suppressor gene expression due to deletion are involved in canceration. Furthermore, it is also known that abnormalities of a gene directly involved in cell differentiation and proliferation and a gene involved in a DNA repair system are involved in canceration.
However, studies that have been hitherto conducted are not sufficient to explain the canceration mechanism in cancer patients. A group of genes involved in canceration varies depending upon the type of cancer. Furthermore, since the individual characters of cancers differ even if they belong to the same type, it has been difficult to systematically analyze the abnormality of which gene group causes cancer. Therefore, it cannot be said that a sufficient diagnostic method for the initial state of cancer and a sufficient diagnostic means for checking degree of malignancy of cancer based on genomic analysis of cancer cells have been provided.
An object of the invention is to find a cancer-associated gene to be used as an index for detecting canceration of cells and degree of malignancy of cancer and to provide a method for detecting cancer using the cancer-associated gene as an index. Another object of the present invention is to provide a method of suppressing/treating cancer using the cancer-associated gene as essential part.
Generally, when a chromosomal abnormality takes place, the cell causes apoptosis to death. Therefore, proliferation of an abnormal cell does not occur in mechanism. However, in some cases, a cell having a chromosomal abnormality may happen to initiate proliferation for an unknown reason through a loophole of the biological control mechanism that should be strictly controlled, thus initiating canceration. Therefore, amplification and deletion of a genome at a chromosomal level are critical causes of canceration. In the case of amplification, expression of a gene present in the amplified genomic region is accelerated, whereas, in the case of deletion, the expression level of a gene present in the deleted genomic region is significantly decelerated. When such abnormalities are accumulated, a cell may probably cause unregulated proliferation.
Comparative genomic hybridization (CGH) is a simple and quick method, that is, the best method, for analyzing gene abnormalities associated with genomic amplification and deletion of a plurality of genes. To analyze abnormality of a gene on the genome involved in canceration and malignant alteration of cancer, it is extremely important to select a group of genes to be printed on a CGH microarray.
The present inventors screened a group of highly potential genes that may be involved in canceration from the databases “National Cancer for Biotechnology” and “University of California Santa Cruz Biotechnology.” They further subjected the DNA thus screened to BLAST search to select genes that conceivably play an important role in the onset of cancer. BAC/PAC clones containing these candidate cancer-associated genes are carefully selected and individually amplified (inexhaustibly amplified). Then, about 800 types of clones thus amplified were loaded on a substrate to form a “MCG cancer array” substrate (hereinafter also referred to “MCG cancer array”). The present invention encompasses the MCG cancer array within its technical range.
The present inventors found cancer-associated genes to be used as cancer detection indexes in several types of cancer by use of the MCG cancer array. Based on the finding, they accomplished one of the present inventions.
More specifically, the present invention provides a method of detecting (hereinafter referred to also as “the detection method of the invention”) cancer using a specific cancer-associated gene as an index. Also in the present invention, there is provided a means for suppressing/treating cancer using the cancer-associated gene. More specifically, the present invention provides a means for suppressing/treating cancer by introducing a specific deletion cancer-associated gene into a cancer cell and a means for suppressing/treating cancer by inhibiting the finction of the transcriptional product (mRNA) of a specific amplification cancer-associated gene. These means for suppressing/treating cancer will be explained later.
The present invention provides a method for detecting pancreatic carcinoma, wherein canceration of a specimen is detected based on an index of not less than 1.5 fold amplification of at least one gene selected from the group consisting of KRAG gene, PTPN1 gene, KRAS2 gene, PTHLH gene, BCLX gene, DEK gene, IGFBP1 gene, MYC gene, Livin-2 gene, PVT1 gene, PRex1 gene, BCAS1 gene, TFAP2C gene, EGFR gene, TGIF2 gene, TNFRSF5 gene, TNFRSF6B gene, EIF4G gene, PMS2 gene, HCK gene, MYBL2 gene, ELM02 gene, PCTK1 gene, CDC2L1 gene, CDC10 gene, TCRG gene, GLI3 gene, PPP1A gene, ZNF217 gene, SRC gene, SUPT5H gene, AKT2 gene, TRRAP gene, Smurf1 gene, PDAP1 gene, PVT1 gene, and MIA gene; in the specimen in comparison with a normal cell.
The present invention further provides a method for detecting pancreatic carcinoma according to the present invention as mentioned above, wherein canceration of a specimen is detected based on an index of not less than 4 fold amplification of at least one gene selected from the group consisting of SUPT5H gene, AKT2 gene, TRRAP gene, Smurf1 gene, PDAP1 gene, MYC gene, PVT1 gene, KRAS2 gene, KRAG gene, and MIA gene; in the specimen in comparison with a normal cell.
The present invention further provides a method for detecting pancreatic carcinoma, wherein canceration of a specimen is detected based on an index of a heterozygous deletion of at least one gene selected from the group consisting of MTAP gene, DCC gene, N33 gene, AAC1 gene, GRP gene, TEK gene, D8S504 gene, NAT2 gene, LZTS1 gene, TNFRSF10 B gene, D9S913 gene, GASC1 gene, FVT1 gene, MAP3K7 gene, DLC1 gene, MALT1 gene, stSG42796 gene, BAIAP1 gene, BLK gene, LPL gene, NRG1 gene, MLLT3 gene, MADH2 gene, SCCA1 gene, SCCA2 gene, NKX3A gene, SMAD7 gene, MLL1 gene, PI5 gene, Casp3 gene, SSXT gene, BCL2 gene, JAK2 gene, PTPRG gene, VIM gene, stSG27915 gene, RH68621 gene, CTDP1 gene, SHGC-145820 gene, EEF1E1 gene, ESR1 gene, KLF12 gene gene, CDKN2A (p16) gene, DEC1 gene, CDH23 gene, and SMAD4-2 gene; in the specimen.
The present invention further provides a method for detecting pancreatic carcinoma, wherein canceration of a specimen is detected based on an index of a homozygous deletion of at least one gene selected from the group consisting of CDKN2A (p16) gene, MTAP gene, N33 gene, MLLT3 gene, TEK gene, DEC1 gene, CDH23 gene, and SMAD4-2 gene; in the specimen.
Preferably in the above, the detection is performed by a CGH method, DNA chip method, quantitative PCR method or real time RT-PCR method.
Preferably in the above, detection is performed by a CGH method or DNA chip method and a plurality of types of DNA fragments to be fixed onto the detection substrate are genomic DNA, cDNA or synthetic oligonucleotides.
Preferably in the above, the detection is performed by a CGH method, and a plurality of types of DNA fragments to be fixed onto the detection substrate are genomic DNA, and the genomic DNA is a gene amplification product of BAC DNA, YAC DNA or PAC DNA.
The present invention further provides a method for suppressing a pancreatic carcinoma cell, which comprises introducing a gene, whose deletion is involved in canceration of a pancreatic carcinoma cell, into a pancreatic carcinoma cell.
The present invention further provides a method for suppressing a pancreatic carcinoma, which comprises introducing at least one gene selected from the group consisting of N13 gene, MTAP gene, CDKN2A(p16) gene, TEK gene, MLLT3 gene, DEC-1 gene, CDH23 gene, and SMAD4-2 gene into a pancreatic carcinoma.
The present invention further provides a method of suppressing a pancreatic carcinoma cell, which comprises applying, to a pancreatic carcinoma cell, a nucleic acid antagonizing a transcriptional product of a gene whose amplification is involved in canceration of the pancreatic carcinoma cell.
The present invention further provides a method of suppressing a pancreatic carcinoma cell, which comprises applying, to a pancreatic carcinoma cell, a nucleic acid antagonizing a transcriptional product of at least one gene selected from the group consisting of SUPT5H gene, TRRAP gene, PVT1 gene, KRAS2 gene, KRAG gene, Smurf1 gene, PDAP1 gene, MYC gene and MIA gene.
Preferably, the nucleic acid antagonizing a transcriptional product of a gene is small interference RNA against a transcriptional poroduct mRNA, or an antisense oligonucleotide of the mRNA.
A. The detection method of the invention
The detection according to the invention may be carried out by CGH method, DNA chip method, quantitative PCR method, or real time RT-PCR method. To detect amplification or deletion of a gene, the DNA chip method or CGH method is preferably used and the CGH method is particularly preferable. When the expression of a cancer suppressor gene (corresponding to the “deletion gene” mentioned above) is suppressed by another cause except for gene deletion, such as acceleration of methylation of a CpG island of the gene and deceleration of acetylation of a protein associated with the gene, it is preferable to employ a detection means for detecting an transcriptional product of the gene, such as the real time RT-PCR method and the DNA chip method, capable of quantifying the transcribed product of the gene.
The specimen to be subjected to the detection method of the present invention is derived from a subject and corresponds to the type of cancer to be detected. To explain more specifically, a pancreatic biopsy specimen is used when a subject is checked for pancreatic carcinoma.
As a preferable embodiment of the detection method of the present invention, mention may be made of application of a CGH method to a substrate on which a plurality of types of gene amplification products having a specific genome DNA region obtained from a BAC (bacterial artificial chromosome) DNA, YAC (yeast artificial chromosome) DNA, or PAC (phage artificial chromosome) DNA are individually and separately fixed. In this embodiment, amplification and deletion gene of a genomic DNA can be analyzed by the CGH method.
The amount of the BAC DNA generally obtained is too little to fix onto numerous substrates practically used as genomic DNA fixed substrates. Therefore, the DNA must be obtained as an amplified product of a gene (the amplification process of the gene is also called as “inexhaustible process”). In the inexhaustible process, BAC DNA etc., was digested with a 4-nucleotide recognition enzyme, such as RsaI, DpnI, or HaeIII, and then, an adapter was added to ligate the digested fragments. The adapter is an oligonucleotide formed of 10 to 30 nucleotdes and preferably 15 to 25 nucleotides. The double stranded chain has a complementary sequence. After annealing, the 3′ end of the oligonucleotide forming a smooth end must be phosphorylated. Then, using a primer having the same sequence as one of the oligonucleotides serving as the adaptor, amplification is performed by PCR (Polymerase Chain Reaction). In this manner, the inexhaustible process can be carried out. On the other hand, an aminated oligonucleotide having 50 to 70 nucleotides characteristic in each of the BAC DNA and the like may be used as a detection probe.
The inexhaustibly amplified BAC DNA or the like (the same in the embodiment genomic DNA, cDNA or synthetic oligonucleotide is used) is fixed onto a substrate, preferably a solid substrate, to manufacture a desired DNA fixed substrate.
Examples of the solid substrate include glass, plastic, membrane and a three-dimensional array. Preferably a glass substrate such as a slide glass is preferable. The solid substrate formed of such as glass is preferably coated by depositing poly-L-lysine, amino silane, gold, and aluminium thereon and applied by an amino group modified DNA immobilization surface treatment.
The concentration of the inexhaustibly amplified DNA mentioned above (the same in the embodiment genomic DNA, cDNA or synthetic oligonucleotide is used) to be spotted on the substrate is preferably 10 μg/μl to 5 μg/μl, and more preferably, 1 μg/μl to 200 μg/μl. The amount of the spot is preferably 1 nl to 1 μl, and more preferably, 10 nl to 100 nl. The size and shape of individual spots to be fixed on the substrate are not particularly limited; however, for example, may be a diameter of 0.002 to 0.5 mm and a circular to elliptic shape as viewed from the top. The thickness of dry spots is not particularly limited; however, may be 1 to 100 μm. The number of spots are not particularly limited; however, preferably 10 to 50,000, and more preferably 100 to 5,000. Each DNA may be spotted in the range of a singular spot to quadruplicated spots, and preferably duplicated or triplicated spots.
The dry spots may be prepared by spotting a plurality of spots of BAC DNA and the like (the same in the embodiment genomic DNA, cDNA or synthetic oligonucleotide is used) inexhaustibly amplified on a substrate by means of a spotter, and drying the spots. As the spotter, use may be made of an inkjet printer, pin array printer, and bubble-jet (registered trade mark) printer; however, an inkjet printer may be preferably used. More specifically, use may be made of GENESHOT (NGK insulators Ltd., Nagoya) and high-throughput inkjet delivery system SQ series (manufactured by Cartesian Technologies, USA), etc.
In the manner mentioned above, a desired DNA fixation substrate can be manufactured by fixing BAC DNA and the like (the same in the embodiment genomic DNA, cDNA or synthetic oligonucleotide is used) inexhaustibly amplified on a substrate, and preferably a solid substrate. Hybridization was actually performed using Cy-3 labeled genomic DNA derived from a normal diploid cell, and Cy-5 labeled genomic DNA derived from the same normal diploid cell separately on the MCG cancer array. The results are shown in
In the MCG cancer array shown in
Furthermore, actually, DNA derived from a normal cell was labeled with Cy-5 and DNA derived from a cancer cell was labeled with Cy-3. They were subjected to comparative genomic hybridization. Data were taken in by a GenePix 4000B scanner. Individual pixels were analyzed and the results are shown in
To identify a group of genes present in the chromosomal region amplified and deleted in a cancer cell by use of the MCG cancer array, genomic DNA derived from a healthy person and genomic DNA derived from a lung cancer cell are labeled with mutually different dye, for example, Cy-3 and Cy-5, in accordance with a customary method (for example, a nick translation method using dCTP). The labeling kits using the nick translation method using dCTP are sold by PanVera (Takara Shuzo Co., Ltd., a distributor in Japan) and Invitrogen (CA, USA). When the labeled DNA is hybridized with the DNA printed on the CGH array, it is more preferable to add Cot-1DNA, formamide, dextran sulfate, SSC (150 mM NaCl/15 mM sodium citrate), Yeast t-RNA, and SDS (sodium dodecyl sulfate). Furthermore, it is preferable to add a solution containing labeled DNA after it is denatured with heat. As a container for use in hybridization, a container that can be placed on a platform having a locking finction and can bring a small amount of solution uniformly into contact with the array is preferable, and use of e.g., hybriman, is more preferable. The temperature of hybridization is preferably 30 to 70° C. and more preferably 38 to 45° C. The hybridization time is preferably 12 to 200 hours and more preferably 40 to 80 hours. The array can be washed with formamide, SSC solution or the like at room temperature. The washing of the array is an important step to reduce a nonspecific signal as much as possible. More preferably, the array was washed at room temperature, and then, washed with the same washing solution at 40 to 60° C., further washed in a solution containing SSC-SDS at 50° C., allowed to stand in a solution containing phosphate buffer/NP-40, and finally shaken in a solution containing SSC.
(1) Group of Genes Present in the Chromosome Amplified and Deleted in Pancreatic Carcinoma
Using the MCG cancer array, a group of genes present in the chromosomal region amplified or deleted in a pancreatic carcinoma cell was identified. As a result of checking a gene amplified in the chromosome of a pancreatic carcinoma cell having a Ratio value of 1.32 and or more, KRAG, PTPN1, KRAS2, PTHLH, BCLX, DEK, IGFBP1, MYC, Livin-2, PVT1, PRex1, BCAS1, TFAP2C, EGFR, TGIF2, TNFRSF5, TNFRSF6B, EIF4G, PMS2, HCK, MYBL2, ELMO2, PCTK1, CDC2L1, CDC10, TCRG, GLI3, PPP1A, ZNF217, and SRC genes were detected. As a gene having a Ratio value of 4 or more, that is, a gene amplified 4-fold or more than that of a normal cell gene, SUPT5H, AKT2, TRRAP, Smurf1, PDAP1, MYC, PVT1, KRAS2, KRAG, MIA genes were detected.
On the other hand, a group of genes present in a chromosomal region deleted in a pancreatic carcinoma cell was analyzed. As a result, as a gene having a Ratio value as low as 0.75 or less, that is, determined as a heterozygote, MTAP, DCC, CDKN2A (p16), N33, AAC1, SMAD4-2, GRP, TEK, D8S504, NAT2, LZTS1, TNFRSF10B, D9S913, GASC1, FVT1, MAP3K7, DLC1, MALT1, stSG42796, BAIAP1, BLK, LPL, NRG1, MLLT3, MADH2, SCCA1, SCCA2, NKX3A, SMAD7, MLL1, P15, Casp3, SSXT, BCL2, JAK2, PTPRG, VIM, stSG27915, RH68621, CTDP1, SHGC-145820, EEF1E1, ESR1, and KLF12 genes were detected.
Furthermore, as a gene having a Ratio value of 0.25 or less, that is, having a homozygous deletion, CDKN2A(p16), MTAP, N33, MLLT3, TEK, DECI, CDH23, and SMAD4-2 genes were detected.
By checking amplification and deletion of the chromosomal region of the group of genes thus detected and analyzing the group of genes amplified and deleted, pancreatic carcinoma can be diagnosed.
As described above, the amplification and deletion of the chromosomal region in pancreatic carcinoma are analyzed by use of the MCG cancer array, and thus a group of genes having amplified and deleted can be identified. Based on the results, it is possible to understand the state of each cancer. To describe more specifically, it is possible to determine whether a tumor is benign, intermediate or malignant. In the case of a malignant tumor, it is possible to provide important findings to determine the grade of the cancer. It is further possible to provide data for efficient chemotherapy performed after a cancerous foci is surgically removed.
It is possible and preferable to simultaneously detect deletion of a chromosome and suppression of expression by monitoring the gene expression by a real time RT-PCR method or a DNA chip method in a deletion cancer gene group.
B. Suppression/Treatment Means for a Cancer by a Cancer-Associated Gene
The suppression/treatment means for a cancer provided by the present invention are roughly divided into two groups. One (1) is a method of suppressing the cancer cell (hereinafter referred to as “suppression/treatment means 1”) by introducing a gene whose deletion is associated with canceration of a cell (called as a deletion cancer gene) into a cancer cell. The other (2) is a method of suppressing the cancer cell (hereinafter referred to as “suppression/treatment means 2”) by applying a nucleic acid antagonizing against a transcriptional product of a gene whose amplification is associated with canceration of a cell (called as an amplification cancer gene) to a cancer cell.
(1) Suppression/Treatment Means 1
Of the deletion cancer genes mentioned above, many of the genes in the chromosomal region exhibiting a homozygous deletion are detected to fall within the category of a cancer suppressor gene. Of them, a gene suppressing proliferation of target cancer cells or a gene inducing apoptosis of cancer to death can be introduced into a cancer cell by use of a Sendai virus vector or adenovirus vector. In a gene therapy using these virus vectors, as a promoter for the homozygous deletion gene to be expressed, a promoter highly expressed in a cancer tissue but not highly expressed in a normal tissue, such as human CXCR4 promoter (Zhu Z B, Makhija S K, Lu B, Wang M, Kaliberova L, Liu B, Rivera A A, Nettelbeck D M, Mahasreshti P J, Leath C A, Yamaoto M, Alvarez R D, Curiel D T: Transcriptional targeting of adenoviral vector through the CXCR4 tumor-specific promoter, Gene ther., 11, 645-648, 2004) and Survivin promoter are preferably used. Each of these recombinant viruses can be combined with a ribosome to form a composite, which may be introduced into a cancer tissue. Alternatively, it can be introduced in the form of naked DNA into a cancer tissue.
Using a viral vector and a promoter as mentioned above, each cancer therapy can be made by selecting a gene from following candidate genes: N13 gene localized in 8p22, MTAP gene and CDKN2A(p16) gene localized in 9p21, TEK gene localized in 9p21.2, MLLT3 gene localized in 9p22, DEC-1 gene localized in 9q32, CDH23 gene localized in 10q22.1, and SMAD4-2 gene localized in 18q21 for pancreatic carcinoma;
CDKN2A(p16) gene is a cyclin dependent kinase inhibitor located in a chromosome 9p21 and considered as a cancer suppressor gene. P16 protein, when it binds to CDK4 kinase, is suppressed in its activity, thereby suppressing cell cycle progression. The CDKN2A(p16) gene is deleted in a wide variety of cancers such as acellular esophageal carcinoma, malignant glioma, gastric carcinoma, pancreatic carcinoma and thyroid carcinoma. MTAP is a gene encoding 5′-methylthioadenosinephosphorylase, which is the first enzyme of a methionine salvage pathway and considered as a cancer suppressor gene. The product of the methionine salvage pathway inhibits the activity of ornithine decarboxylase highly expressed in cancer. RIZ is a gene encoding an RB interacting Zinc Finger protein found in leukemia and belongs to Nuclear protein methyltransferase superfamily. DBCCR1 is found as a gene deleted in chromosome 1 of the bladder carcinoma and considered as a cancer suppressor gene. TEK is an angiopoietin-1 receptor, which is otherwise designated as Tie-2. When TEK is phosphorylated by tyrosine kinase, angiogenesis is induced. CDH23 is cadherin related 23 gene, belongs in the cadherin superfamily, and is a glycoprotein associated with calcium dependent cell adhesion. CXADR gene encodes receptors of coxsachie virus and adenovirus. cIAP1 gene encodes an apoptosis inhibitor. FLI1 gene is classified into an ETS transcription factor. TSPY gene is present in human Y chromosome and encodes a testis specific protein. LRP1B is abbreviation of lipoprotein receptor-related protein 1B, which is a cellular membrane receptor using urokinase and a plasminogen activator, etc., as a ligand, and is considered as a cancer suppressor gene. DEC1 refers to “deleted in esophageal cancer 1” and loss of heterozygosity is frequently detected in esophageal carcinoma and squamous cell carcinoma of the bladder, lung and head and neck portion. MMP1 and MMP7 are matrix metalloproteinase and enzymes involved in vascularization. SMAD4 gene is a cancer suppressor gene whose deletion is found in pancreatic carcinoma and encodes a protein that is activated by a receptor and transferred to a nucleus to derive a transcriptional activation activity. ETS1 is a transcription factor and derives angiopoietin-2 gene, etc. RB1 is a retinoblastoma gene and a cancer suppressor gene.
A virus vector is prepared by integrating a gene as mentioned above downstream of a promoter highly expressed in a cancer tissue, and is then introduced into the cancer tissue of a cancer patient. The gene is allowed to express, thereby reducing cancer in size and inhibiting metastasis. In this way, recurrence of cancer after cancer is excised out can be prevented.
(2) Suppression/Therapeutic Means 2
Of the amplification cancer genes found above, a group of genes present in the chromosome, amplified 4-fold or more than that of a normal cell, are shown in Table 1.
When these groups of genes are compared to those of a normal cell, the number of genome copies in chromosomes 1 to 22 increases to 8 or more, and that in X and Y chromosomes increases 4 or more. The transcriptional product of a highly expressed gene is decomposed by adding the small interference RNA corresponding to the transcriptional product (mRNA) in accordance with an RNAI (RNA interference) method. In this manner, cancer can be treated. Design and synthesis of siRNA and the transfection of siRNA to a cell, confirmation of the effect of RNAi can be performed by conventional methods with reference to, for example, Takara Bio RNAi Book, “Experimentation protocol” (published by Takara Bio Inc., Shiga prefecture). Examples of siRNA to be used herein include Hairpin siRNA, which can be expressed by using an siRNA oligonucleotide and a pSilencer vector (manufactured by Funakoshi Co., Ltd., Tokyo).
On the other hand, mRNA of a cancer gene amplified and excessively expressed in a cancer can be knocked out by use of an antisense oligonucleotide. In this case, s-oligonucleotide is preferably used to inhibit amplification of a cancer cell since it has a good intracellular stability compared to a general oligonucleotide. SiRNA, Hairpin siRNA and s-oligonucleotide, which are found to be effective by use of a cancer cell, can be evaluated in a nude mouse having a cancer cell transplanted therein.
In this case, it is preferable to construct a delivery system such that these RNA can be accumulated in a cancer tissue.
Based on the search for genome database website of the National Cancer for Biotechnology and University of California, Santa Cruz Biotechnology as well as BLAST search of DNA screened, BAC/PAC clones having an extremely important gene for canceration and amplification of a cancer cell or having a sequence tagged site marker were selected.
BAC and PAC DNA was digested with DpnI, RsaI, and HaeIII, and thereafter ligated with adaptor DNA. PCR was performed twice using a primer having the sequence of the adaptor. One of the two ends of the primers has the 5′ end aminated. This process is called an inexhaustible process and DNA thus obtained is defined as inexhaustible DNA. The inexhaustible DNA is placed in an ink-jet type spotter (GENESHOT, NGK Insulators, Ltd., Nagoya) and covalently printed, in duplicate, onto an oligo DNA micro array (manufactured by Matsunami Glass, Osaka).
Using the “MCG cancer array,” an amplified and deleted gene was analyzed with respect to pancreatic carcinoma cells. A gene amplified and having a Ratio value of 1.32 or more was checked. As a result, KRAG, PTPN1, KRAS2, PTHLH, BCLX, DEK, IGFBP1, MYC, Livin-2, PVT1, PRex1, BCAS1, TFAP2C, EGFR, TGIF2, TNFRSF5, TNFRSF6B, EIF4G, PMS2, HCK, MYBL2, ELM02, PCTK1, CDC2L1, CDC10, TCRG, GLI3, PPP1A, ZNF217, and SRC genes were found (Table 2). The amplification of these genes was detected in 50 to 64% of the pancreatic carcinoma cell lines tested herein.
*Percentage of cell lines in which not less than 2-fold gene amplification was detected.
As a gene having a Ratio value of 4 or more, that is, a gene in which not less than 4 fold amplification was detected compared to that in a normal cell, SUPTSH, AKT2, TRRAP, Smurf1, PDAP1, MYC, PVT1, KRAS2, KRAG and MIA genes were detected (Table 3). High-level amplification of the group of genes was observed in 4 to 16% of the cell lines.
*Percentage of cell lines in which gene amplification was detected.
Next, as a gene having a Ratio value reduced to 0.75 or less in a pancreatic carcinoma cell, that is, a gene determined as a heterozygote, MTAP, DCC, CDKN2A (p16), N33, AAC1, SMAD4-2, GRP, TEK, D8S504, NAT2, LZTS1, TNFRSF10B, D9S913, GASC1, FVT1, MAP3K7, DLC1, MALTI, stSG42796, BAIAP1, BLK, LPL, NRG1, MLLT3, MADH2, SCCA1, SCCA2, NKX3A, SMAD7, MLL1, PI5, Casp3, SSXT, BCL2, JAK2, PTPRG, VIM, stSG27915, RH68621, CTDP1, SHGC-145820, EEF1E1, ESR1, and KLF12 genes were found (Table 4). A heterozygous deletion of these genes was detected with a high frequency of 50 to 82% of pancreatic carcinoma cell lines tested herein.
*Percentage of cell lines in which gene deletion was detected.
Furthermore, as a gene having a Ratio value of 0.25 or less, that is, a gene in which a homozygous deletion was detected, CDKN2A(p16), MTAP, N33, MLLT3, TEK, DEC1, CDH23, and SMAD4-2 genes were found (Table 5). A group of genes having heterozygote and homozygote significantly decreases in expression level, which may possibly be a cause of cancer.
*Percentage of cell lines in which a homozygous deletion was detected.
CDKN2A (p 16) gene was ligated downstream Survivin promoter and integrated into a Sendai virus vector. The resultant viral DNA was packaged to produce a recombinant virus. The recombinant virus was purified by discontinuous iodixanol gradient centrifugation and a heparin agarose column. Squamous cell carcinoma was inoculated in a 96 well tissue culture plate at a concentration of 5×103 cell/well and incubated in a CO2 incubator at 37° C. for one day. Then, 100 moi of purified recombinant Sendai virus was infected per well and incubated for 72 hours. The amplification level of cells was determined by a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay using a commercially available kit (manufactured by Promega, Tokyo) in accordance with the instruction. As a result, in a cell infected with the virus having CDKN2A (p16) gene integrated therein, significant inhibition of proliferation was observed. The cell extraction solution was subjected to Western blot analysis. CDKN2A (p16) protein was not detected in a control Sendai virus infection cell, whereas a clear band of CDKN2A (p16) protein was detected from the cell extraction solution sample. From the results, it was demonstrated that proliferation of carcinoma cells is suppressed by infecting the cells with Sendai virus having CDKN2A (p16) gene integrated therein. This means that Sendai virus having CDKN2A (p16) gene integrated therein can be used for reducing carcinoma or suppressing minute metastasis.
Next, a nude mouse was inoculated with squamous cell carcinoma (cells), and simultaneously, infected with 3×1011 moi of purified recombinant Sendai virus. Inhibition of carcinoma proliferation was monitored while expecting an increase of the life time of the mouse, in other words, an increase of efficiency of the gene therapy according to the present invention.
Based on the results, a clinical trial of gene therapy for a human patient can be planned.
According to the present invention, a cancer-associated gene to be used as an index for detecting canceration of a cell and degree of malignancy of cancer was found, and a method of detecting cancer using the cancer-associated gene as an index was provided, and furthermore a suppression/therapeutic method of cancer using the cancer-associated gene as essential part was provided.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2005-304497 | Nov 2005 | JP | national |
