Chromosome 3p24-26 and 3-22-12 loss in human prostatic adenocarcinoma

International Journal of Cancer

Volumn 71, Issue 1, 1997, Pages 20-25

  Dahiya, Rajvir ^a   McCarville, Joseph ^a   Hu, Weixing ^a   Lee, Celeste ^a   Chui, Richard M ^a   Kaur, Gurjit ^a   Deng, Guoren ^a  

^a VETERANS AFFAIRS MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 3P; CHROMOSOME DELETION; CHROMOSOME LOSS; CLINICAL ARTICLE; HUMAN; HUMAN TISSUE; MALE; PRIORITY JOURNAL; PROSTATE ADENOCARCINOMA;

ADENOCARCINOMA; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 3; HETEROZYGOTE; HUMANS; MALE; NEOPLASM STAGING; PROSTATIC NEOPLASMS;

EID: 0030935162     PISSN: 00207136     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0215(19970328)71:1<20::AID-IJC5>3.0.CO;2-5     Document Type: Article

References (26)

1. ANAMTHAWAT-JONSSON, K., EYFJORD, J.E., OGMUNDSDOTTIR, H.M., PETURSDOTTIR, I. and STEINARSDOTTIR, M., Instability of chromosome 1, 3, 16, and 17 in primary breast carcinomas inferred by fluorescence in situ hybridization. Cancer Genet. Cytogenet., 88, 1-7 (1996).
2. ARLT, M.F., HERZOG, T.J., MUTCH, D.G. and GOODFELLOW, P.J., Loss of heterozygosity of chromosome 3p sequence is an infrequent event in endometrial cancer. Gynecol. Oncol., 60, 308-312 (1996).
3. ARPS, S., RODEWALD, A., SCHMALENBERGER, B., CARL, P., BRESSEL, M. and KASTENDIECK, H., Cytogenetic survey of 32 cancers of the prostate. Cancer Genet. Cytogenet., 66, 93-99 (1993).
4. CANNON-ALBRIGHT, L. and EELES, R., Progress in prostate cancer. Nature (Genet.), 9, 336-338 (1995).
5. CARTER, B.S., EWING, C.M., WARD, W.S., TREIGER, B.F., AALDERS, T.W., SCHALKEN, J.A., EPSTEIN, J.I. and ISAACS, W.B., Allelic loss of chromosome 16q and 10q in human prostate cancer. Proc. nat. Acad. Sci. (Wash.), 87, 8751-8755 (1990).
6. CUNNINGHAM, J.M., SHAN, A., WlCK, M.J., MCDONNELL, S.K., SCHAID, D.J., TESTER, D.J., QIAN, J., TAKAHASHI, S., JENKINS, R.B., BOSTWICK, D.G. and THIBODEAU, S.N., Allelic imbalance and microsatellite instability in prostatic adenocarcinoma. Cancer Res., 56, 4475-4482 (1996).
7. DAHIYA, R., DENG, G., CHEN, K., HAUGHNEY, P.C., CUNHA, G.R. and NARAYAN, P., p53 tumor-suppressor gene mutations are mainly localised on exon 7 in human primary and metastatic prostate cancer. Brit. J. Cancer, 74, 264-268 (1996).
8. DAHIYA, R., DENG, G., CHEN, K., HAUGHNEY, P.C., CUNHA, G.R. and NARAYAN, P., New approach to hot-start polymerase chain reaction using Taq DNA polymerase antibody. Urol. Oncol., 1, 42-46 (1995).
9. EGAWA, S., UCHIDA, T., SUYAMA, K., WANG, C., OHORI, M., IRIE, S., IWAMURA, M. and KOSHIBA, K., Genetic instability of microsatellite repeats in prostate cancer: relationship to clinopathological variables. Cancer Res., 55, 2418-2421 (1995).
10. EMMERT-BUCK, M.R., VOCKE, C.D., POZZATTI, R.O., DURAY, P.H., JENNINGS, S.B., FLORENCE, C.D., ZHUANG, Z., BOSTWICK, D.G., LIOTTA, L.A. and LINEHAN, W.M., Allelic loss of chromosome 8p12-21 in microdissected prostatic intraepithelial neoplasia. Cancer Res., 55, 2959-2962 (1995).
11. GAO, X., ZACHAREK, A., SALKOWSKI, A., GRIGNON, D.J., SAKR, W., PORTER, A.T. and HONN, K.V., Loss of heterozygosity of the BRCA1 and other loci on chromosome 17q in human prostate cancer. Cancer Res., 55, 1002-1005 (1995).
12. HOSOE, S., SHIGEDO, Y., UENO, K., TACHIBANA, I., OSAKI, T., TANIO, Y., KAWASE, I., YAMAKAWA, K., NAKAMURA, Y. and KISHIMOTO, T., Detailed deletion mapping of the short arm of chromosome 3 in small-cell carcinoma of the lung. Lung Cancer, 10, 297-305 (1994).
13. Joos, S., BERGERHEIM, S.R., MATSUYAMA, H., BENTZ, M., MANSOIR, S. and LICHTER, P., Mapping of chromosomal gains and losses in prostate cancer by comparative genomic hybridization. Genes Chromosomes Cancer, 14, 267-276 (1995).
14. LATIF, F., FIVASH, M. and GNARRA, J., Identification of the von Hippel-Lindau disease tumor suppressor gene. Science, 260, 1317-1320 (1993).
15. MAESTRO, R., GASPAROTTO, D., VUKOSALJEVIC, T., BARZAN, L., SULFARQ, S. and BOIOCCHI, M., Three discrete regions of deletion at 3p in head and neck cancers. Cancer Res., 53, 5775-5779 (1993).
16. OHMURA, H., TAHARA, H., SUZUKI, M., IDE, T., SHIMIZU, M., YOSHIDA, M.A., TAHARA, E., SHAY, J.W., BARRETT, J.C. and OSHIMURA, M., Restoration of the cellular senescence program and repression of telomerase by human chromosome 3. Jap. J. Cancer Res., 86, 899-904 (1995).
17. PAPADOPOULOS, N. and 19 OTHERS, Mutation of a mutL homolog in hereditary colon cancer. Science, 263, 1625-1629 (1994).
18. SATOH, H., LAMB, P.W., DONG, J.T., EVERITT, J., BOREIKO, C., OSHIMURA, M. and BARRETT, J.C., Suppression of tumorigenicity of A549 lung adenocarcinoma cells by human chromosome 3 and 11 introduced via microcell-mediated chromosome transfer. Mol. Carcinogenesis, 7, 157-164 (1993).
19. SEKIDO, Y., BADER, S., LATIF, F., CHEN, J.Y., DUH, P.M., WEI, M.H., ALBANESI, J.P., LEE, C.C., LERMAN, M.I. and MINNA, J.D., Human semaphorins A (V) and IV reside in the 3p21.3 small cell lung deletion region and demonstrate distinct expression patterns. Proc. nat, Acad. Sci. (Wash.), 93, 4120-4125 (1996).
20. SOZZI, G. and 13 OTHERS, The FHIT gene at 3p14.2 is abnormal in lung cancer. Cell 85, 17-26 (1996).
21. THIBERVILLE, L., BOURGUIGNON, J., METAYER, J., BOST, F., DIARRA-MEHRPOUR, M., BIGNON, J., LAM, S., MARTIN, J.-P. and NOUVET, G., Frequency and prognostic evaluation of 3p21-22 allelic losses in non-small cell lung cancer, Int. J. Cancer, 64, 371-377 (1995).
22. WABER, P.G., LEE, N.K. and NISEN, P.D., Frequent allelic loss at chromosome arm 3p is distinct from genetic alterations of the von Hippel-Lindau tumor suppressor gene in head and neck cancer. Oncogene. 12, 365-369 (1996).
23. WATANABE, M., IMAI, H., SHIRAISHI, T., SHIMAZAKI, J., KOTAKE, T. and YATANI, R., Microsatellite instability in human prostate cancer. Brit. J. Cancer, 72, 562-564 (1995).
24. WEI, M.-H., and 14 OTHERS. Construction of a 600-kilobase cosmid clone contig and generation of a transcriptional map surrounding the lung cancer tumor suppressor gene (TSG) locus on human chromosome 3p21.3: progress toward the isolation of a lung cancer TSG. Cancer Res., 56, 1487-1492 (1996).
25. WEINBERG, R.A.,Tumor suppressor genes. Science, 254, 1138-1146 (1991).
26. WHANG-PENG, J., KAO-SHAH, C.S., LEE, E.G., BUNN, P.J., CARNEY, D.N., GAZDAR, A. and MINNA, J.D., A specific chromosome defect associated with human small-cell lung cancer: deletion 3p14-3p23. Science, 215, 181-182 (1982).