Evidence for a tumor suppressor gene distal to BRCA1 in prostate cancer

Journal of Urology

Volumn 155, Issue 2, 1996, Pages 720-725

  Williams, Briana J ^a   Jones, Emma ^a   Zhu, Xiao Lin ^a   Steele, Michael R ^a   Stephenson, Robert A ^a   Rohr, L Ralph ^a   Brothman, Arthur R ^a  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

chromosome deletion; genes, suppressor, tumor; in situ hybridization; prostatic neoplasms

Indexed keywords

ARTICLE; CANCER GENETICS; CANCER RISK; CHROMOSOME 17Q; GENE DELETION; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; PRIORITY JOURNAL; PROSTATE CANCER; RISK ASSESSMENT; TUMOR SUPPRESSOR GENE;

EID: 0030046741     PISSN: 00225347     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-5347(01)66509-1     Document Type: Article

References (38)

1. Phillips, S. M. A., Morton, D. G., Lee, S. J., Wallace, D. M. A. and Neoptolemos, J. P.: Loss of heterozygosity of the retinoblastoma and adenomatous polyposis susceptibility gene loci and in chromosomes 10p, 10q, and 16q in human prostate cancer. Br. J. Urol., 73: 390, 1994.
2. Brewster, S. F., Browne, S. and Brown, K. W.: Somatic allelic loss at the DCC, APC, nm23-H1 and p53 tumor suppressor gene loci in human prostatic carcinoma. J. Urol., 151: 1073, 1994.
3. Gao, X., Honn, V., Grignon, D., Sakr, W. and Chen, Y. Q.: Frequent loss of expression and loss of heterozygosity of the putative tumor suppressor gene DCC in prostatic carcinoma. Cancer Res., 53: 2723, 1993.
4. Brooks, J. D., Bova, G. S. and Isaacs, W. B.: Allelic loss of the retinoblastoma gene in primary human prostatic adenocarcinomas. Prostate, 26: 35, 1995.
5. Rubin, S. J., Hallahan, D. E., Ashman, C. R., Brachman, D. G., Beckett, M. A., Virudachalam, S., Yandell, D. W. and Weichselbaum, R. R.: Two prostate carcinoma cell lines demonstrate abnormalities in tumor suppressor genes. J. Surg. Oncol., 46: 31, 1991.
6. Isaacs, W. B., Carter, B. S. and Ewing, C. M.: Wild-type p53 suppresses growth of human prostate cancer cells containing mutant p53 alleles. Cancer Res., 51: 4716, 1991.
7. Effert, P. J., Neubauer, A., Walther, P. J. and Liu, E. T.: Alterations of the p53 gene are associated with the progression of a human prostate carcinoma. J. Urol., 147: 789, 1992.
8. Latil, A., Baron, J.-C., Cussenot, O., Fournier, G., Soussi, T., Boccon-Gibod, L., LeDuc, A., Rouesse, J. and Lidereau, R.: Genetic alterations in localized prostate cancer: identification of a common region of deletion on chromosome arm 18q. Genes Chromosom. Cancer, 11: 119, 1994.
9. Visakorpi, T., Kallioniemi, A. H., Syvanen, A.-C., Hyytinen, E. R., Karhu, R., Tammela, T., Isola, J. J., and Kallioniemi, O.-P.: Genetic changes in primary and recurrent prostate cancer by comparative genomic hybridization. Cancer Res., 55: 342, 1995.
10. Zenklusen, J. C., Thompson, J. C., Troncoso, P., Kagan, J. and Conti, C. J.: Loss of heterozygosity in human primary prostate carcinomas: a possible tumor suppressor gene at 7q31.1. Cancer Res., 54: 6370, 1994.
11. Ichikawa, T., Ichikawa, Y., Dong, J., Hawkins, A. L., Griffin, C. A., Isaacs, W. B., Oshimura, M., Barrett, J. C. and Isaacs, J. T.: Localization of metastasis suppressor gene(s) for prostate cancer to the short arm of human chromosome 11. Cancer Res., 52: 3486, 1992.
12. Rinker-Schaeffer, C. W., Hawkins, A. L., Ru, N., Dong, J., Stoica, G., Griffin, C. A., Ichikawa, T., Barrett, J. C. and Isaacs, J. T.: Differential suppression of mammary and prostate cancer metastasis by human chromosomes 17 and 11. Cancer Res., 54: 6249, 1994.
13. Berube, N. G., Speevak, M. D. and Chevrette, M.: Suppression of tumorigenicity of human prostate cancer cells by introduction of human chromosome del(12)(q13). Cancer Res., 54: 3077.
14. Bova, G. S., Carter, B. S., Bussemakers, M. J. G., Emi, M., Fujiwara, Y., Kyprianou, N., Jacobs, S. C., Robinson, J. C., Epstein, J. I., Walsh, P. C. and Isaacs, W. B.: Homozygous deletion and frequent allelic loss of chromosome 8p22 loci in human prostate cancer. Cancer Res., 53: 3869, 1993.
15. MacGrogan, D., Levy, A., Bostwick, D., Wagner, M. and Bookstein, R.: Loss of chromosome arm 8p loci in prostate cancer: mapping by quantitative allelic imbalance. Genes Chromosom. Cancer, 10: 151, 1994.
16. Morton, R. A., Ewing, C. M., Nagafuchi, A., Tsukita, S. and Isaacs, W. B.: Reduction of E-cadherin levels and deletion of the α-catenin gene in human prostate cancer cells. Cancer Res., 53: 3585, 1993.
17. Eagle, L. R., Yin, X., Brothman, A. R., Williams, B. J., Atkin, N. B. and Prochownik, E. V.: Mutation of the MXI1 gene in prostate cancer. Nature Genet., 9: 249, 1995.
18. 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 chromosomes 16q and 10q in human prostate cancer. Proc. Natl. Acad. Sci, U.S.A., 87: 8751, 1990.
19. Bergerheim, U. S. R., Kunimi, K., Collins, V. P. and Ekman, P.: Deletion mapping of chromosomes 8, 10, and 16 in human prostatic carcinoma. Genes Chromosom. Cancer, 3: 215, 1991.
20. Macoska, J. A., Trybus, T. M., Sakr, W. A., Wolf, M. C., Benson, P. D., Powell, I. J. and Pontes, J. E.: Fluorescence in situ hybridization analysis of 8p allelic loss and chromosome 8 instability in human prostate cancer. Cancer Res., 54: 3824, 1994.
21. Matsuyama, H., Pan, Y., Skoog, L., Tribukait, B., Naito, K., Ekman, P., Lichter, P. and Bergerheim, U. S. R.: Deletion mapping of chromosome 8p in prostate cancer by fluorescence in situ hybridization. Oncogene, 9: 3071, 1994.
22. Cher, M. L., Ito, T., Weidner, N., Carroll, P. R. and Jensen, R. H.: Mapping of regions of physical deletion on chromosome 16q in prostate cancer cells by fluorescence in situ hybridization (FISH). J. Urol., 153: 249, 1995.
23. Miki, Y., Swensen, J., Shattuck-Eidens, D., Futreal, P. A., Harshman, K., Tavtigian, S., Liu, Q., Cochran, C., Bennett, L. M., Ding, W., Bell, R., Rosenthal, J., Hussey, C., Tran, T., McClure, M., Frye, C., Hattier, T., Phelps, R., Haugen-Strano, A., Katcher, H., Yakumo, K., Gholami, Z., Shaffer, D., Stone, S., Bayer, S., Wray, C., Bogden, R., Dayananth, P., Ward, J., Tonin, P., Narod, S., Bristow, P. K., Norris, F. H., Helvering, L., Morrison, P., Rosteck, P., Lai, M., Barrett, J. C., Lewis, C., Neuhausen, S., Cannon-Albright, L., Goldgar, D., Wiseman, R., Kamb, A. and Skolnick, M. H.: A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science, 266: 66, 1994.
24. Arason, A., Barkadottir, T. B. and Egilsson, V.: Linkage analysis of chromosome 17q markers and breast-ovarian cancer in Icelandic families, and possible relationship to prostatic cancer. Am. J. Hum. Genet., 52: 711, 1993.
25. Tulinius, H., Egilsson, V., Olafsdottir, G. H. and Sigvaldson, H.: Risk of prostate, ovarian, and endometirial cancer among relatives of women with breast cancer. Br. Med. J., 305: 855, 1992.
26. Ford, D., Easton, D. F., Bishop, D. T., Narod, S. A. and Goldgar, D. E.: Risks of cancer in BRCA1 mutation carriers. Lancet, 343: 692, 1994.
27. Brothman, A. R., Watson, M. J., Zhu, X. L., Williams, B. J. and Rohr, L. R.: Evaluation of 20 archival prostate tumor specimens by fluorescence in situ hybridization (FISH). Cancer Genet. Cytogenet., 75: 40, 1994.
28. Jones, E., Zhu, X. L., Rohr, L. R., Stephenson, R. A. and Brothman, A. R.: Aneusomy of chromosome 7 and 17 detected by FISH in prostate cancer and the effects of in vitro selection. Genes Chromosom. Cancer, 11: 163, 1994.
29. Brothman, A. R., Steele, M. R., Williams, B. J., Jones, E., Odelberg, S., Albertsen, H. M., Rohr, L. R. and Stephenson, R. A.: Loss of chromosome 17 loci in prostate cancer detected by polymerase chain reaction quantitation of allelic markers. Genes Chromosom. Cancer, 13: 278, 1995.
30. Murakami, Y., Brothman, A. R., Leach, R. and White, R.: Suppression of malignant phenotype in a human prostate cancer cell line by fragments of normal chromosome 17q. Cancer Res., 55: 338.
31. Konig, J. J., Teubel, W., van Dongen, J. W., Hagemeijer, A., Romijn, J. C. and Schröder, F. H.: Tissue culture loss of aneuploid cells from carcinomas of the prostate. Genes Chromosom. Cancer, 8: 22, 1993.
32. Pierce, J. C., Sauer, B. and Sternberg, N.: A positive selection vector for cloning high molecular weight DNA by the bacteriophage P1 system: improved cloning efficiency. Proc. Natl. Acad. Sci. U.S.A., 89: 2056, 1992.
33. Albertsen, H., Smith, S. A., Mazoyer, S., Fujimoto, E., Stevens, J., Williams, B., Rodriguez, P., Cropp, C. S., Slijepcevic, P., Carlson, M., Robertson, M., Bradley, P., Lawrence, E., Harrington, T., Sheng, Z. M., Hoopes, R., Sternberg, N., Brothman, A., Callahan, R., Ponder, B. A. J. and White, R.: A physical map and candidate genes in the BRCA1 region of chromosome 17q12-21. Nature Genetics, 7: 472, 1994.
34. Birnboim, H. C. and Doly, J.: A rapid alkaline extraction procedure for screening recombinant plasmid DNA. Nucleic Acids Res., 7: 1513, 1979.
35. Sokal, R. R. and Rohlf, F. J.: Biometry. San Francisco: W. H. Freeman and Company, 2nd ed., chapt. 7, 1981.
36. Devore, J. L.: Probability and Statistics for Engineering and the Sciences. Belmont: Wadsworth, Inc., 3rd ed., p. 482, 1991.
37. Brown, J. A., Alcarez, A., Takahashi, S., Persons, D. L., Lieber, M. M. and Jenkins, R. B.: Chromosomal aneusomies detected by fluorescent in situ hybridization (FISH) analysis in clinically localized prostate carcinoma. J. Urol., 152: 1157, 1994.
38. Williams, B. J., Jones, E. and Brothman, A. R.: Homologous centromere association of chromosomes 9 and 17 in prostate cancer. Cancer Genet. Cytogenet., 85: 143, 1995.