Allelic deletion on chromosome 17p13.3 in early ovarian cancer

Cancer Research

Volumn 56, Issue 3, 1996, Pages 606-611

  Phillips, Nancy J ^a,c   Ziegler, Michelle R ^a   Radford, Diane M ^b   Fair, Keri L ^b   Steinbrueck, Todd ^b   Xynos, Francisco P ^a   Donis Keller, Helen ^b  

^a SAINT LOUIS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c SAINT LOUIS UNIVERSITY HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; MICROSATELLITE DNA;

ADULT; AGED; ALLELE; ARTICLE; CANCER STAGING; CHROMOSOMAL LOCALIZATION; CHROMOSOME 17P; CHROMOSOME DELETION; EPITHELIUM TUMOR; FEMALE; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; OVARY CANCER; PHENOTYPE; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

ADULT; AGED; AGED, 80 AND OVER; ALLELES; BASE SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 17; DNA, NEOPLASM; FEMALE; GENE DELETION; GENES, P53; GENES, TUMOR SUPPRESSOR; HETEROZYGOTE; HUMANS; MIDDLE AGED; MOLECULAR SEQUENCE DATA; OVARIAN NEOPLASMS;

EID: 0030024245     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (44)

1. Fearon, E R , and Vogelstein, B. A genetic model for colorectal tumorigenesis Cell, 61. 759-767, 1990.
2. Cliby, W., Ritland, S , Hartmann, L., Dodson, M., Halling, K. C., Keeney, G., Podratz, K. C , and Jenkins, R. B Human epithelial ovarian cancer allelotype. Cancer Res. 55: 2393-2398, 1993.
3. Sato, T , Saito, H., Morita, R., Koi, S., Lee, J. H., and Nakamura, Y. Allelotype of human ovarian cancer. Cancer Res., 51: 5118-5122, 1991.
4. Yang-Feng, T. L., Han, H., Chen, K-C , Li, S-L., Claus, E. B., Carcangiu, M. L., Chambers, S. K., Chambers, J. T., and Schwartz, P. E. Allelic loss in ovarian cancer. Int J. Cancer, 54: 546-551, 1993
5. Foulkes, W D., Black, D. M., Stamp, G. W H., Solomon, E , and Trowsdale, J. Very frequent loss of heterozygosity throughout chromosome 17 in sporadic ovarian carcinoma Int. J. Cancer. 54: 220-225, 1993.
6. Pieretti, M., Powell, D. E , Gallion, H. H., Case, E. A., Conway, P. S., and Turker, M. S. Genetic alterations on chromosome 17 distinguish different types of epithelial ovarian tumors. Hum. Pathol., 26: 393-397, 1995.
7. Phillips, N. J., Ziegler, M , Saha, B., and Xynos, F. Allelic loss on chromosome 17 in human ovarian cancer. Int. J. Cancer, 54: 85-91, 1993.
8. Tavassoli, M., Ruhrberg, C., Beaumont, V., Reynolds, K., Kirkham, N., Collins, W. P., and Farzaneh, F. Whole chromosome 17 loss in ovarian cancer Genes Chromosomes & Cancer, 8: 195-198, 1993
9. Jacobs, I. J., Smith, S. A., Wiseman, R. W., Futreal, P. A., Harrington, T., Osborne, R. J., Leech, V., Molyneux, A., Berchuck, A., Ponder, B. A J , and Bast, R. C., Jr. A deletion unit on chromosome 17q in epithelial ovarian tumors distal to the familial breast/ovarian cancer locus. Cancer Res., 53: 1218-1221, 1993.
10. Okamoto, A , Sameshima, Y., Yokoyama, S , Terashima, Y , Sugimura, T , Terada, M , and Yokota, J. Frequent allelic losses and mutations of the p53 gene in human ovarian carcinoma. Cancer Res., 51: 5171-5176, 1991.
11. Kupryjanczyk, J., Thor, A. D., Beauchamp, R., Merritt, V., Edgerton, S. M., Bell, D. A., and Yandell, D. W. p53 gene mutations and protein accumulation in human ovarian cancer. Proc. Natl. Acad. Sci. USA, 90: 4961-4965, 1993.
12. Kupryjanczyk, J., Bell, D. A., Dimeo, D., Beauchamp, R., Thor, A D., and Yandell, D. W. p53 gene analysis of ovarian borderline tumors and stage 1 carcinomas Hum Pathol., 26: 387-392, 1995.
13. Milner, B J., Allan, L. A., Eccles, D. M., Kitchener, H. C , Leonard, R C. F., Kelly, K. F., Parker, D. E., and Haites, N. E. p53 mutation is a common genetic event in ovarian carcinoma. Cancer Res, 53: 2128-2132, 1993.
14. Teneriello, M. G., Ebina, M., Linnoila, R. I., Henry, M , Nash, J. D., Park, R. C , and Birrer, M. J. p53 and Ki-ras gene mutations in epithelial ovarian neoplasms Cancer Res., 53: 3103-3108, 1993.
15. Aaltonen, L. A , Peltomaki, P., Leach, F. S., Sistonen, P., Pylkkanen, L., Mecklin, J-P., Jarvinen, H., Powell, S. M., Jen, J., Hamilton, S. R., Peterson, G. M., Kinzler, K. W , Vogelstein, B , and de la Chapelle, A. Clues to the pathogenesis of familial colorectal cancer. Science (Washington DC), 260: 812-816, 1993.
16. Thibodeau, S. N., Bren, G., and Schaid, G Microsatellite instability in cancer of the proximal colon. Science (Washington DC), 260. 816-819, 1993.
17. Risinger, J. I., Berchuck, A., Kohler, M. F., Watson, P., Lynch, H. T., and Boyd, J. Genetic instability of microsatellites in endometrial carcinoma. Cancer Res., 53: 5100-5103, 1993.
18. Fishel, R., Lescoe, M. R., Rao, M. R. S., Copeland, N. G., Jenkins, N. A , Garber, J., Kaue, M., and Kolodner, R. The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer. Cell, 75: 1027-1038, 1993.
19. Watson, P , and Lynch, H. T Extracolonic cancer in hereditary nonpolyposis colorectal cancer Cancer (Phila.), 71. 677-685, 1993.
20. Radford, D. M , Fair, K. L., Phillips, N. J., Ritter, J. H., Steinbrueck, T., Holt, M. S., and Donis-Keller, H. Allelotyping of ductal carcinoma in situ of the breast: deletion of loci on 8p, 13q, 16q, 17p, and 17q. Cancer Res., 55: 3399-3406, 1995.
21. McDonald, J. D., Daneshvar, L , Willert, J. R., Matsumura, K., Waldman, F., and Cogen, P. H. Physical mapping of chromosome 17p13.3 in the region of a putative tumor suppressor gene important in medulloblastoma. Genomics, 23: 229-232, 1994.
22. Williamson, R , Bowcock, A , Kidd, K., Pearson, P., Schmidtke, J., Ceverha, P., Chipperfield, M., Cooper, D. N , Coutelle, C , Hewitt, J , Klinger, K , Langley, K., Beckmann, J., Tolley, M., and Maidak, B. Human gene mapping 11 Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR, and DNA polymorphisms. Cytogenet. Cell Genet., 58: 1548-1569, 1991.
23. Fain, P. R., Ledbetter, D. H., and Solomon, E. Proceedings of the Second International Workshop on Human Chromosome 17 Mapping 1991 Cytogenet. Cell Genet., 57. 65-77, 1991
24. Guzzetta, V. Montes de Oca-Luna, R., Lupski, J R , and Patel, P. L Isolation of region-specific and polymorphic markers from chromosome 17 by restricted Alu polymerase chain reaction Genomics, 9. 31-36, 1991.
25. Jones, M. H , and Nakamura, Y Detection of loss of heterozygosity at the human TP53 locus using a dinucleotide repeat polymorphism. Genes Chromosomes & Cancer, 5: 89-90, 1992.
26. Hall, J M , Friedman, L., Guenther, C., Lee, M. K., Weber, J. L., Black, D M , and King, M-C. Closing in on a breast cancer gene on chromosome 17q. Am. J. Hum. Genet., 50, 1235-1242, 1992.
27. Carrozzo, R., and Ledbetter, D. H. Dinucleotide repeat polymorphism mapping to the critical region for lissencephaly (17p13.3) Hum. Mol. Genet., 2: 615, 1993
28. Gerken, S. C , Albertsen, H., Elsner, T., Ballard, L., Holik, P., Lawrence, E., Moore, M., Zhao, X., and White, R. A strategy for constructing high-resolution genetic maps of the human genome: a genetic map of chromosome 17p, ordered with meiotic breakpoint-mapping panels. Am. J. Hum. Genet., 56: 484-499, 1995.
29. Fain, P. R. Report of the Third International Workshop on Human Chromosome 17 Mapping 1992. Cytogenet Cell Genet., 60: 177-186, 1992.
30. Tombran-Tink, J., Pawar, H., Swaroop, A., Rodriguez, I., and Chader, G. J. Localization of the gene for pigment epithelium-derived factor (PEDF) to chromosome 17p13 1 and expression in cultured human retinoblastoma cells. Genomics, 19: 266-274, 1994.
31. Matsuda, M., Tanaka, S., Nagata, S., Kojima, A., Kurata, T., and Shibuya, M. Two species of human CRK cDNA encode proteins with distinct biological activities. Mol. Cell Biol , 12, 3482-3489, 1992.
32. Ledbetter, D H , Ledbetter, S A., van Tuinen, P , Summers, K M., Robinson, T. J., Nakamura, Y., Wolf, R., White, R., Barker, D. F., Wallace, M. R., Collins, F. S., and Dobyns, W. B. Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome region. Proc. Natl. Acad. Sci. USA, 86: 5136-5140, 1989.
33. Andersen, T I., Gaustad, A , Ottestad, L , Farrants, G. W., Nesland, J. M , Tveit, K. M., and Borresen, A-L. Genetic alterations of the tumor suppressor gene regions 3p, 11p, 13q, 17p, and 17q in human breast carcinomas. Genes Chromosomes & Cancer. 4: 113-121, 1992.
34. Sato, T., Akiyama, F., Sakamoto, G., Kasumi, F., and Nakamura, Y. Accumulation of genetic alterations and progression of primary breast cancer. Cancer Res., 51: 5794-5799, 1991.
35. Cogen, P. H , Daneshvar, L., Metzger, A. K., Duyk, G., Edwards, M. S. B , and Sheffield, V. C. Involvement of multiple chromosome 17p loci in medulloblastoma tumorigenesis. Am. J. Hum. Genet., 50: 584-589, 1992.
36. Makos Wales, M., Biel, M. A., El Diery, W., Nelkin, B. D., Issa, J-P., Cavenee, W K., Kuerbitz, S J., and Baylin, S. B. p53 activates expression of HIC-1, a new candidate tumor suppressor gene on 17p13.3. Nat. Med., 1: 570-577, 1995.
37. Schultz, D. C., Vanderveer, L., Berman, D., Hamilton, T. C , Wong, A. J., and Godwin, A. K A candidate tumor suppressor gene for ovarian cancer on chromosome 17p13.3 (Abstract). Am. J. Human Genet., 57: A4, 1995.
38. Pieretti, M , Powell, D E., Gallion, H. H., Conway, P. S , and Turker, M. S. Hypermethylation at a chromosome 17 "hot spot" is a common event in ovarian cancer Hum. Pathol., 26: 398-401, 1995.
39. Mok, S. C-H., Bell, D. A , Knapp, R. C., Fishbaugh, P M., Welch, W R., Muto, M G., Berkowitz, R. S., and Tsao, S-W. Mutation of K-ras protooncogene in human ovarian epithelial tumors of borderline malignancy Cancer Res., 53: 1489-1492, 1993.
40. Tsao, S-W., Mok, C-H., Oike, K., Muto, M., Goodman, H M , Sheets, E E., Berkowitz, R. S., Knapp, R. C., and Lau, C. C. Involvement of p53 gene in the allelic deletion of chromosome 17p in human ovarian tumors. Anticancer Res., 11: 1975-1982, 1991.
41. Eccles, D. M., Cranston, G., Steel, C. M., Nakamura, Y , and Leonard, R. C. F Allele losses on chromosome 17 in human epithelial ovarian carcinoma. Oncogene, 5: 1599-1601, 1990.
42. Merajver, S. D., Pham, T M., Caduff, R. F., Chen, M., Poy, E. L., Cooney, K. A., Weber, B A., Collins, F C., Johnston, C., and Frank, T. S Somatic mutations in the BRCA1 gene in sporadic ovarian tumours Nat. Genet., 9, 439-443, 1995.
43. Takahashi, H., Behbakht, K., McGovern, P. E , Chiu, H-C , Couch, F J., Weber, B L , Friedman, L. S , King, M-C , Furusato, M., LiVolsi, V. A , Meozin, A. W., Liu, P. C., Benjamin, I , Morgan, M. A., King, S A., Rebane, B A., Cardonick, A., Mikuta, J. J., Rubin, S. C., and Boyd, J. Mutation analysis of the BRCA1 gene in ovarian cancers Cancer Res., 55: 2998-3002, 1995.
44. Hosking, L., Trowsdale, J., Nicolai, H., Solomon, E., Foulkes, W., Stamp, G., Signer, E., and Jeffreys. A. A somatic BRCA1 mutation in an ovarian tumor. Nat Genet., 9: 343-344, 1995