Microsatellite analysis of endometriosis reveals loss of heterozygosity at candidate ovarian tumor suppressor gene loci

Cancer Research

Volumn 56, Issue 15, 1996, Pages 3534-3539

  Jiang, Xiuxian ^a   Hitchcock, Andrew ^b   Bryan, Emma J ^a   Watson, Richard H ^a   Englefield, Patricia ^a   Thomas, Eric J ^a   Campbell, Ian G ^a  

^a UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

^b SOUTHAMPTON GENERAL HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

MICROSATELLITE DNA;

ARTICLE; CANCER RISK; ENDOMETRIOSIS; ENDOMETRIUM; FEMALE; GENE LOCUS; GENE REPRESSION; GENETIC ANALYSIS; HUMAN; HUMAN TISSUE; OVARY TUMOR; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

BASE SEQUENCE; CLONE CELLS; DNA, NEOPLASM; DNA, SATELLITE; ENDOMETRIOSIS; FEMALE; GENE DELETION; GENE EXPRESSION REGULATION, NEOPLASTIC; GENES, P53; GENES, TUMOR SUPPRESSOR; HETEROZYGOTE; HUMANS; MICROSATELLITE REPEATS; MOLECULAR SEQUENCE DATA; MUTATION; OVARIAN NEOPLASMS; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;

EID: 0029684011     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (36)

1. Thomas, E. J. Endometriosis: still an enigma. Br. J. Obstet. Gynaecol., 100: 615-617, 1993.
2. Martin, D. C., Ahmic, R., Elzeky, F. A., Vanderzwaag, R., Pickens, M. T., and Cherry, K. Increased histologic confirmation of endometriosis. J. Gynecologic Surgery, 6: 275-279, 1990.
3. Brincat, M., Galea, R., Buhagiar, A. Polycystic ovaries and endometriosis: a possible connection. Br. J. Obstet. Gynaecol., 101: 346-348, 1994.
4. Mahmood, T. A., and Templeton, A. Prevalence and genesis of endometriosis. Hum. Reprod. (Oxf), 6: 544-549, 1991.
5. McMeekin, D. S., Burger, R. A., Manetta, A., Disaia, P., and Berman, M. L. Endometrioid adenocarcinoma of the ovary and its relationship to endometriosis. Gynecol. Oncol., 59: 81-86, 1995.
6. Depriest, P. D., Banks, E. R., Powell, D. E., Vannagell, J. R., Gallion, H. H., Puls, L. E., Hunter, J. E., Kryscio, R. J., and Royalty, M. B. Endometrioid carcinoma of the ovary and endometriosis, the association in postmenopausal women. Gynecol. Oncol., 47: 71-75, 1992.
7. Mostoufizadeh, M. G. H., and Scully, R. E. Malignant tumor arising in endometriosis Clin. Obstet. Gynecol., 23: 951-963, 1980.
8. De la Cuesta, R. S., Eichhorn, J. H., Rice, L. W., Fuller, A. F., Jr., Nikrui, N., and Goff, B. A. Histologic transformation of benign endometriosis to early epithelial ovarian cancer. Gynecol. Oncol., 60: 238-244, 1996.
9. Vercellini, P., Parazzini, F., Bolis, G., Carinelli, S., Dindelli, M., Vendola, N., Luchini, L., and Crosignani, P. G. Endometriosis and ovarian cancer. Am. J. Obstet. Gynecol., 169: 181-182, 1993.
10. Ballouk, F., Ross, J. S., and Wolf, B. C. Ovarian endometriotic cysts: an analysis of cytologic atypia and DNA ploidy. Am. J. Clin. Pathol., 102: 415-419, 1994.
11. Symonds, D. A., Johnson, D. P., and Wheeless, C. R. J. Feulgen cytometry in simultaneous endometrial and ovarian carcinoma. Cancer (Phila.), 61: 2511-2516, 1988.
12. Braly, P. S., and Klevecz, R. R. Flow cytometric evaluation of ovarian cancer. Cancer (Phila.), 71: 1621-1628, 1993.
13. Kennedy, S., Mardon, H., and Barlow, D. Familial endometriosis J. Assist. Reprod. Genet., 12: 32-34, 1995.
14. Coxhead, D., and Thomas, E. J. Familial inheritance of endometriosis in a British population: a case control study. J. Obstet. Gynaecol. (Bristol), 13: 42-44, 1993.
15. Fearon, E. R., and Vogelstein, B. A. A genetic model for colorectal tumorigenesis. Cell, 61: 759-767, 1990.
16. Vercellini, P., Trecca, D., Oldani, S., Fracchiolla, N. S., Neri, A., and Crosignani, P. G. Analysis of p53 and ras gene mutations in endometriosis. Gynecol. Obstet. Invest., 38: 70-71, 1994.
17. Dangel, A., Medchill, M. T., Davis, G., Meloni, A. M., and Sandberg, A. A. Cytogenetic studies in endometriosis tissue. Cancer Genet. Cytogenet., 78: 172-174, 1994.
18. Pan, L. X., Diss, T. C., Peng, H. Z., and Isaacson, P. G. Clonality analysis of defined B-cell populations in archival tissue sections using microdissection and PCR. Histopathol (Oxf). 24: 323-327, 1994.
19. Allen, R. C., Zoghbt, H. Y., Moseley, A. B., Rosenblatt, H. M., and Belmont, J. W,. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen receptor gene correlates with X- chromosome inactivation Am. J. Hum. Genet., 51: 1229-1239, 1992.
20. Milner, B. J., Allan, L. A., Eccles, D. M., Kitchener, H. C., Leonard, R. C. F., Kelly, K. F., Parkin, D. E., and Haites, N. E. p53 mutation is a common genetic event in ovarian carcinoma Cancer Res., 53: 2128-2132, 1993.
21. Campbell, I. G., Nicolai, H. M., Foulkes, W. D., Senger, G., Stamp, G. W., Allan, G., Boyer, C., Jones, K., Bast, R. C., Jr., Solomon, E., Trowsdale, J., and Black, D. M. A novel gene encoding a B-Box protein within the BRCA1 region at 17q21.1. Hum Mol. Genet., 3: 589-594, 1994.
22. Nilbert, M., Pejovic, T., Mandahl, N., Iosif, S., Willen, H., and Mitelman, F. Monoclonal origin of endometriotic cysts. Int. J. Gynecological Cancer, 5: 61-63, 1995.
23. 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., 53: 2393-2398, 1993.
24. Osborne, R. J., and Leech, V. L. PCR allelotyping of human ovarian cancer. Br. J. Cancer. 69: 429-438, 1994.
25. Englefield, P., Foulkes, W. D., and Campbell, I. G. Loss of heterozygosity on chromosome 22 in ovarian carcinoma is distal to and is not accompanied by mutations in NF2 at 22q12. Br. J. Cancer, 70: 905-907, 1994.
26. Foulkes, W. D., Stamp, G. W. H., Afzal, S., Lalani, N., McFarlane, C. P., Trowsdale, J., and Campbell, I. G. MDM2 overexpression is rare in ovarian carcinoma irrespective of TP53 mutation status. Br. J. Cancer, 72: 883-888, 1995.
27. Jacobs, I. J., Kohler, M. F., Wiseman, R. W., Marks, J. R., Whitaker, R., Kerns, B. A., Humphrey, P., Berchuck, A., Ponder, B. A., and Bast, R. C., Jr. Clonal origin of epithelial ovarian carcinoma, analysis by loss of heterozygosity, p53 mutation, and X-chromosome inactivation. J. Natl. Cancer Inst., 84: 1793-1798, 1992.
28. Enomoto, T., Fujita, M., Inoue, M., Tanizawa, O., Nomura, T., and Shroyer, K. R. Analysis of clonality by amplification of short tandem repeats: carcinomas of the female reproductive tract. Diagnostic Mol. Pathol., 3: 292-297, 1994.
29. Endo, Y., Sugimura, H., Kino, I. Monoclonality of normal human colonic crypts. Pathol. Int., 45: 602-604, 1995.
30. Hashimoto, K., Azuma, C., Kimura, T., Nobunaga, T., Kanai, T., Sawada, M., Noguchi, S., Saji, F. Clonal determination of uterine leiomyomas by analyzing differential inactivation of the X-chromosome-linked phosphoglycerokinase gene. Gynecol. Obstet. Invest., 40: 204-208, 1995.
31. Campbell, I. G., Beynon, G., Davis, M., and Englefield, P. LOH and mutation analysis of CDKN2 in primary human ovarian cancers. Int. J. Cancer, 63: 222-225, 1995.
32. Orphanos, V., McGown, G., Hey, Y., Thorncroft, M., Santibanezkoref, M., Russell, S. E. H., Hickey, I., Atkinson, R. J., and Boyle, J. M. Allelic imbalance of chromosome 6q in ovarian tumors. Br. J. Cancer, 71: 666-669, 1995.
33. Collins et al. A high density YAC contig map of human chromosome 22. Nature (Lond.), 377: 367-379, 1995.
34. 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.
35. Anderson, L. A., Friedman, L., Osborne-Lawrence, S., Lynch, E., Weissenbach, J., Bowcock, A., King, M. High-density genetic map of the BRCA1 region of chromosome 17q12-21. Genomics, 17: 618-632, 1993.
36. Gyapay, G., Morissette, J., Vignal, A., Dib, C., Fizames, C., Millasseau, P., Marc, S., Bernardi, G., Lathrop, M., and Weissenbach, J. The 1993-94 Genethon human genetic linkage map. Nat. Genet., 7: 246-339, 1994.