Male breast cancer in the hereditary nonpolyposis colorectal cancer syndrome

Breast Cancer Research and Treatment

Volumn 53, Issue 1, 1999, Pages 87-91

  Boyd, Jeff ^a   Rhei, Esther ^a   Federici, Mark G ^a   Borgen, Patrick I ^a   Watson, Patrice ^b   Franklin, Barbara ^b   Karr, Beth ^b   Lynch, Jane ^b   Lemon, Stephen J ^b   Lynch, Henry T ^b  

^a MEMORIAL SLOAN KETTERING CANCER CENTER   (United States)

^b CREIGHTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Hereditary; HNPCC; Male breast cancer; Microsatellite instability; Mismatch repair; MLH1

Indexed keywords

MICROSATELLITE DNA;

AGED; ARTICLE; BREAST CANCER; CASE REPORT; COLORECTAL CANCER; GENE MUTATION; GENE SEGREGATION; GERM LINE; HOMOZYGOSITY; HUMAN; HUMAN TISSUE; MALE; MALE BREAST; MICROSATELLITE INSTABILITY; PRIORITY JOURNAL;

AGED; ALLELES; BREAST NEOPLASMS, MALE; CARCINOMA, DUCTAL, BREAST; COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; DNA PRIMERS; GERM-LINE MUTATION; HUMANS; LOSS OF HETEROZYGOSITY; MALE; MICROSATELLITE REPEATS; PEDIGREE; POLYMERASE CHAIN REACTION;

EID: 0032974544     PISSN: 01676806     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1006030116357     Document Type: Article

References (25)

1. Miller BA, Ries LAG, Hankey BF, Kosary CL, Harras A, Devesa SS, Edwards BK: SEER Cancer Statistics Review: 1973-1990 (NIH Pub. No. 93-2789). National Cancer Institute, Bethesda, 1993
2. Borgen PI, Senie RT, McKinnon WMP, Rosen PP: Carcinoma of the male breast: Analysis and prognosis compared with matched female patients. Ann Surg Oncol 4: 385-388, 1997
3. Sasco AJ, Lowenfels AB, Pasker-de Jong P: Review article: epidemiology of male breast cancer. A meta-analysis of published case-control studies and discussion of selected aetiological factors. Int J Cancer 53: 538-549, 1993
4. Olsson H, Andersson H, Johansson O, Moller TR, Kristoffersson U, Wenngren E: Population-based cohort investigations of the risk for malignant tumors in first-degree relatives and wives of men with breast cancer. Cancer 71: 1273-1278, 1993
5. Rosenblatt KA, Thomas DB, McTiernan A, Austin MA, Stalsberg H, Stemhagen A, Thompson WD, Curnen MG, Sataraino W, Austin DF: Breast cancer in men: Aspects of familial aggregation. J Natl Cancer Inst 83: 849-854, 1991
6. Couch FJ, Farid LM, DeShano ML, Tavtigian SV, Calzone K, Campeau L, Peng Y, Bogden B, Chen Q, Neuhausen S, Shattuck-Eidens D, Godwin AK, Daly M, Radford DM, Sedlacek S, Rommens J, Simard J, Garber J, Merajver S, Weber BL: BRCA2 germline mutations in male breast cancer cases and breast cancer families. Nature Genet 13: 123-125, 1996
7. Friedman LS, Gayther SA, Kurosaki T, Gordon D, Noble B, Casey G, Ponder BAJ, Anton-Culver H: Mutation analysis of BRCA1 and BRCA2 in a male breast cancer population. Am J Hum Genet 60: 313-319, 1997
8. Struewing JP, Brody LC, Erdos MR, Kase RG, Giambarresi TR, Smith SA, Collins FS, Tucker MA: Detection of eight BRCA1 mutations in 10 breast/ovarian cancer families, including 1 family with male breast cancer. Am J Hum Genet 57: 1-7, 1995
9. Wooster R, Mangion J, Eeles R, Smith S, Dowsett M, Averill D, Barrett-Lee P, Easton DF, Ponder BAJ, Stratton MR: A germline mutation in the androgen receptor gene in two brothers with breast cancer and Reifenstein syndrome. Nature Genet 2: 132-134, 1992
10. Lobaccaro J-M, Lumbroso S, Belon C, Galtier-Dereure F, Bringer J, Lesimple T, Heron J-F, Pujol H, Sultan C: Male breast cancer and the androgen receptor gene. Nature Genet 5: 109-110, 1993
11. Lynch HT, Smyrk TC, Watson P, Lanspa SJ, Lynch PM, Cavalieri RJ, Boland CR: Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer. Gastroenterology 104: 1535-1549, 1993
12. Marra G, Boland CR: Hereditary nonpolyposis colorectal cancer: the syndrome, the genes, and historical perspectives. J Natl Cancer Inst 87: 1114-1125, 1995
13. Vasen HFA, Offerhaus GJA, den Hartog Jager FCA, Menko FH, Nagengast FM, Griffioen G, van Hogezand RB, Heintz APM: The tumour spectrum in hereditary non-polyposis colorectal cancer: a study of 24 kindreds in the Netherlands. Int J Cancer 46: 31-34, 1990
14. Mecklin J-P, Jarvinen HJ: Tumor spectrum in cancer family syndrome (hereditary nonpolyposis colorectal cancer). Cancer 68: 1109-1112, 1991
15. Watson P, Lynch HT: Extracolonic cancer in hereditary nonpolyposis colorectal cancer. Cancer 71: 677-685, 1993
16. Itoh H, Houlston RS, Harocopos C, Slack J: Risk of cancer death in first-degree relatives of patients with hereditary non-polyposis cancer syndrome (Lynch type II): a study of 130 kindreds in the United Kingdom. Br J Surg 77: 1367-1370, 1990
17. Nelson CL, Sellers TA, Rich SS, Potter JD, McGovern PG, Kushi LH: Familial clustering of colon, breast, uterine, and ovarian cancers as assessed by family history. Genet Epidemiol 10: 235-244, 1993
18. Risinger JI, Barrett JC, Watson P, Lynch HT, Boyd J: Molecular genetic evidence of the occurrence of breast cancer as an integral tumor in the hereditary nonpolyposis colorectal carcinoma syndrome. Cancer 77: 1836-1843, 1996
19. Fishel R, Kolodner R: Identification of mismatch repair genes and their role in the development of cancer. Curr Opin Genet Dev 5: 382-395, 1995
20. Boyd J, Takahashi H, Waggoner SE, Jones LA, Hajek RA, Wharton JT, Liu F-S, Fujino T, Barrett JC, McLachlan JA: Molecular genetic analysis of clear cell adenocarcinomas of the vagina and cervix associated and unassociated with diethylstilbestrol exposure in utero. Cancer 77: 507-513, 1995
21. Parsons R, Myeroff L, Liu B, Willson JKV, Markowitz S, Kinzler KW, Vogelstein B: Microsatellite instability and mutations of the transforming growth factor β type II receptor gene in colorectal cancer. Cancer Res 55: 5548-5550, 1995
22. Lynch HT, Bronson EK, Strayhorn PC, Smyrk TC, Lynch JF, Ploetner EJ: Genetic diagnosis of Lynch syndrome II in an extended colorectal cancer-prone family. Cancer 66: 2233-2238, 1990
23. Hoang J-M, Cottu PH, Thuille B, Salmon RJ, Thomas G, Hamelin R: BAT-26, an indicator of the replication error phenotype in colorectal cancers and cell lines. Cancer Res 57: 300-303, 1997
24. Papadopoulos N, Nicolaides NC, Wei Y-F, Ruben SM, Carter KC, Rosen CA, Haseltine WA, Fleischmann RD, Fraser CM, Adams MD, Venter JC, Hamilton SR, Petersen GM, Watson P, Lynch HT, Peltomäki P, Mecklin J-P, de la Chapelle A, Kinzler KW, Vogelstein B: Mutation of a mutL homolog in hereditary colon cancer. Science 263: 1625-1629, 1994
25. Hackman P, Tannergård P, Osei-Mensa S, Chen J, Kane MF, Kolodner R, Lambert B, Hellgren D, Lindblom A: A human compound heterozygote for two MLH1 missense mutations. Nature Genet 17: 135-136, 1997