Cancer risks for male carriers of germline mutations in BRCA1 or BRCA2: A review of the literature

被引:291
作者
Liede, A
Karlan, BY
Narod, SA
机构
[1] Cedars Sinai Med Ctr, Womens Canc Res Inst, Los Angeles, CA 90048 USA
[2] Sunnybrook & Womens Coll Hlth Sci Ctr, Ctr Res Womens Hlth, Toronto, ON, Canada
关键词
D O I
10.1200/JCO.2004.05.055
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Major risks conferred by BRCA1 and BRCA2 in women are for cancers of the breast, ovary, fallopian tube, and peritoneum. Male carriers of mutations in BRCA1 or BRCA2 are also susceptible to cancer; however, their risks remain poorly understood and their optimal clinical management has not. yet been defined. This article reviews studies that estimate risk associated with mutations in BRCA1 or BRCA2 with a focus on the cancer sites most relevant to men. Male BRCA1 mutation carriers are at increased risk of cancers of the prostate and breast. Evidence supporting increased susceptibility to colon cancer is limited. In contrast to women, who have a greater lifetime risk of cancer with mutations of the BRCA1 gene, BRCA2 is the more important gene for men. The spectrum of cancers is wide for BRCA2 and some studies report that the overall cancer risk for male BRCA2 carriers exceeds the risk for female carriers. In particular, the relative risk to male BRCA2 mutation carriers is high before age 65 years, largely attributable to breast, prostate, and pancreatic cancers. BRCA2 mutation carriers are also at risk of stomach cancer and melanoma (of the skin and eye). Additional research into risks to male BRCA1 or BRCA2 mutation carriers is necessary, specifically to determine the magnitude of excess cancer risk among BRCA2 carriers and to increase our understanding of the basis for the observed site-specificity in cancer development. (C) 2004 by American Society of Clinical Oncology.
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页码:735 / 742
页数:8
相关论文
共 74 条
[1]  
BASHAM VM, 2002, HUM MUTAT, V4, pR2
[2]  
Berman DB, 1996, CANCER RES, V56, P3409
[3]   The BRC repeats are conserved in mammalian BRCA2 proteins [J].
Bignell, G ;
Micklem, G ;
Stratton, MR ;
Ashworth, A ;
Wooster, R .
HUMAN MOLECULAR GENETICS, 1997, 6 (01) :53-58
[4]  
Breast Canc Linkage Consortium, 1999, JNCI-J NATL CANCER I, V91, P1310
[5]  
Breslow NE, 1987, STAT METHODS CANC RE, VII
[6]  
Brose MS, 2002, J NATL CANCER I, V94, P1365, DOI 10.1093/jnci/94.18.1365
[7]   Recommendations for follow-up care of individuals with an inherited predisposition to cancer .2. BRCA1 and BRCA2 [J].
Burke, W ;
Daly, M ;
Garber, J ;
Botkin, J ;
Kahn, MJE ;
Lynch, P ;
McTierman, A ;
Offit, K ;
Perlman, J ;
Petersen, G ;
Thomson, E ;
Varricchio, C .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1997, 277 (12) :997-1003
[8]   The frequency of the predominant Jewish mutations in BRCA1 and BRCA2 in unselected Ashkenazi colorectal cancer patients [J].
Chen-Shtoyerman, R ;
Figer, A ;
Fidder, HH ;
Rath, P ;
Yeremin, L ;
Bar Meir, S ;
Friedman, E ;
Theodor, L .
BRITISH JOURNAL OF CANCER, 2001, 84 (04) :475-477
[9]   BRCA2 germline mutations in male breast cancer cases and breast cancer families [J].
Couch, FJ ;
Farid, LM ;
DeShano, ML ;
Tavtigian, SV ;
Calzone, K ;
Campeau, L ;
Peng, Y ;
Bogden, B ;
Chen, Q ;
Neuhausen, S ;
ShattuckEidens, D ;
Godwin, AK ;
Daly, M ;
Radford, DM ;
Sedlacek, S ;
Rommens, J ;
Simard, J ;
Garber, J ;
Merajver, S ;
Weber, BL .
NATURE GENETICS, 1996, 13 (01) :123-125
[10]  
Csokay B, 1999, CANCER RES, V59, P995