BRCA1 in breast and ovarian cancer predisposition

被引:17
作者
Billack, B
Monteiro, ANA
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL 33612 USA
[2] St Johns Univ, Dept Pharmaceut Sci, Coll Pharm & Allied Hlth Profess, Jamaica, NY 11439 USA
关键词
BRCA1; breast cancer; DNA damage; ubiquitination; BRCT domain;
D O I
10.1016/j.canlet.2004.11.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Women carrying one mutated BRCA1 allele are at increased risk of developing breast and ovarian cancer but tumor initiation requires the loss of the wild-type allele indicating that it is a tumor suppressor gene. In the 10 years since the cloning of BRCA1, a function for the gene product in the DNA damage response has been established. However, identifying the exact biochemical activities of BRCA1 has been a more difficult task. Our current understanding suggests that the molecular functions mediated by the terminal ends of BRCA1, which include an E3 ubiquitin ligase activity at the N-terminus and a protein-protein interaction surface at the C-terminus, are critical to the function of this protein in the response to DNA damage. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1 / 7
页数:7
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