Abstract
Germline mutations of BRCA1 confer hereditary susceptibility to breast and ovarian cancer. However, somatic mutation of BRCA1 is infrequent in sporadic breast cancers. The BRCA1 protein C terminus (BRCT) domains interact with multiple proteins and are required for BRCA1's tumor-suppressor function. In this study,wedemonstratedthat Abraxas, aBRCA1 BRCT domain-interacting protein, plays a role in tumor suppression. Abraxas exerts its function through binding toBRCA1 to regulateDNArepair and maintain genome stability. Both homozygous and heterozygous Abraxas knockout mice exhibited decreased survival and increased tumor incidence. The gene encoding Abraxas suffers from gene copy loss and somatic mutations in multiple human cancers including breast, ovarian, and endometrial cancers, suggesting that mutation and loss of function of Abraxas may contribute to tumor development in human patients.
Original language | English (US) |
---|---|
Pages (from-to) | 807-817 |
Number of pages | 11 |
Journal | Cell Reports |
Volume | 8 |
Issue number | 3 |
DOIs | |
State | Published - Aug 7 2014 |
ASJC Scopus subject areas
- General Biochemistry, Genetics and Molecular Biology
MD Anderson CCSG core facilities
- Genetically Engineered Mouse Facility
- Research Animal Support Facility