Mechanisms of BRCA1 Tumor Suppression
Open accessAbstract
The p220 BRCA1 tumor suppressor protein has been implicated in multiple biochemical and biologic functions since its molecular cloning 18 years ago. Here, we discuss those functions most relevant for its tumor-suppressing activities with an emphasis on new findings. In particular, this review focuses on what is known of the activities of those BRCA1-binding partners that have tumor suppressor functions, on the reversion of mutant BRCA1 alleles concomitant with therapy resistance, on insights gained from studies of BRCA1 structure–function relationships, recent findings from animal models, and the potential role of BRCA1 in some nonhereditary tumors. From this information, a more detailed and refined picture of BRCA1 tumor suppression is beginning to emerge. Although key mysteries remain—such as why BRCA1 tumor suppression is focused on carcinomas of the breast and ovary—the pace of discovery is increasing. Significance: BRCA1 functions as a clinically important classical tumor suppressor in hereditary breast and ovarian cancer; here, we review progress in understanding how BRCA1 operates to suppress tumor formation. Cancer Discov; 2(8); 679–84. ©2012 AACR.
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The BRCA1-BARD1 complex acts in homologous recombination-mediated repair of DNA double-strand breaks.
“The tumor suppressor complex BRCA1-BARD1 functions in DNA double-strand break repair by homologous recombination.”
From BRCA1–BARD1 promotes RAD51-mediated homologous DNA pairing (2017) · cites this paper as [3]
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References 52 · Cited by 159
Research works printed but not linked: 1
- [29]ter Brugge P van der Burg E Kristel P Boon U Moutinho Freixas C Esteller M Response and Acquired Resistance of BRCA1-Deficient Triple-Negative Breast Cancer Xenografts to Alkylators or PARP Inhibitors San Antonio Breast Cancer Symposium 2011
- Authors
- Silver, D. P., & Livingston, D. M.
- Affiliations
- Dana-Farber Cancer Institute (US)
- Corresponding author
- Livingston, David M.
- Venue
- Cancer Discovery
- Published
- 2012-08-01
- Volume
- 2
- Issue
- 8
- Pages
- 679-684
- ISSN
- 2159-8274 (ISSN-L)
- 2159-8290
- PMC
- PMC3437262
- OpenAlex
- W2156001194
- Cited by
- 159
- References
- 52
- Citations by year
- 2026: 4 · 2025: 7 · 2024: 7 · 2023: 7 · 2022: 18 · 2021: 11 · 2020: 17 · 2019: 16 · 2018: 11 · 2017: 9 · 2016: 9 · 2015: 11 · 2014: 18 · 2013: 13 · 2012: 1
- FWCI
- 1.68
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Cancer Discovery (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Cancer Institute (K08CA082572, CA 089393, R01CA136512, P01CA080111, P50CA089393)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › BRCA gene mutations in cancer
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Keywords
- BRCA1, tumor suppression, treatment resistance, structure-function relationship, hereditary breast cancer, hereditary ovarian cancer, animal models
- MeSH terms
- Animals, Breast Neoplasms, Female, Humans, Mutation, Ovarian Neoplasms, BRCA1 Protein, Genes, BRCA1
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