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Estrogen Induces RAD51C Expression and Localization to Sites of DNA Damage

Overview
Journal Cell Cycle
Specialty Cell Biology
Date 2016 Nov 5
PMID 27753535
Citations 7
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Abstract

Homologous recombination (HR) is a conserved process that maintains genome stability and cell survival by repairing DNA double-strand breaks (DSBs). The RAD51-related family of proteins is involved in repair of DSBs; consequently, deregulation of RAD51 causes chromosomal rearrangements and stimulates tumorigenesis. RAD51C has been identified as a potential tumor suppressor and a breast and ovarian cancer susceptibility gene. Recent studies have also implicated estrogen as a DNA-damaging agent that causes DSBs. We found that in ERα-positive breast cancer cells, estrogen transcriptionally regulates RAD51C expression in ERα-dependent mechanism. Moreover, estrogen induces RAD51C assembly into nuclear foci at DSBs, which is a precursor to RAD51 complex recruitment to the nucleus. Additionally, disruption of ERα signaling by either anti-estrogens or siRNA prevented estrogen induced upregulation of RAD51C. We have also found an association of a worse clinical outcome between RAD51C expression and ERα status of tumors. These findings provide insight into the mechanism of genomic instability in ERα-positive breast cancer and suggest that individuals with mutations in RAD51C that are exposed to estrogen would be more susceptible to accumulation of DNA damage, leading to cancer progression.

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References
1.
Vaz F, Hanenberg H, Schuster B, Barker K, Wiek C, Erven V . Mutation of the RAD51C gene in a Fanconi anemia-like disorder. Nat Genet. 2010; 42(5):406-9. DOI: 10.1038/ng.570. View

2.
Meindl A, Hellebrand H, Wiek C, Erven V, Wappenschmidt B, Niederacher D . Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene. Nat Genet. 2010; 42(5):410-4. DOI: 10.1038/ng.569. View

3.
Pittman D, Weinberg L, Schimenti J . Identification, characterization, and genetic mapping of Rad51d, a new mouse and human RAD51/RecA-related gene. Genomics. 1998; 49(1):103-11. DOI: 10.1006/geno.1998.5226. View

4.
Min A, Im S, Yoon Y, Song S, Nam H, Hur H . RAD51C-deficient cancer cells are highly sensitive to the PARP inhibitor olaparib. Mol Cancer Ther. 2013; 12(6):865-77. DOI: 10.1158/1535-7163.MCT-12-0950. View

5.
Yamnik R, Digilova A, Davis D, Brodt Z, Murphy C, Holz M . S6 kinase 1 regulates estrogen receptor alpha in control of breast cancer cell proliferation. J Biol Chem. 2008; 284(10):6361-9. DOI: 10.1074/jbc.M807532200. View