Estrogen Induces RAD51C Expression and Localization to Sites of DNA Damage
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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.
Do Q, Tzeng S, Wang C, Wu C, Kafeenah H, Chen S Commun Biol. 2025; 8(1):357.
PMID: 40069327 PMC: 11897211. DOI: 10.1038/s42003-025-07657-0.
Lazzari G, Opattova A, Arena S J Exp Clin Cancer Res. 2024; 43(1):146.
PMID: 38750579 PMC: 11094891. DOI: 10.1186/s13046-024-03065-0.
Abe A, Imoto I, Ueki A, Nomura H, Kanao H Int J Mol Sci. 2022; 23(19).
PMID: 36233090 PMC: 9570179. DOI: 10.3390/ijms231911790.
The Interplay between the Cellular Response to DNA Double-Strand Breaks and Estrogen.
Yedidia-Aryeh L, Goldberg M Cells. 2022; 11(19).
PMID: 36231059 PMC: 9563627. DOI: 10.3390/cells11193097.
Fanconi anemia and mTOR pathways functionally interact during stalled replication fork recovery.
Nolan M, Knudson K, Holz M, Chaudhury I FEBS Lett. 2021; 595(5):595-603.
PMID: 33423298 PMC: 7993987. DOI: 10.1002/1873-3468.14035.