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Increasing DNA damage sensitivity through corylin-mediated inhibition of homologous recombination.
- Source :
-
Biomedicine & Pharmacotherapy . Jul2024, Vol. 176, pN.PAG-N.PAG. 1p. - Publication Year :
- 2024
-
Abstract
- DNA repair allows the survival of cancer cells. Therefore, the development of DNA repair inhibitors is a critical need for sensitizing cancers to chemoradiation. Sae2CtIP has specific functions in initiating DNA end resection, as well as coordinating cell cycle checkpoints, and it also greatly interacts with the DDR at different levels. In this study, we demonstrated that corylin, a potential sensitizer, causes deficiencies in DNA repair and DNA damage checkpoints in yeast cells. More specifically, corylin increases DNA damage sensitivity through the Sae2-dependent pathway and impairs the activation of Mec1-Ddc2, Rad53-p and γ-H2A. In breast cancer cells, corylin increases apoptosis and reduces proliferation following Dox treatment by inhibiting CtIP. Xenograft assays showed that treatment with corylin combined with Dox significantly reduced tumor growth in vivo. Our findings herein delineate the mechanisms of action of corylin in regulating DNA repair and indicate that corylin has potential long-term clinical utility as a DDR inhibitor. [Display omitted] • Corylin inhibits DNA repair and DNA damage checkpoints in the SSA system. • Corylin increases DNA damage sensitivity through the Sae2CtIP-dependent pathway. • The combination of corylin and Doxorubicin significantly suppressed tumor growth. [ABSTRACT FROM AUTHOR]
- Subjects :
- *HOMOLOGOUS recombination
*DNA damage
*DNA repair
*CELL cycle
*TUMOR growth
Subjects
Details
- Language :
- English
- ISSN :
- 07533322
- Volume :
- 176
- Database :
- Academic Search Index
- Journal :
- Biomedicine & Pharmacotherapy
- Publication Type :
- Academic Journal
- Accession number :
- 177909193
- Full Text :
- https://doi.org/10.1016/j.biopha.2024.116864