Cargando…
Targeting HR Repair as a Synthetic Lethal Approach to Increase DNA Damage Sensitivity by a RAD52 Inhibitor in BRCA2-Deficient Cancer Cells
BRCA mutation, one of the most common types of mutations in breast and ovarian cancer, has been suggested to be synthetically lethal with depletion of RAD52. Pharmacologically inhibiting RAD52 specifically eradicates BRCA-deficient cancer cells. In this study, we demonstrated that curcumin, a plant...
Autores principales: | Tseng, Wei-Che, Chen, Chi-Yuan, Chern, Ching-Yuh, Wang, Chu-An, Lee, Wen-Chih, Chi, Ying-Chih, Cheng, Shu-Fang, Kuo, Yi-Tsen, Chiu, Ya-Chen, Tseng, Shih-Ting, Lin, Pei-Ya, Liou, Shou-Jhen, Li, Yi-Chen, Chen, Chin-Chuan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122931/ https://www.ncbi.nlm.nih.gov/pubmed/33922657 http://dx.doi.org/10.3390/ijms22094422 |
Ejemplares similares
-
RAD52: Paradigm of Synthetic Lethality and New Developments
por: Rossi, Matthew J., et al.
Publicado: (2021) -
Identification of a RAD52 Inhibitor Inducing Synthetic Lethality in BRCA2-Deficient Cancer Cells
por: Yang, Qianye, et al.
Publicado: (2021) -
Simultaneous Targeting of PARP1 and RAD52 Triggers Dual Synthetic Lethality in BRCA-Deficient Tumor Cells
por: Sullivan-Reed, Katherine, et al.
Publicado: (2018) -
The endonuclease EEPD1 mediates synthetic lethality in RAD52-depleted BRCA1 mutant breast cancer cells
por: Hromas, Robert, et al.
Publicado: (2017) -
RAD52 as a Potential Target for Synthetic Lethality-Based Anticancer Therapies
por: Toma, Monika, et al.
Publicado: (2019)