体内
体外
癌症
Ku70型
癌症研究
DNA损伤
DNA
生物
遗传学
作者
Xuening Chen,C. H. Chen,Chenmei Luo,Jianyong Liu,Zhonghui Lin
标识
DOI:10.1016/j.ejphar.2024.176647
摘要
The emergence of chemoresistance poses a significant challenge to the efficacy of DNA-damaging agents in cancer treatment, in part due to the inherent DNA repair capabilities of cancer cells. The Ku70/80 protein complex (Ku) plays a central role in double-strand breaks (DSBs) repair through the classical non-homologous end joining (c-NHEJ) pathway, and has proven to be one of the most promising drug target for cancer treatment when combined with radiotherapy or chemotherapy. In this study, we conducted a high-throughput screening of small-molecule inhibitors targeting the Ku complex by using a fluorescence polarization-based DNA binding assay. From a library of 11,745 small molecules, UMI-77 was identified as a potent Ku inhibitor, with an IC
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