奥拉帕尼
聚ADP核糖聚合酶
DNA修复
PARP抑制剂
同源重组
化学
癌症研究
合成致死
癌症治疗
聚合酶
癌症
DNA损伤
计算生物学
药理学
酶
DNA
生物
生物化学
遗传学
作者
Ying-Qing Wang,Pingyuan Wang,Yu-Ting Wang,Guang‐Fu Yang,Ao Zhang,Ze-Hong Miao
标识
DOI:10.1021/acs.jmedchem.6b00055
摘要
Poly(ADP-ribose)polymerase-1 (PARP-1) is a critical DNA repair enzyme in the base excision repair pathway. Inhibitors of this enzyme comprise a new type of anticancer drug that selectively kills cancer cells by targeting homologous recombination repair defects. Since 2010, important advances have been achieved in PARP-1 inhibitors. Specifically, the approval of olaparib in 2014 for the treatment of ovarian cancer with BRCA mutations validated PARP-1 as an anticancer target and established its clinical importance in cancer therapy. Here, we provide an update on PARP-1 inhibitors, focusing on breakthroughs in their clinical applications and investigations into relevant mechanisms of action, biomarkers, and drug resistance. We also provide an update on the design strategies and the structural types of PARP-1 inhibitors. Opportunities and challenges in PARP-1 inhibitors for cancer therapy will be discussed based on the above advances.
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