聚ADP核糖聚合酶
PARP抑制剂
PARP1
生物
合成致死
聚合酶
同源重组
机制(生物学)
奥拉帕尼
癌症研究
DNA修复
癌症
遗传学
DNA
认识论
哲学
出处
期刊:DNA Repair
[Elsevier]
日期:2018-11-01
卷期号:71: 172-176
被引量:328
标识
DOI:10.1016/j.dnarep.2018.08.021
摘要
BRCA1 and BRCA2 deficient tumor cells are sensitive to inhibitors of Poly ADP Ribose Polymerase (PARP1) through the mechanism of synthetic lethality. Several PARP inhibitors, which are oral drugs and generally well tolerated, have now received FDA approval for various ovarian cancer and breast cancer indications. Despite their use in the clinic, PARP inhibitor resistance is common and develops through multiple mechanisms. Broadly speaking, BRCA1/2-deficient tumor cells can become resistant to PARP inhibitors by restoring homologous recombination (HR) repair and/or by stabilizing their replication forks. Here, we review the mechanism of PARP inhibitor resistance.
科研通智能强力驱动
Strongly Powered by AbleSci AI