软膜
奥拉帕尼
聚ADP核糖聚合酶
PARP抑制剂
DNA损伤修复
化学
癌症研究
乳腺癌
聚合酶
合成致死
癌症
DNA修复
医学
DNA
生物化学
内科学
作者
Ling Yu,Yan Zhou,Youde Wang,Miao Hao,Jingyi Zhao,Chong Peng,Shuai Li
标识
DOI:10.1007/s00044-022-02919-6
摘要
Poly (ADP-ribose) Polymerase-1 (PARP-1) is a member of 17 membered PARP family having diversified biological functions such as synthetic lethality, DNA repair, apoptosis, necrosis and histone binding, etc. The U.S. FDA has approved four PARP-1 inhibitors, namely Olaparib, Rucaparib, Niraparib, and Talazoparib. And, Veliparib has entered the late stage of clinical research as a PARP-1 inhibitor. At present, PARP-1 inhibitors have been approved for ovarian cancer, breast cancer, pancreatic cancer and other related indications. In recent years, more and more novel PARP-1 inhibitors have been reported. This review has attempted to summarize the structural types and characteristics of various novel PARP-1 inhibitors reported since 2020. And we outlined the current clinical application potential of PARP-1 inhibitors and further analyzed its current challenges and future development trends. Graphical abstract
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