奥拉帕尼
PARP抑制剂
合成致死
聚ADP核糖聚合酶
聚合酶
癌症研究
DNA修复
生物
医学
药理学
基因
遗传学
作者
Amy Dréan,Christopher J. Lord,Alan Ashworth
标识
DOI:10.1016/j.critrevonc.2016.10.010
摘要
In 2014, olaparib (Lynparza) became the first PARP (Poly(ADP-ribose) polymerase) inhibitor to be approved for the treatment of cancer. When used as single agents, PARP inhibitors can selectively target tumour cells with BRCA1 or BRCA2 tumour suppressor gene mutations through synthetic lethality. However, PARP inhibition also shows considerable promise when used together with other therapeutic agents. Here, we summarise both the pre-clinical and clinical evidence for the utility of such combinations and discuss the future prospects and challenges for PARP inhibitor combinatorial therapies.
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