合成致死
杀伤力
聚ADP核糖聚合酶
PARP抑制剂
癌症
生殖系
DNA修复
突变
突变体
聚合酶
生物
基因
计算生物学
癌症研究
医学
遗传学
作者
Christopher J. Lord,Andrew Tutt,Alan Ashworth
标识
DOI:10.1146/annurev-med-050913-022545
摘要
The genetic concept of synthetic lethality, in which the combination or synthesis of mutations in multiple genes results in cell death, provides a framework to design novel therapeutic approaches to cancer. Already there are promising indications, from clinical trials exploiting this concept by using poly(ADP-ribose) polymerase (PARP) inhibitors in patients with germline BRCA1 or BRCA2 gene mutations, that this approach could be beneficial. We discuss the biological rationale for BRCA-PARP synthetic lethality, how the synthetic lethal approach is being assessed in the clinic, and how mechanisms of resistance are starting to be dissected. Applying the synthetic lethal concept to target non-BRCA-mutant cancers also has clear potential, and we discuss how some of the principles learned in developing PARP inhibitors might also drive the development of additional genetic approaches.
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