同源重组
生物
DNA修复
突变
表观遗传学
基因
癌症研究
复归
聚合酶
PARP抑制剂
遗传学
聚ADP核糖聚合酶
抗药性
合成致死
表型
作者
Kasper Fugger,Graeme Hewitt,Stephen C. West,Simon J. Boulton
标识
DOI:10.1016/j.trecan.2021.08.007
摘要
Homologous recombination–deficient (HRD) tumours, including those harbouring mutations in the BRCA genes, are hypersensitive to treatment with inhibitors of poly(ADP-ribose) polymerase (PARPis). Despite high response rates, most HRD cancers ultimately develop resistance to PARPi treatment through reversion mutations or genetic/epigenetic alterations to DNA repair pathways. Counteracting these resistance pathways, thereby increasing the potency of PARPi therapy, represents a potential strategy to improve the treatment of HRD cancers. In this review, we discuss recent insights derived from genetic screens that have identified a number of novel genes that can be targeted to improve PARPi treatment of HRD cancers and may provide a means to overcome PARPi resistance.
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