Tackling PARP inhibitor resistance

被引:27
|
作者
Fugger, Kasper [1 ]
Hewitt, Graeme [1 ]
West, Stephen C. [1 ]
Boulton, Simon J. [1 ,2 ]
机构
[1] Francis Crick Inst, 1 Midland Rd, London NW1 1AT, England
[2] Artios Pharma Ltd, B940,Babraham Res Campus, Cambridge CB22 3FH, England
来源
TRENDS IN CANCER | 2021年 / 7卷 / 12期
基金
欧盟地平线“2020”;
关键词
BASE EXCISION-REPAIR; DNA-POLYMERASE BETA; HOMOLOGOUS-RECOMBINATION; POLY(ADP-RIBOSE) POLYMERASE; SYNTHETIC LETHALITY; ADP-RIBOSYLATION; CANCER; ENZYME; THETA; GENE;
D O I
10.1016/j.trecan.2021.08.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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.
引用
收藏
页码:1102 / 1118
页数:17
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