The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Trends Cancer. 2021 Dec;7(12):1102-1118. doi: 10.1016/j.trecan.2021.08.007. Epub 2021 Sep 22.
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.
同源重组缺陷(HRD)肿瘤,包括那些携带有 BRCA 基因突变的肿瘤,对聚(ADP-核糖)聚合酶(PARP)抑制剂的治疗高度敏感。尽管有很高的缓解率,但大多数 HRD 癌症最终通过回复突变或 DNA 修复途径的遗传/表观遗传改变对 PARPi 治疗产生耐药性。因此,对抗这些耐药途径,从而提高 PARPi 治疗的效力,代表了一种提高 HRD 癌症治疗效果的潜在策略。在这篇综述中,我们讨论了最近从遗传筛选中获得的一些新见解,这些见解确定了一些可以靶向的新基因,以改善 HRD 癌症的 PARPi 治疗,并可能提供克服 PARPi 耐药的方法。