Synthetic Lethality and Cancer Therapy: Lessons Learned from the Development of PARP Inhibitors

被引:371
作者
Lord, Christopher J. [1 ]
Tutt, Andrew N. J. [1 ,2 ]
Ashworth, Alan [1 ]
机构
[1] Inst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, England
[2] Kings Coll London, Breakthrough Breast Canc Res Unit, London WC2R 2LS, England
来源
ANNUAL REVIEW OF MEDICINE, VOL 66 | 2015年 / 66卷
基金
英国惠康基金;
关键词
BRCA1; BRCA2; drug resistance; breast cancer; ovarian cancer; DNA-DAMAGE RESPONSE; NEGATIVE BREAST-CANCER; BRCA MUTANT-CELLS; POLY(ADP-RIBOSE) POLYMERASE; HOMOLOGOUS RECOMBINATION; CISPLATIN RESISTANCE; SECONDARY MUTATIONS; REPAIR DEFECT; NUCLEAR PTEN; TUMOR-CELLS;
D O I
10.1146/annurev-med-050913-022545
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
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.
引用
收藏
页码:455 / 470
页数:16
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