The development of PARP inhibitors in ovarian cancer: from bench to bedside

被引:40
作者
Drew, Yvette [1 ,2 ]
机构
[1] Newcastle Univ, Northern Inst Canc Res, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[2] Freeman Rd Hosp, Northern Ctr Canc Care, Newcastle Upon Tyne, Tyne & Wear, England
关键词
olaparib; PARP; ovarian cancer; STRAND BREAK REPAIR; POLY(ADP-RIBOSE) POLYMERASE INHIBITORS; SUSCEPTIBILITY GENE BRCA1; RANDOMIZED PHASE-2 TRIAL; HOMOLOGOUS RECOMBINATION; MUTATION CARRIERS; DNA; CELLS; THERAPY; MAINTENANCE;
D O I
10.1038/bjc.2015.394
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The nuclear enzyme poly (ADP-ribose) polymerase (PARP) represents an important novel target in the treatment of ovarian cancer. This article charts over 50 years of research from the discovery of the first PARP enzyme in 1963, to the approval and licensing in 2015 of the first PARP inhibitor, olaparib (Lynparza), in the treatment of BRCA-mutated ovarian cancer.
引用
收藏
页码:S3 / S9
页数:7
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