An Update on Poly(ADP-ribose)polymerase-1 (PARP-1) Inhibitors: Opportunities and Challenges in Cancer Therapy

被引:181
|
作者
Wang, Ying-Qing [1 ]
Wang, Ping-Yuan [2 ,3 ,4 ]
Wang, Yu-Ting [1 ]
Yang, Guang-Fu [4 ]
Zhang, Ao [2 ,3 ]
Miao, Ze-Hong [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Div Antitumor Pharmacol, Shanghai 201203, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Mat Med, CAS Key Lab Receptor Res, 555 Zuchongzhi Lu,Bldg 3,Room 426, Shanghai 201203, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Mat Med, Synthet Organ & Med Chem Lab, 555 Zuchongzhi Lu,Bldg 3,Room 426, Shanghai 201203, Peoples R China
[4] Cent China Normal Univ, Coll Chem, Key Lab Pesticide & Chem Biol, Minist Educ, Wuhan 430079, Peoples R China
基金
中国国家自然科学基金;
关键词
SEROUS OVARIAN-CANCER; OLAPARIB MAINTENANCE THERAPY; RIBOSE POLYMERASE INHIBITOR; CYCLIN-DEPENDENT KINASE-5; NEGATIVE BREAST-CANCER; PHASE-I TRIAL; DNA-REPAIR; HOMOLOGOUS-RECOMBINATION; BIOLOGICAL EVALUATION; TUMOR-CELLS;
D O I
10.1021/acs.jmedchem.6b00055
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Poly(ADP-ribose)polymerase-1 (PARP-1) is a critical DNA repair enzyme in the base excision repair pathway. Inhibitors of this enzyme comprise a new type of anticancer drug that selectively kills cancer cells by targeting, homologous recombination repair defects. Since 2010, important advances have been achieved in PARP-1 inhibitors. Specifically, the approval of olaparib in 2014 for the treatment of ovarian cancer with BRCA mutations validated PARP-1 as an anticancer target and established its clinical importance in cancer therapy. Here, we provide an update on PARP-1 inhibitors, focusing on breakthroughs in their clinical applications and investigations into relevant mechanisms of action, biomarkers, and drug resistance. We also provide an update on the design strategies and the structural types of PARP-1 inhibitors. Opportunities and challenges in PARP-1 inhibitors for cancer therapy will be discussed based on, the above advances.
引用
收藏
页码:9575 / 9598
页数:24
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