The promising PARP inhibitors in ovarian cancer therapy: From Olaparib to others

被引:31
|
作者
Chen, Ying [1 ,2 ,3 ]
Du, Hui [4 ]
机构
[1] Tianjin Med Univ, Canc Inst & Hosp, Dept Gynecol Oncol, Tianjin 300060, Peoples R China
[2] Key Lab Canc Prevent & Therapy, Tianjin 300060, Peoples R China
[3] Natl Clin Res Ctr Canc, Tianjin 300060, Peoples R China
[4] Hebei Med Univ, Hosp 2, Dept Obstet & Gynecol, Shijiazhuang 050000, Hebei, Peoples R China
关键词
Epithelial ovarian cancer; PARP inhibitor; Olaparib; Veliparib; Rucaparib; Niraparib; PLATINUM-SENSITIVE OVARIAN; NEGATIVE BREAST-CANCER; HUMAN POLY(ADP-RIBOSE) POLYMERASE-1; PEGYLATED LIPOSOMAL DOXORUBICIN; GRADE SEROUS OVARIAN; MAINTENANCE THERAPY; SYNTHETIC LETHALITY; PRIMARY PERITONEAL; FALLOPIAN-TUBE; OPEN-LABEL;
D O I
10.1016/j.biopha.2018.01.094
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
Epithelial ovarian cancer (EOC) accounts for 90% of all ovarian cancer. Initially, approaching 80% of EOC patients respond to standard therapeutic strategy, cytoreduction combining with postoperative auxiliary platinum-based chemotherapy. However, relapse is approximately inevitable because of drug-resistance for high-grade serous ovarian cancer (HGSOC). Recently, the nuclear enzyme poly (ADP-ribose) polymerase (PARP) represents a strikingly novel target in EOC treatment. PARP inhibitors, currently mainly including Olaparib, Niraparib, Velaparib, Rucaparib, and Talazoparib, have demonstrated promising activity in EOC treatment. Especially, studies of Olaparib accelerated it to be approved in Europe and USA. Here, this review focuses on the pre-clinical data, current clinical trials, the development of PARP inhibitors in the last decade and their future roles in clinical treatment for EOC patients.
引用
收藏
页码:552 / 560
页数:9
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