Research Progress of PARP Inhibitor Monotherapy and Combination Therapy for Endometrial Cancer

医学 同源重组 联合疗法 奥拉帕尼 PARP抑制剂 癌症研究 子宫内膜癌 肿瘤科 聚ADP核糖聚合酶 内科学 PI3K/AKT/mTOR通路 癌症 卵巢癌 聚合酶 生物 基因 信号转导 遗传学
作者
Ke Shen,Li Yang,Feiyan Li,Feng Zhang,Leilei Ding,Jing Yang,Jie Lu,Nannan Wang,Yan Wang
出处
期刊:Current Drug Targets [Bentham Science]
卷期号:23 (2): 145-155 被引量:27
标识
DOI:10.2174/1389450122666210617111304
摘要

: Endometrial cancer is one of the three most common malignant tumors in the female reproductive system. Advanced and recurrent endometrial cancers have poor prognoses and lack effective treatments. Poly (ADP-ribose) polymerase (PARP) inhibitors have been applied to many different types of tumors, and they can selectively kill tumor cells that are defective in homologous recombination repair. Endometrial cancer is characterized by mutations in homologous recombination repair genes; accordingly, PARP inhibitors have achieved positive results in off-label treatments of endometrial cancer cases. Clinical trials of PARP inhibitors as monotherapies and within combination therapies for endometrial cancer are ongoing. For this review, we searched PubMed with “endometrial cancer” and “PARP inhibitor” as keywords, and we used “olaparib”, “rucaparib”, “niraparib” and “talazoparib” as search terms in clinicaltrials.gov for ongoing trials. The literature search ended in October 2020, and only English-language publications were selected. Multiple studies confirm that PARP inhibitors play an important role in killing tumor cells with defects in homologous recombination repair. Its combination with immune checkpoint inhibitors, PI3K/AKT/mTOR pathway inhibitors, cell cycle checkpoint inhibitors, and other drugs can improve the treatment of endometrial cancer.
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