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
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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