奥拉帕尼
基因敲除
癌症研究
生物
三阴性乳腺癌
同源重组
乳腺癌
PARP1
PARP抑制剂
分子生物学
小发夹RNA
癌症
细胞凋亡
聚ADP核糖聚合酶
聚合酶
DNA
遗传学
作者
Xin Peng,Yingying Wang,Zixiang Yu,Shengfan Huang,Shaolu Zhang,Zhenxing Zhong,Yongzhe Wang,Shanshan Liu,Kailin Wang,Christophe Nicot,François X. Claret,Dexin Kong
标识
DOI:10.1186/s12943-025-02422-7
摘要
This study uncovers a novel role for Jab1 as an RBP, specifically through interactions between its MPN domain and HRR-related RNAs, regulating RNA stability and maintaining HRR competency. Targeting Jab1 represents a promising strategy to pharmacologically induce HRD and enhance the efficacy of PARPi therapies in TNBC. This combination approach may hold translational value for improving clinical outcomes in patients with TNBC.
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