车站3
药物重新定位
STAT蛋白
抗药性
癌症研究
癌变
机制(生物学)
癌症
细胞生物学
生物
药理学
药品
医学
信号转导
生物信息学
内科学
遗传学
哲学
认识论
作者
Chengguang Zhao,Huameng Li,Huey‐Jen Lin,Shulin Yang,Jiayuh Lin,Guang Liang
标识
DOI:10.1016/j.tips.2015.10.001
摘要
Signal transducer and activator of transcription 3 (STAT3) plays crucial roles in several cellular processes such as cell proliferation and survival, and has been found to be aberrantly activated in many cancers. Much research has explored the leading mechanisms for regulating the STAT3 pathway and its role in promoting tumorigenesis. We focus here on recent evidence suggesting that feedback activation of STAT3 plays a prominent role in mediating drug resistance to a broad spectrum of targeted cancer therapies and chemotherapies. We highlight the potential of co-targeting STAT3 and its primary target to overcome drug resistance, and provide perspective on repurposing clinically approved drugs as STAT3 pathway inhibitors, in combination with the FDA-approved receptor tyrosine kinase (RTK) inhibitors, to improve clinical outcome of cancer treatment.
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