Feedback Activation of STAT3 as a Cancer Drug-Resistance Mechanism

被引:203
|
作者
Zhao, Chengguang [1 ,2 ,3 ]
Li, Huameng [3 ]
Lin, Huey-Jen [4 ]
Yang, Shulin [1 ]
Lin, Jiayuh [2 ]
Liang, Guang [3 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Environm & Biol Engn, Nanjing 210094, Jiangsu, Peoples R China
[2] Ohio State Univ, Nationwide Childrens Hosp, Ctr Childhood Canc & Blood Dis,Res Inst, Dept Pediat,Coll Med, Columbus, OH 43205 USA
[3] Wenzhou Med Univ, Sch Pharmaceut Sci, Chem Biol Res Ctr, Wenzhou 325035, Zhejiang, Peoples R China
[4] Univ Delaware, Dept Med Lab Sci, Newark, DE 19716 USA
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
GROWTH-SUPPRESSIVE ACTIVITY; TRANSCRIPTION; 3; STAT3; DNA-BINDING ACTIVITY; SMALL-MOLECULE INHIBITOR; MULTIPLE-MYELOMA CELLS; HUMAN OVARIAN-CANCER; SIGNAL TRANSDUCER; BREAST-CANCER; HEPATOCELLULAR-CARCINOMA; ANTITUMOR-ACTIVITY;
D O I
10.1016/j.tips.2015.10.001
中图分类号
R9 [药学];
学科分类号
1007 ;
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.
引用
收藏
页码:47 / 61
页数:15
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