Recent Update on Development of Small-Molecule STAT3 Inhibitors for Cancer Therapy: From Phosphorylation Inhibition to Protein Degradation

被引:135
|
作者
Dong, Jinyun [1 ,2 ]
Cheng, Xiang-Dong [1 ,2 ]
Zhang, Wei-Dong [3 ]
Qin, Jiang-Jiang [1 ,2 ]
机构
[1] Univ Chinese Acad Sci, Canc Hosp, Zhejiang Canc Hosp, Hangzhou 310022, Zhejiang, Peoples R China
[2] Chinese Acad Sci, Inst Basic Med & Canc IBMC, Hangzhou 310018, Zhejiang, Peoples R China
[3] Naval Med Univ, Sch Pharm, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
TRANSCRIPTION; 3; STAT3; DNA-BINDING ACTIVITY; SIGNAL TRANSDUCER; INDOLEAMINE 2,3-DIOXYGENASE; TARGETING STAT3; BIOLOGICAL EVALUATION; TUMOR-GROWTH; IN-VITRO; DERIVATIVES; ACTIVATION;
D O I
10.1021/acs.jmedchem.1c00629
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Signal transducer and activator of transcription 3 (STAT3) is a transcription factor that regulates various biological processes, including proliferation, metastasis, angiogenesis, immune response, and chemoresistance. In normal cells, STAT3 is tightly regulated to maintain a transiently active state, while persistent STAT3 activation occurs frequently in cancers, associating with a poor prognosis and tumor progression. Targeting the STAT3 protein is a potentially promising therapeutic strategy for tumors. Although none of the STAT3 inhibitors has been marketed yet, a few of them have succeeded in entering clinical trials. This Review aims to systematically summarize the progress of the last 5 years in the discovery of directive STAT3 small-molecule inhibitors and degraders, focusing primarily on their structural features, design strategies, and bioactivities. We hope this Review will shed light on future drug design and inhibitor optimization to accelerate the discovery process of STAT3 inhibitors or degraders.
引用
收藏
页码:8884 / 8915
页数:32
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