The structure and regulation of the E3 ubiquitin ligase HUWE1 and its biological functions in cancer

被引:0
|
作者
Xiaofeng Gong
Danyu Du
Yanran Deng
Yuqi Zhou
Li Sun
Shengtao Yuan
机构
[1] China Pharmaceutical University,Jiangsu Key Laboratory of Drug Screening
[2] China Pharmaceutical University,Jiangsu Center for Pharmacodynamics Research and Evaluation
来源
Investigational New Drugs | 2020年 / 38卷
关键词
Ubiquitination; HUWE1; Cancer therapeutics; Drug discovery;
D O I
暂无
中图分类号
学科分类号
摘要
E3 ligases are a class of critical enzymes that can catalyse the transfer of ubiquitin (Ub) from an E2 enzyme to the substrate and are essential to cellular processes. The E3 ligase HUWE1 (also known as ARF-BP1, HECTH9, HSPC272, Ib772, LASU1, MULE, URE-B1, UREB1, and HECT, UBA and WWE domain-containing E3 ubiquitin protein ligase 1) is encoded by the huwe1 gene. HUWE1 is a key regulator of the DNA damage response, transcription, autophagy, apoptosis and metabolism in a variety of cancers. Due to its pivotal role in conferring substrate specificity, HUWE1 has attracted enormous attention as a promising anticancer drug target. In this review, we indicate the specific molecular structure of HUWE1 and its role in various cellular signalling pathways and highlight new insights into HUWE1 in cancer. Finally, we discuss outstanding questions regarding HUWE1 in oncology and highlight its limitations in drug development and clinical guidance to better define the role of HUWE1 in multiple cancers.
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页码:515 / 524
页数:9
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