Structure and function of β-arrestins, their emerging role in breast cancer, and potential opportunities for therapeutic manipulation

被引:10
|
作者
Shukla, Arun K. [1 ]
Dwivedi-Agnihotri, Hemlata [1 ]
机构
[1] Indian Inst Technol, Dept Biol Sci & Bioengn, Kanpur, Uttar Pradesh, India
来源
GPCR SIGNALING IN CANCER | 2020年 / 145卷
基金
英国惠康基金;
关键词
INTERNATIONAL UNION; CHEMOKINE RECEPTORS; CLATHRIN ADAPTER; CELL; PROGRESSION; BETA-ARRESTIN-1; NOMENCLATURE; TRAFFICKING; PROTEINS; INVASION;
D O I
10.1016/bs.acr.2020.01.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
beta-Arrestins (beta arrs) are multifunctional intracellular proteins with an ability to directly interact with a large number of cellular partners including the G protein-coupled receptors (GPCRs). beta arrs contribute to multiple aspects of GPCR signaling, trafficking and downregulation. Considering the central involvement of GPCR signaling in the onset and progression of diverse types of cancers, beta arrs have also emerged as key players in the context of investigating cancer phenotypes, and as potential therapeutic targets. In this chapter, we first provide a brief account of structure and function of beta arrs and then highlight recent discoveries unfolding novel functional attributes of beta arrs in breast cancer. We also underscore the recent paradigms of modulating beta arr functions in cellular context and potential therapeutic opportunities going forward.
引用
收藏
页码:139 / 156
页数:18
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