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A complex structure of arrestin-2 bound to a G protein-coupled receptor.一种与G蛋白偶联受体结合的视紫红质抑制蛋白-2的复杂结构。
Cell Res. 2019 Dec;29(12):971-983. doi: 10.1038/s41422-019-0256-2. Epub 2019 Nov 27.
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Advances in the discovery of microRNA-based anticancer therapeutics: latest tools and developments.基于 microRNA 的抗癌治疗药物的发现进展:最新工具和进展。
Expert Opin Drug Discov. 2020 Jan;15(1):63-83. doi: 10.1080/17460441.2020.1690449. Epub 2019 Nov 19.
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Below the Surface: IGF-1R Therapeutic Targeting and Its Endocytic Journey.深入剖析:IGF-1R 治疗靶点及其内吞途径。
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Conformational Sensors and Domain Swapping Reveal Structural and Functional Differences between β-Arrestin Isoforms.构象传感器和结构域交换揭示β-arrestin 异构体的结构和功能差异。
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Targeting Endothelin-1 Receptor/β-Arrestin-1 Axis in Ovarian Cancer: From Basic Research to a Therapeutic Approach.靶向卵巢癌中的内皮素-1受体/β-抑制蛋白-1轴:从基础研究到治疗方法
Front Endocrinol (Lausanne). 2019 Sep 4;10:609. doi: 10.3389/fendo.2019.00609. eCollection 2019.
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Arrestin-3 interaction with maternal embryonic leucine-zipper kinase.抑制素结合蛋白与母源性胚胎亮氨酸拉链激酶相互作用
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miR-374a-5p promotes tumor progression by targeting ARRB1 in triple negative breast cancer.miR-374a-5p 通过靶向三阴性乳腺癌中的 ARRB1 促进肿瘤进展。
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GPCR Signaling Regulation: The Role of GRKs and Arrestins.G蛋白偶联受体信号转导调控:G蛋白偶联受体激酶和抑制蛋白的作用
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β-arrestins 的结构与功能、它们在乳腺癌中的新作用,以及治疗干预的潜在机会。

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

机构信息

Department of Biological Sciences and Bioengineering, Indian Institute of Technology, Kanpur, India.

Department of Biological Sciences and Bioengineering, Indian Institute of Technology, Kanpur, India.

出版信息

Adv Cancer Res. 2020;145:139-156. doi: 10.1016/bs.acr.2020.01.001. Epub 2020 Feb 5.

DOI:10.1016/bs.acr.2020.01.001
PMID:32089163
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7115872/
Abstract

β-Arrestins (βarrs) are multifunctional intracellular proteins with an ability to directly interact with a large number of cellular partners including the G protein-coupled receptors (GPCRs). βarrs 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, βarrs 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 βarrs and then highlight recent discoveries unfolding novel functional attributes of βarrs in breast cancer. We also underscore the recent paradigms of modulating βarr functions in cellular context and potential therapeutic opportunities going forward.

摘要

β-arrestins(βarrs)是具有多功能的细胞内蛋白,能够直接与包括 G 蛋白偶联受体(GPCRs)在内的大量细胞伴侣相互作用。βarrs 有助于 GPCR 信号转导、运输和下调的多个方面。考虑到 GPCR 信号转导在多种类型癌症的发生和进展中的核心作用,βarrs 也已成为研究癌症表型的关键因素,并成为潜在的治疗靶点。在本章中,我们首先简要介绍 βarrs 的结构和功能,然后重点介绍βarrs 在乳腺癌中发挥新功能的最新发现。我们还强调了在细胞环境中调节βarr 功能的最新范例以及未来的潜在治疗机会。