Literature DB >> 32089163

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

Arun K Shukla1, Hemlata Dwivedi-Agnihotri2.   

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.
© 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Allosteric modulators; Biased agonism; Breast cancer; Cellular signaling; Endocytosis; GPCRs; Protein-protein interaction; β-Arrestins

Mesh:

Substances:

Year:  2020        PMID: 32089163      PMCID: PMC7115872          DOI: 10.1016/bs.acr.2020.01.001

Source DB:  PubMed          Journal:  Adv Cancer Res        ISSN: 0065-230X            Impact factor:   6.242


  88 in total

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Journal:  Mol Pharmacol       Date:  2017-02-28       Impact factor: 4.436

2.  β-arrestin 2 is associated with multidrug resistance in breast cancer cells through regulating MDR1 gene expression.

Authors:  Xuanxuan Jing; Hui Zhang; Jing Hu; Peng Su; Wei Zhang; Ming Jia; Hongxia Cheng; Weiwei Li; Gengyin Zhou
Journal:  Int J Clin Exp Pathol       Date:  2015-02-01

3.  Trafficking and function of GPCRs in the endosomal compartment.

Authors:  Davide Calebiro; Amod Godbole; Sandra Lyga; Martin J Lohse
Journal:  Methods Mol Biol       Date:  2015

4.  Angiotensin II activates CaV 1.2 Ca2+ channels through β-arrestin2 and casein kinase 2 in mouse immature cardiomyocytes.

Authors:  Toshihide Kashihara; Tsutomu Nakada; Katsuhiko Kojima; Toshikazu Takeshita; Mitsuhiko Yamada
Journal:  J Physiol       Date:  2017-04-20       Impact factor: 5.182

5.  Beta-arrestin/Ral signaling regulates lysophosphatidic acid-mediated migration and invasion of human breast tumor cells.

Authors:  Timothy T Li; Mistre Alemayehu; Adel I Aziziyeh; Cynthia Pape; Macarena Pampillo; Lynne-Marie Postovit; Gordon B Mills; Andy V Babwah; Moshmi Bhattacharya
Journal:  Mol Cancer Res       Date:  2009-07       Impact factor: 5.852

6.  Distinct phosphorylation sites on the β(2)-adrenergic receptor establish a barcode that encodes differential functions of β-arrestin.

Authors:  Kelly N Nobles; Kunhong Xiao; Seungkirl Ahn; Arun K Shukla; Christopher M Lam; Sudarshan Rajagopal; Ryan T Strachan; Teng-Yi Huang; Erin A Bressler; Makoto R Hara; Sudha K Shenoy; Steven P Gygi; Robert J Lefkowitz
Journal:  Sci Signal       Date:  2011-08-09       Impact factor: 8.192

7.  Arrestin Domain Containing 3 Reverses Epithelial to Mesenchymal Transition and Chemo-Resistance of TNBC Cells by Up-Regulating Expression of miR-200b.

Authors:  Young Hwa Soung; Heesung Chung; Cecilia Yan; Jingfang Ju; Jun Chung
Journal:  Cells       Date:  2019-07-10       Impact factor: 6.600

Review 8.  Below the Surface: IGF-1R Therapeutic Targeting and Its Endocytic Journey.

Authors:  Caitrin Crudden; Dawei Song; Sonia Cismas; Eric Trocmé; Sylvya Pasca; George A Calin; Ada Girnita; Leonard Girnita
Journal:  Cells       Date:  2019-10-09       Impact factor: 6.600

9.  Molecular mechanism of modulating arrestin conformation by GPCR phosphorylation.

Authors:  Andrija Sente; Raphael Peer; Ashish Srivastava; Mithu Baidya; Arthur M Lesk; Santhanam Balaji; Arun K Shukla; M Madan Babu; Tilman Flock
Journal:  Nat Struct Mol Biol       Date:  2018-06-05       Impact factor: 15.369

10.  A synthetic intrabody-based selective and generic inhibitor of GPCR endocytosis.

Authors:  Eshan Ghosh; Ashish Srivastava; Mithu Baidya; Punita Kumari; Hemlata Dwivedi; Kumari Nidhi; Ravi Ranjan; Shalini Dogra; Akiko Koide; Prem N Yadav; Sachdev S Sidhu; Shohei Koide; Arun K Shukla
Journal:  Nat Nanotechnol       Date:  2017-10-02       Impact factor: 39.213

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  3 in total

Review 1.  The Role of β-Arrestins in Regulating Stem Cell Phenotypes in Normal and Tumorigenic Cells.

Authors:  Georgios Kallifatidis; Kenza Mamouni; Bal L Lokeshwar
Journal:  Int J Mol Sci       Date:  2020-12-07       Impact factor: 5.923

Review 2.  Endomembrane-Based Signaling by GPCRs and G-Proteins.

Authors:  Federica Liccardo; Alberto Luini; Rosaria Di Martino
Journal:  Cells       Date:  2022-02-03       Impact factor: 6.600

3.  Exploring GPCR-arrestin interfaces with genetically encoded crosslinkers.

Authors:  Thore Böttke; Stefan Ernicke; Robert Serfling; Christian Ihling; Edyta Burda; Vsevolod V Gurevich; Andrea Sinz; Irene Coin
Journal:  EMBO Rep       Date:  2020-09-14       Impact factor: 8.807

  3 in total

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