Literature DB >> 24292842

Arrestins as regulatory hubs in cancer signalling pathways.

Hervé Enslen1, Evelyne Lima-Fernandes, Mark G H Scott.   

Abstract

Non-visual arrestins were initially appreciated for the roles they play in the negative regulation of G protein-coupled receptors through the processes of desensitisation and endocytosis. The arrestins are also now known as protein scaffolding platforms that act downstream of multiple types of receptors, ensuring relevant transmission of information for an appropriate cellular response. They function as regulatory hubs in several important signalling pathways that are often dysregulated in human cancers. Interestingly, several recent studies have documented changes in expression and localisation of arrestins that occur during cancer progression and that correlate with clinical outcome. Here, we discuss these advances and how changes in expression/localisation may affect functional outputs of arrestins in cancer biology.

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 24292842     DOI: 10.1007/978-3-642-41199-1_21

Source DB:  PubMed          Journal:  Handb Exp Pharmacol        ISSN: 0171-2004


  4 in total

1.  The RanBP2/RanGAP1-SUMO complex gates β-arrestin2 nuclear entry to regulate the Mdm2-p53 signaling axis.

Authors:  Elodie Blondel-Tepaz; Marie Leverve; Badr Sokrat; Justine S Paradis; Milena Kosic; Kusumika Saha; Cédric Auffray; Evelyne Lima-Fernandes; Alessia Zamborlini; Anne Poupon; Louis Gaboury; Jane Findlay; George S Baillie; Hervé Enslen; Michel Bouvier; Stéphane Angers; Stefano Marullo; Mark G H Scott
Journal:  Oncogene       Date:  2021-03-01       Impact factor: 9.867

2.  PTEN controls glandular morphogenesis through a juxtamembrane β-Arrestin1/ARHGAP21 scaffolding complex.

Authors:  Arman Javadi; Ravi K Deevi; Emma Evergren; Elodie Blondel-Tepaz; George S Baillie; Mark Gh Scott; Frederick C Campbell
Journal:  Elife       Date:  2017-07-27       Impact factor: 8.140

Review 3.  The role and mechanism of β‑arrestins in cancer invasion and metastasis (Review).

Authors:  Qing Song; Qing Ji; Qi Li
Journal:  Int J Mol Med       Date:  2017-11-27       Impact factor: 4.101

4.  β-arrestin1-medieated inhibition of FOXO3a contributes to prostate cancer cell growth in vitro and in vivo.

Authors:  Zhenzhen Kong; Tuo Deng; Mengping Zhang; Zhijian Zhao; Yang Liu; Lianmin Luo; Chao Cai; Wenqi Wu; Xiaolu Duan
Journal:  Cancer Sci       Date:  2018-05-26       Impact factor: 6.716

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.