Literature DB >> 33411320

The Roles of Orphan G Protein-Coupled Receptors in Autoimmune Diseases.

Mingming Zhao1, Zheyu Wang2,3, Ming Yang1, Yan Ding3,4, Ming Zhao1, Haijing Wu5, Yan Zhang6,7,8,9, Qianjin Lu10,11.   

Abstract

G protein-coupled receptors (GPCRs) constitute the largest family of plasma membrane receptors in nature and mediate the effects of a variety of extracellular signals, such as hormone, neurotransmitter, odor, and light signals. Due to their involvement in a broad range of physiological and pathological processes and their accessibility, GPCRs are widely used as pharmacological targets of treatment. Orphan G protein-coupled receptors (oGPCRs) are GPCRs for which no natural ligands have been found, and they not only play important roles in various physiological functions, such as sensory perception, reproduction, development, growth, metabolism, and responsiveness, but are also closely related to many major diseases, such as central nervous system (CNS) diseases, metabolic diseases, and cancer. Recently, many studies have reported that oGPCRs play increasingly important roles as key factors in the occurrence and progression of autoimmune diseases. Therefore, oGPCRs are likely to become potential therapeutic targets and may provide a breakthrough in the study of autoimmune diseases. In this article, we focus on reviewing the recent research progress and clinical treatment effects of oGPCRs in three common autoimmune diseases: multiple sclerosis (MS), rheumatoid arthritis (RA), and systemic lupus erythematosus (SLE), shedding light on novel strategies for treatments.

Entities:  

Keywords:  G protein-coupled receptors; Multiple sclerosis; Orphan G protein-coupled receptors; Rheumatoid arthritis; Systemic lupus erythematosus

Year:  2021        PMID: 33411320     DOI: 10.1007/s12016-020-08829-y

Source DB:  PubMed          Journal:  Clin Rev Allergy Immunol        ISSN: 1080-0549            Impact factor:   8.667


  182 in total

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Review 2.  G-protein-coupled receptors at a glance.

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Review 3.  How many drug targets are there?

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Journal:  Nat Rev Drug Discov       Date:  2006-12       Impact factor: 84.694

Review 4.  Development of autoantibodies precedes clinical manifestations of autoimmune diseases: A comprehensive review.

Authors:  Wen-Tao Ma; Christopher Chang; M Eric Gershwin; Zhe-Xiong Lian
Journal:  J Autoimmun       Date:  2017-07-21       Impact factor: 7.094

Review 5.  Structural bioinformatics analysis of variants on GPCR function.

Authors:  Syed Askar Syed Haneef; Shoba Ranganathan
Journal:  Curr Opin Struct Biol       Date:  2019-06-04       Impact factor: 6.809

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Authors:  Mengjie Lu; Beili Wu
Journal:  IUBMB Life       Date:  2016-10-20       Impact factor: 3.885

Review 7.  How Ligands Illuminate GPCR Molecular Pharmacology.

Authors:  Daniel Wacker; Raymond C Stevens; Bryan L Roth
Journal:  Cell       Date:  2017-07-27       Impact factor: 41.582

Review 8.  G Protein-Coupled Receptors as Targets for Approved Drugs: How Many Targets and How Many Drugs?

Authors:  Krishna Sriram; Paul A Insel
Journal:  Mol Pharmacol       Date:  2018-01-03       Impact factor: 4.436

Review 9.  GPCR agonists and antagonists in the clinic.

Authors:  Joel D A Tyndall; Radhika Sandilya
Journal:  Med Chem       Date:  2005-07       Impact factor: 2.745

Review 10.  Trends in GPCR drug discovery: new agents, targets and indications.

Authors:  Alexander S Hauser; Misty M Attwood; Mathias Rask-Andersen; Helgi B Schiöth; David E Gloriam
Journal:  Nat Rev Drug Discov       Date:  2017-10-27       Impact factor: 84.694

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