Literature DB >> 27818281

GPR56/ADGRG1 Activation Promotes Melanoma Cell Migration via NTF Dissociation and CTF-Mediated Gα12/13/RhoA Signaling.

Nien-Yi Chiang1, Yen-Ming Peng2, Horng-Heng Juang3, Tse-Ching Chen4, Hsiao-Lin Pan2, Gin-Wen Chang1, Hsi-Hsien Lin5.   

Abstract

GPR56/ADGRG1 is a versatile adhesion G protein-coupled receptor with diverse biological functions. GPR56 expression is variably detected in human melanoma cell lines and correlates inversely with the metastatic potential of melanoma lesions. GPR56 associates with the tetraspanins CD9 and CD81 on the melanoma cell surface. GPR56 activation by immobilized CG4 monoclonal antibody facilitates N-terminal fragment dissociation in a CD9/CD81-dependent manner specifically inducing IL-6 production, which promotes cell migration and invasion. Interestingly, expression of GPR56-C-terminal fragment alone recapitulates the antibody-induced receptor function, implicating a major role for the C-terminal fragment in GPR56 activation and signaling. Analysis of site-directed mutant receptors attests the importance of the conserved N-terminal residues of the C-terminal fragment for its self-activation. Finally, we show that the GPR56-induced signaling in melanoma cells is mediated by the Gα12/13/RhoA pathway. In summary, the expression and activation of GPR56 may modulate melanoma progression in part by inducing IL-6 production after N-terminal fragment dissociation and C-terminal fragment self-activation.
Copyright © 2016 The Authors. Published by Elsevier Inc. All rights reserved.

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Year:  2016        PMID: 27818281     DOI: 10.1016/j.jid.2016.10.031

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  19 in total

1.  Disease-associated extracellular loop mutations in the adhesion G protein-coupled receptor G1 (ADGRG1; GPR56) differentially regulate downstream signaling.

Authors:  Ayush Kishore; Randy A Hall
Journal:  J Biol Chem       Date:  2017-04-19       Impact factor: 5.157

2.  Stachel-independent modulation of GPR56/ADGRG1 signaling by synthetic ligands directed to its extracellular region.

Authors:  Gabriel S Salzman; Shu Zhang; Ankit Gupta; Akiko Koide; Shohei Koide; Demet Araç
Journal:  Proc Natl Acad Sci U S A       Date:  2017-09-05       Impact factor: 11.205

Review 3.  The Emerging Role of Adhesion GPCRs in Cancer.

Authors:  Abanoub A Gad; Nariman Balenga
Journal:  ACS Pharmacol Transl Sci       Date:  2020-01-13

Review 4.  Adhesion GPCRs as a paradigm for understanding polycystin-1 G protein regulation.

Authors:  Robin L Maser; James P Calvet
Journal:  Cell Signal       Date:  2020-04-16       Impact factor: 4.315

5.  Regulation of pulmonary surfactant by the adhesion GPCR GPR116/ADGRF5 requires a tethered agonist-mediated activation mechanism.

Authors:  James P Bridges; Caterina Safina; Bernard Pirard; Kari Brown; Alyssa Filuta; Ravichandran Panchanathan; Rochdi Bouhelal; Nicole Reymann; Sejal Patel; Klaus Seuwen; William E Miller; Marie-Gabrielle Ludwig
Journal:  Elife       Date:  2022-09-08       Impact factor: 8.713

6.  The Novel Immune Checkpoint GPR56 Is Expressed on Tumor-Infiltrating Lymphocytes and Selectively Upregulated upon TCR Signaling.

Authors:  Vrouyr Bilemjian; Martijn R Vlaming; Jimena Álvarez Freile; Gerwin Huls; Marco De Bruyn; Edwin Bremer
Journal:  Cancers (Basel)       Date:  2022-06-28       Impact factor: 6.575

Review 7.  Adhesion G protein-coupled receptors: structure, signaling, physiology, and pathophysiology.

Authors:  Trisha Lala; Randy A Hall
Journal:  Physiol Rev       Date:  2022-04-25       Impact factor: 46.500

8.  Cancer Cell Mechanics: Adhesion G Protein-coupled Receptors in Action?

Authors:  Nicole Scholz
Journal:  Front Oncol       Date:  2018-03-13       Impact factor: 6.244

9.  Activation of Adhesion GPCR EMR2/ADGRE2 Induces Macrophage Differentiation and Inflammatory Responses via16/Akt/MAPK/NF-κB Signaling Pathways.

Authors:  Kuan-Yu I; Yi-Shu Huang; Ching-Hsun Hu; Wen-Yi Tseng; Chia-Hsin Cheng; Martin Stacey; Siamon Gordon; Gin-Wen Chang; Hsi-Hsien Lin
Journal:  Front Immunol       Date:  2017-04-03       Impact factor: 7.561

10.  The Adhesion G-Protein-Coupled Receptor, GPR56/ADGRG1, Inhibits Cell-Extracellular Matrix Signaling to Prevent Metastatic Melanoma Growth.

Authors:  Michelle W Millar; Nancy Corson; Lei Xu
Journal:  Front Oncol       Date:  2018-02-01       Impact factor: 6.244

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