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Role of ADGRG1/GPR56 in Tumor Progression
Cellular communication plays a critical role in diverse aspects of tumorigenesis including tumor cell growth/death, adhesion/detachment, migration/invasion, angiogenesis, and metastasis. G protein-coupled receptors (GPCRs) which constitute the largest group of cell surface receptors are known to pla...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8699533/ https://www.ncbi.nlm.nih.gov/pubmed/34943858 http://dx.doi.org/10.3390/cells10123352 |
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author | Ng, Kwai-Fong Chen, Tse-Ching Stacey, Martin Lin, Hsi-Hsien |
author_facet | Ng, Kwai-Fong Chen, Tse-Ching Stacey, Martin Lin, Hsi-Hsien |
author_sort | Ng, Kwai-Fong |
collection | PubMed |
description | Cellular communication plays a critical role in diverse aspects of tumorigenesis including tumor cell growth/death, adhesion/detachment, migration/invasion, angiogenesis, and metastasis. G protein-coupled receptors (GPCRs) which constitute the largest group of cell surface receptors are known to play fundamental roles in all these processes. When considering the importance of GPCRs in tumorigenesis, the adhesion GPCRs (aGPCRs) are unique due to their hybrid structural organization of a long extracellular cell-adhesive domain and a seven-transmembrane signaling domain. Indeed, aGPCRs have been increasingly shown to be associated with tumor development by participating in tumor cell interaction and signaling. ADGRG1/GPR56, a representative tumor-associated aGPCR, is recognized as a potential biomarker/prognostic factor of specific cancer types with both tumor-suppressive and tumor-promoting functions. We summarize herein the latest findings of the role of ADGRG1/GPR56 in tumor progression. |
format | Online Article Text |
id | pubmed-8699533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86995332021-12-24 Role of ADGRG1/GPR56 in Tumor Progression Ng, Kwai-Fong Chen, Tse-Ching Stacey, Martin Lin, Hsi-Hsien Cells Review Cellular communication plays a critical role in diverse aspects of tumorigenesis including tumor cell growth/death, adhesion/detachment, migration/invasion, angiogenesis, and metastasis. G protein-coupled receptors (GPCRs) which constitute the largest group of cell surface receptors are known to play fundamental roles in all these processes. When considering the importance of GPCRs in tumorigenesis, the adhesion GPCRs (aGPCRs) are unique due to their hybrid structural organization of a long extracellular cell-adhesive domain and a seven-transmembrane signaling domain. Indeed, aGPCRs have been increasingly shown to be associated with tumor development by participating in tumor cell interaction and signaling. ADGRG1/GPR56, a representative tumor-associated aGPCR, is recognized as a potential biomarker/prognostic factor of specific cancer types with both tumor-suppressive and tumor-promoting functions. We summarize herein the latest findings of the role of ADGRG1/GPR56 in tumor progression. MDPI 2021-11-29 /pmc/articles/PMC8699533/ /pubmed/34943858 http://dx.doi.org/10.3390/cells10123352 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Ng, Kwai-Fong Chen, Tse-Ching Stacey, Martin Lin, Hsi-Hsien Role of ADGRG1/GPR56 in Tumor Progression |
title | Role of ADGRG1/GPR56 in Tumor Progression |
title_full | Role of ADGRG1/GPR56 in Tumor Progression |
title_fullStr | Role of ADGRG1/GPR56 in Tumor Progression |
title_full_unstemmed | Role of ADGRG1/GPR56 in Tumor Progression |
title_short | Role of ADGRG1/GPR56 in Tumor Progression |
title_sort | role of adgrg1/gpr56 in tumor progression |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8699533/ https://www.ncbi.nlm.nih.gov/pubmed/34943858 http://dx.doi.org/10.3390/cells10123352 |
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