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Protease-Activated Receptors and other G-Protein-Coupled Receptors: the Melanoma Connection

The vast array of G-protein-coupled receptors (GPCRs) play crucial roles in both physiological and pathological processes, including vision, coagulation, inflammation, autophagy, and cell proliferation. GPCRs also affect processes that augment cell proliferation and metastases in many cancers includ...

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Detalles Bibliográficos
Autores principales: Rosero, Rebecca A., Villares, Gabriel J., Bar-Eli, Menashe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4908108/
https://www.ncbi.nlm.nih.gov/pubmed/27379162
http://dx.doi.org/10.3389/fgene.2016.00112
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author Rosero, Rebecca A.
Villares, Gabriel J.
Bar-Eli, Menashe
author_facet Rosero, Rebecca A.
Villares, Gabriel J.
Bar-Eli, Menashe
author_sort Rosero, Rebecca A.
collection PubMed
description The vast array of G-protein-coupled receptors (GPCRs) play crucial roles in both physiological and pathological processes, including vision, coagulation, inflammation, autophagy, and cell proliferation. GPCRs also affect processes that augment cell proliferation and metastases in many cancers including melanoma. Melanoma is the deadliest form of skin cancer, yet limited therapeutic modalities are available to patients with metastatic melanoma. Studies have found that both chemokine receptors and protease-activated receptors, both of which are GPCRs, are central to the metastatic melanoma phenotype and may serve as potential targets in novel therapies against melanoma and other cancers.
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spelling pubmed-49081082016-07-04 Protease-Activated Receptors and other G-Protein-Coupled Receptors: the Melanoma Connection Rosero, Rebecca A. Villares, Gabriel J. Bar-Eli, Menashe Front Genet Genetics The vast array of G-protein-coupled receptors (GPCRs) play crucial roles in both physiological and pathological processes, including vision, coagulation, inflammation, autophagy, and cell proliferation. GPCRs also affect processes that augment cell proliferation and metastases in many cancers including melanoma. Melanoma is the deadliest form of skin cancer, yet limited therapeutic modalities are available to patients with metastatic melanoma. Studies have found that both chemokine receptors and protease-activated receptors, both of which are GPCRs, are central to the metastatic melanoma phenotype and may serve as potential targets in novel therapies against melanoma and other cancers. Frontiers Media S.A. 2016-06-15 /pmc/articles/PMC4908108/ /pubmed/27379162 http://dx.doi.org/10.3389/fgene.2016.00112 Text en Copyright © 2016 Rosero, Villares and Bar-Eli. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Rosero, Rebecca A.
Villares, Gabriel J.
Bar-Eli, Menashe
Protease-Activated Receptors and other G-Protein-Coupled Receptors: the Melanoma Connection
title Protease-Activated Receptors and other G-Protein-Coupled Receptors: the Melanoma Connection
title_full Protease-Activated Receptors and other G-Protein-Coupled Receptors: the Melanoma Connection
title_fullStr Protease-Activated Receptors and other G-Protein-Coupled Receptors: the Melanoma Connection
title_full_unstemmed Protease-Activated Receptors and other G-Protein-Coupled Receptors: the Melanoma Connection
title_short Protease-Activated Receptors and other G-Protein-Coupled Receptors: the Melanoma Connection
title_sort protease-activated receptors and other g-protein-coupled receptors: the melanoma connection
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4908108/
https://www.ncbi.nlm.nih.gov/pubmed/27379162
http://dx.doi.org/10.3389/fgene.2016.00112
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