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GPR35 as a Novel Therapeutic Target

G protein-coupled receptors (GPCRs) remain the best studied class of cell surface receptors and the most tractable family of proteins for novel small molecule drug discovery. Despite this, a considerable number of GPCRs remain poorly characterized and in a significant number of cases, endogenous lig...

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Autores principales: MacKenzie, A. E., Lappin, J. E., Taylor, D. L., Nicklin, S. A., Milligan, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3356001/
https://www.ncbi.nlm.nih.gov/pubmed/22654822
http://dx.doi.org/10.3389/fendo.2011.00068
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author MacKenzie, A. E.
Lappin, J. E.
Taylor, D. L.
Nicklin, S. A.
Milligan, G.
author_facet MacKenzie, A. E.
Lappin, J. E.
Taylor, D. L.
Nicklin, S. A.
Milligan, G.
author_sort MacKenzie, A. E.
collection PubMed
description G protein-coupled receptors (GPCRs) remain the best studied class of cell surface receptors and the most tractable family of proteins for novel small molecule drug discovery. Despite this, a considerable number of GPCRs remain poorly characterized and in a significant number of cases, endogenous ligand(s) that activate them remain undefined or are of questionable physiological relevance. GPR35 was initially discovered over a decade ago but has remained an “orphan” receptor. Recent publications have highlighted novel ligands, both endogenously produced and synthetic, which demonstrate significant potency at this receptor. Furthermore, evidence is accumulating which highlights potential roles for GPR35 in disease and therefore, efforts to characterize GPR35 more fully and develop it as a novel therapeutic target in conditions that range from diabetes and hypertension to asthma are increasing. Recently identified ligands have shown marked species selective properties, indicating major challenges for future drug development. As we begin to understand these issues, the continuing efforts to identify novel agonist and antagonist ligands for GPR35 will help to decipher its true physiological relevance; translating multiple assay systems in vitro, to animal disease systems in vivo and finally to man.
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spelling pubmed-33560012012-05-31 GPR35 as a Novel Therapeutic Target MacKenzie, A. E. Lappin, J. E. Taylor, D. L. Nicklin, S. A. Milligan, G. Front Endocrinol (Lausanne) Endocrinology G protein-coupled receptors (GPCRs) remain the best studied class of cell surface receptors and the most tractable family of proteins for novel small molecule drug discovery. Despite this, a considerable number of GPCRs remain poorly characterized and in a significant number of cases, endogenous ligand(s) that activate them remain undefined or are of questionable physiological relevance. GPR35 was initially discovered over a decade ago but has remained an “orphan” receptor. Recent publications have highlighted novel ligands, both endogenously produced and synthetic, which demonstrate significant potency at this receptor. Furthermore, evidence is accumulating which highlights potential roles for GPR35 in disease and therefore, efforts to characterize GPR35 more fully and develop it as a novel therapeutic target in conditions that range from diabetes and hypertension to asthma are increasing. Recently identified ligands have shown marked species selective properties, indicating major challenges for future drug development. As we begin to understand these issues, the continuing efforts to identify novel agonist and antagonist ligands for GPR35 will help to decipher its true physiological relevance; translating multiple assay systems in vitro, to animal disease systems in vivo and finally to man. Frontiers Research Foundation 2011-11-09 /pmc/articles/PMC3356001/ /pubmed/22654822 http://dx.doi.org/10.3389/fendo.2011.00068 Text en Copyright © 2011 MacKenzie, Lappin, Taylor, Nicklin and Milligan. http://www.frontiersin.org/licenseagreement This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.
spellingShingle Endocrinology
MacKenzie, A. E.
Lappin, J. E.
Taylor, D. L.
Nicklin, S. A.
Milligan, G.
GPR35 as a Novel Therapeutic Target
title GPR35 as a Novel Therapeutic Target
title_full GPR35 as a Novel Therapeutic Target
title_fullStr GPR35 as a Novel Therapeutic Target
title_full_unstemmed GPR35 as a Novel Therapeutic Target
title_short GPR35 as a Novel Therapeutic Target
title_sort gpr35 as a novel therapeutic target
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3356001/
https://www.ncbi.nlm.nih.gov/pubmed/22654822
http://dx.doi.org/10.3389/fendo.2011.00068
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