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Focusing on Adenosine Receptors as a Potential Targeted Therapy in Human Diseases

Adenosine is involved in a range of physiological and pathological effects through membrane-bound receptors linked to G proteins. There are four subtypes of adenosine receptors, described as A(1)AR, A(2A)AR, A(2B)AR, and A(3)AR, which are the center of cAMP signal pathway-based drug development. Sev...

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Autores principales: Effendi, Wiwin Is, Nagano, Tatsuya, Kobayashi, Kazuyuki, Nishimura, Yoshihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140859/
https://www.ncbi.nlm.nih.gov/pubmed/32213945
http://dx.doi.org/10.3390/cells9030785
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author Effendi, Wiwin Is
Nagano, Tatsuya
Kobayashi, Kazuyuki
Nishimura, Yoshihiro
author_facet Effendi, Wiwin Is
Nagano, Tatsuya
Kobayashi, Kazuyuki
Nishimura, Yoshihiro
author_sort Effendi, Wiwin Is
collection PubMed
description Adenosine is involved in a range of physiological and pathological effects through membrane-bound receptors linked to G proteins. There are four subtypes of adenosine receptors, described as A(1)AR, A(2A)AR, A(2B)AR, and A(3)AR, which are the center of cAMP signal pathway-based drug development. Several types of agonists, partial agonists or antagonists, and allosteric substances have been synthesized from these receptors as new therapeutic drug candidates. Research efforts surrounding A(1)AR and A(2A)AR are perhaps the most enticing because of their concentration and affinity; however, as a consequence of distressing conditions, both A(2B)AR and A(3)AR levels might accumulate. This review focuses on the biological features of each adenosine receptor as the basis of ligand production and describes clinical studies of adenosine receptor-associated pharmaceuticals in human diseases.
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spelling pubmed-71408592020-04-10 Focusing on Adenosine Receptors as a Potential Targeted Therapy in Human Diseases Effendi, Wiwin Is Nagano, Tatsuya Kobayashi, Kazuyuki Nishimura, Yoshihiro Cells Review Adenosine is involved in a range of physiological and pathological effects through membrane-bound receptors linked to G proteins. There are four subtypes of adenosine receptors, described as A(1)AR, A(2A)AR, A(2B)AR, and A(3)AR, which are the center of cAMP signal pathway-based drug development. Several types of agonists, partial agonists or antagonists, and allosteric substances have been synthesized from these receptors as new therapeutic drug candidates. Research efforts surrounding A(1)AR and A(2A)AR are perhaps the most enticing because of their concentration and affinity; however, as a consequence of distressing conditions, both A(2B)AR and A(3)AR levels might accumulate. This review focuses on the biological features of each adenosine receptor as the basis of ligand production and describes clinical studies of adenosine receptor-associated pharmaceuticals in human diseases. MDPI 2020-03-24 /pmc/articles/PMC7140859/ /pubmed/32213945 http://dx.doi.org/10.3390/cells9030785 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Effendi, Wiwin Is
Nagano, Tatsuya
Kobayashi, Kazuyuki
Nishimura, Yoshihiro
Focusing on Adenosine Receptors as a Potential Targeted Therapy in Human Diseases
title Focusing on Adenosine Receptors as a Potential Targeted Therapy in Human Diseases
title_full Focusing on Adenosine Receptors as a Potential Targeted Therapy in Human Diseases
title_fullStr Focusing on Adenosine Receptors as a Potential Targeted Therapy in Human Diseases
title_full_unstemmed Focusing on Adenosine Receptors as a Potential Targeted Therapy in Human Diseases
title_short Focusing on Adenosine Receptors as a Potential Targeted Therapy in Human Diseases
title_sort focusing on adenosine receptors as a potential targeted therapy in human diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140859/
https://www.ncbi.nlm.nih.gov/pubmed/32213945
http://dx.doi.org/10.3390/cells9030785
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