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Regulation and function of AMPK in physiology and diseases

5′-adenosine monophosphate (AMP)-activated protein kinase (AMPK) is an evolutionarily conserved serine/threonine kinase that was originally identified as the key player in maintaining cellular energy homeostasis. Intensive research over the last decade has identified diverse molecular mechanisms and...

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Autor principal: Jeon, Sang-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973318/
https://www.ncbi.nlm.nih.gov/pubmed/27416781
http://dx.doi.org/10.1038/emm.2016.81
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author Jeon, Sang-Min
author_facet Jeon, Sang-Min
author_sort Jeon, Sang-Min
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description 5′-adenosine monophosphate (AMP)-activated protein kinase (AMPK) is an evolutionarily conserved serine/threonine kinase that was originally identified as the key player in maintaining cellular energy homeostasis. Intensive research over the last decade has identified diverse molecular mechanisms and physiological conditions that regulate the AMPK activity. AMPK regulates diverse metabolic and physiological processes and is dysregulated in major chronic diseases, such as obesity, inflammation, diabetes and cancer. On the basis of its critical roles in physiology and pathology, AMPK is emerging as one of the most promising targets for both the prevention and treatment of these diseases. In this review, we discuss the current understanding of the molecular and physiological regulation of AMPK and its metabolic and physiological functions. In addition, we discuss the mechanisms underlying the versatile roles of AMPK in diabetes and cancer.
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spelling pubmed-49733182016-08-10 Regulation and function of AMPK in physiology and diseases Jeon, Sang-Min Exp Mol Med Review 5′-adenosine monophosphate (AMP)-activated protein kinase (AMPK) is an evolutionarily conserved serine/threonine kinase that was originally identified as the key player in maintaining cellular energy homeostasis. Intensive research over the last decade has identified diverse molecular mechanisms and physiological conditions that regulate the AMPK activity. AMPK regulates diverse metabolic and physiological processes and is dysregulated in major chronic diseases, such as obesity, inflammation, diabetes and cancer. On the basis of its critical roles in physiology and pathology, AMPK is emerging as one of the most promising targets for both the prevention and treatment of these diseases. In this review, we discuss the current understanding of the molecular and physiological regulation of AMPK and its metabolic and physiological functions. In addition, we discuss the mechanisms underlying the versatile roles of AMPK in diabetes and cancer. Nature Publishing Group 2016-07 2016-07-15 /pmc/articles/PMC4973318/ /pubmed/27416781 http://dx.doi.org/10.1038/emm.2016.81 Text en Copyright © 2016 KSBMB. http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Review
Jeon, Sang-Min
Regulation and function of AMPK in physiology and diseases
title Regulation and function of AMPK in physiology and diseases
title_full Regulation and function of AMPK in physiology and diseases
title_fullStr Regulation and function of AMPK in physiology and diseases
title_full_unstemmed Regulation and function of AMPK in physiology and diseases
title_short Regulation and function of AMPK in physiology and diseases
title_sort regulation and function of ampk in physiology and diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973318/
https://www.ncbi.nlm.nih.gov/pubmed/27416781
http://dx.doi.org/10.1038/emm.2016.81
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