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AMP-activated protein kinase: a target for drugs both ancient and modern
The AMP-activated protein kinase (AMPK) is a sensor of cellular energy status. It is activated, by a mechanism requiring the tumor suppressor LKB1, by metabolic stresses that increase cellular ADP:ATP and/or AMP:ATP ratios. Once activated, it switches on catabolic pathways that generate ATP, while s...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722193/ https://www.ncbi.nlm.nih.gov/pubmed/23102217 http://dx.doi.org/10.1016/j.chembiol.2012.08.019 |
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author | Hardie, D. Grahame Ross, Fiona A. Hawley, Simon A. |
author_facet | Hardie, D. Grahame Ross, Fiona A. Hawley, Simon A. |
author_sort | Hardie, D. Grahame |
collection | PubMed |
description | The AMP-activated protein kinase (AMPK) is a sensor of cellular energy status. It is activated, by a mechanism requiring the tumor suppressor LKB1, by metabolic stresses that increase cellular ADP:ATP and/or AMP:ATP ratios. Once activated, it switches on catabolic pathways that generate ATP, while switching off biosynthetic pathways and cell cycle progress. These effects suggest that AMPK activators might be useful for treatment and/or prevention of type 2 diabetes and cancer. Indeed, AMPK is activated by the drugs metformin and salicylate, the latter being the major breakdown product of aspirin. Metformin is widely used to treat diabetes, while there is epidemiological evidence that both metformin and aspirin provide protection against cancer. We review the mechanisms of AMPK activation by these and other drugs, and by natural products derived from traditional herbal medicines. |
format | Online Article Text |
id | pubmed-5722193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
record_format | MEDLINE/PubMed |
spelling | pubmed-57221932017-12-08 AMP-activated protein kinase: a target for drugs both ancient and modern Hardie, D. Grahame Ross, Fiona A. Hawley, Simon A. Chem Biol Article The AMP-activated protein kinase (AMPK) is a sensor of cellular energy status. It is activated, by a mechanism requiring the tumor suppressor LKB1, by metabolic stresses that increase cellular ADP:ATP and/or AMP:ATP ratios. Once activated, it switches on catabolic pathways that generate ATP, while switching off biosynthetic pathways and cell cycle progress. These effects suggest that AMPK activators might be useful for treatment and/or prevention of type 2 diabetes and cancer. Indeed, AMPK is activated by the drugs metformin and salicylate, the latter being the major breakdown product of aspirin. Metformin is widely used to treat diabetes, while there is epidemiological evidence that both metformin and aspirin provide protection against cancer. We review the mechanisms of AMPK activation by these and other drugs, and by natural products derived from traditional herbal medicines. 2012-10-26 /pmc/articles/PMC5722193/ /pubmed/23102217 http://dx.doi.org/10.1016/j.chembiol.2012.08.019 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Article Hardie, D. Grahame Ross, Fiona A. Hawley, Simon A. AMP-activated protein kinase: a target for drugs both ancient and modern |
title | AMP-activated protein kinase: a target for drugs both ancient and modern |
title_full | AMP-activated protein kinase: a target for drugs both ancient and modern |
title_fullStr | AMP-activated protein kinase: a target for drugs both ancient and modern |
title_full_unstemmed | AMP-activated protein kinase: a target for drugs both ancient and modern |
title_short | AMP-activated protein kinase: a target for drugs both ancient and modern |
title_sort | amp-activated protein kinase: a target for drugs both ancient and modern |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722193/ https://www.ncbi.nlm.nih.gov/pubmed/23102217 http://dx.doi.org/10.1016/j.chembiol.2012.08.019 |
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