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Mitochondrial Sirtuin 3: New emerging biological function and therapeutic target

Sirtuin 3 (SIRT3) is one of the most prominent deacetylases that can regulate acetylation levels in mitochondria, which are essential for eukaryotic life and inextricably linked to the metabolism of multiple organs. Hitherto, SIRT3 has been substantiated to be involved in almost all aspects of mitoc...

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Autores principales: Zhang, Jin, Xiang, Honggang, Liu, Jie, Chen, Yi, He, Rong-Rong, Liu, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381741/
https://www.ncbi.nlm.nih.gov/pubmed/32724473
http://dx.doi.org/10.7150/thno.45922
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author Zhang, Jin
Xiang, Honggang
Liu, Jie
Chen, Yi
He, Rong-Rong
Liu, Bo
author_facet Zhang, Jin
Xiang, Honggang
Liu, Jie
Chen, Yi
He, Rong-Rong
Liu, Bo
author_sort Zhang, Jin
collection PubMed
description Sirtuin 3 (SIRT3) is one of the most prominent deacetylases that can regulate acetylation levels in mitochondria, which are essential for eukaryotic life and inextricably linked to the metabolism of multiple organs. Hitherto, SIRT3 has been substantiated to be involved in almost all aspects of mitochondrial metabolism and homeostasis, protecting mitochondria from a variety of damage. Accumulating evidence has recently documented that SIRT3 is associated with many types of human diseases, including age-related diseases, cancer, heart disease and metabolic diseases, indicating that SIRT3 can be a potential therapeutic target. Here we focus on summarizing the intricate mechanisms of SIRT3 in human diseases, and recent notable advances in the field of small-molecule activators or inhibitors targeting SIRT3 as well as their potential therapeutic applications for future drug discovery.
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spelling pubmed-73817412020-07-27 Mitochondrial Sirtuin 3: New emerging biological function and therapeutic target Zhang, Jin Xiang, Honggang Liu, Jie Chen, Yi He, Rong-Rong Liu, Bo Theranostics Review Sirtuin 3 (SIRT3) is one of the most prominent deacetylases that can regulate acetylation levels in mitochondria, which are essential for eukaryotic life and inextricably linked to the metabolism of multiple organs. Hitherto, SIRT3 has been substantiated to be involved in almost all aspects of mitochondrial metabolism and homeostasis, protecting mitochondria from a variety of damage. Accumulating evidence has recently documented that SIRT3 is associated with many types of human diseases, including age-related diseases, cancer, heart disease and metabolic diseases, indicating that SIRT3 can be a potential therapeutic target. Here we focus on summarizing the intricate mechanisms of SIRT3 in human diseases, and recent notable advances in the field of small-molecule activators or inhibitors targeting SIRT3 as well as their potential therapeutic applications for future drug discovery. Ivyspring International Publisher 2020-07-09 /pmc/articles/PMC7381741/ /pubmed/32724473 http://dx.doi.org/10.7150/thno.45922 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Review
Zhang, Jin
Xiang, Honggang
Liu, Jie
Chen, Yi
He, Rong-Rong
Liu, Bo
Mitochondrial Sirtuin 3: New emerging biological function and therapeutic target
title Mitochondrial Sirtuin 3: New emerging biological function and therapeutic target
title_full Mitochondrial Sirtuin 3: New emerging biological function and therapeutic target
title_fullStr Mitochondrial Sirtuin 3: New emerging biological function and therapeutic target
title_full_unstemmed Mitochondrial Sirtuin 3: New emerging biological function and therapeutic target
title_short Mitochondrial Sirtuin 3: New emerging biological function and therapeutic target
title_sort mitochondrial sirtuin 3: new emerging biological function and therapeutic target
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381741/
https://www.ncbi.nlm.nih.gov/pubmed/32724473
http://dx.doi.org/10.7150/thno.45922
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