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SIRT2 as a Therapeutic Target for Age-Related Disorders

Sirtuin proteins are conserved regulators of aging that have recently emerged as important modifiers of several diseases which commonly occur later in life such as cancer, diabetes, cardiovascular, and neurodegenerative diseases. In mammals, there are seven sirtuins (SIRT1-7), which display diversit...

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Autores principales: de Oliveira, Rita Machado, Sarkander, Jana, Kazantsev, Aleksey G., Outeiro, Tiago Fleming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342661/
https://www.ncbi.nlm.nih.gov/pubmed/22563317
http://dx.doi.org/10.3389/fphar.2012.00082
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author de Oliveira, Rita Machado
Sarkander, Jana
Kazantsev, Aleksey G.
Outeiro, Tiago Fleming
author_facet de Oliveira, Rita Machado
Sarkander, Jana
Kazantsev, Aleksey G.
Outeiro, Tiago Fleming
author_sort de Oliveira, Rita Machado
collection PubMed
description Sirtuin proteins are conserved regulators of aging that have recently emerged as important modifiers of several diseases which commonly occur later in life such as cancer, diabetes, cardiovascular, and neurodegenerative diseases. In mammals, there are seven sirtuins (SIRT1-7), which display diversity in subcellular localization and function. SIRT1 has received much of attention due to its possible impact on longevity, while important biological and therapeutic roles of other sirtuins have been underestimated and just recently recognized. Here we focus on SIRT2, a member of the sirtuin family, and discuss its role in cellular and tissue-specific functions. This review summarizes the main scientific advances on SIRT2 protein biology and explores its potential as a therapeutic target for treatment of age-related disorders.
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spelling pubmed-33426612012-05-04 SIRT2 as a Therapeutic Target for Age-Related Disorders de Oliveira, Rita Machado Sarkander, Jana Kazantsev, Aleksey G. Outeiro, Tiago Fleming Front Pharmacol Pharmacology Sirtuin proteins are conserved regulators of aging that have recently emerged as important modifiers of several diseases which commonly occur later in life such as cancer, diabetes, cardiovascular, and neurodegenerative diseases. In mammals, there are seven sirtuins (SIRT1-7), which display diversity in subcellular localization and function. SIRT1 has received much of attention due to its possible impact on longevity, while important biological and therapeutic roles of other sirtuins have been underestimated and just recently recognized. Here we focus on SIRT2, a member of the sirtuin family, and discuss its role in cellular and tissue-specific functions. This review summarizes the main scientific advances on SIRT2 protein biology and explores its potential as a therapeutic target for treatment of age-related disorders. Frontiers Research Foundation 2012-05-03 /pmc/articles/PMC3342661/ /pubmed/22563317 http://dx.doi.org/10.3389/fphar.2012.00082 Text en Copyright © 2012 de Oliveira, Sarkander, Kazantsev and Outeiro. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Pharmacology
de Oliveira, Rita Machado
Sarkander, Jana
Kazantsev, Aleksey G.
Outeiro, Tiago Fleming
SIRT2 as a Therapeutic Target for Age-Related Disorders
title SIRT2 as a Therapeutic Target for Age-Related Disorders
title_full SIRT2 as a Therapeutic Target for Age-Related Disorders
title_fullStr SIRT2 as a Therapeutic Target for Age-Related Disorders
title_full_unstemmed SIRT2 as a Therapeutic Target for Age-Related Disorders
title_short SIRT2 as a Therapeutic Target for Age-Related Disorders
title_sort sirt2 as a therapeutic target for age-related disorders
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342661/
https://www.ncbi.nlm.nih.gov/pubmed/22563317
http://dx.doi.org/10.3389/fphar.2012.00082
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