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Emerging Therapeutic Potential of SIRT6 Modulators

[Image: see text] Sirtuin 6 (SIRT6) is an NAD(+)-dependent protein deacylase and mono-ADP-ribosyltransferase of the sirtuin family with a wide substrate specificity. In vitro and in vivo studies have indicated that SIRT6 overexpression or activation has beneficial effects for cellular processes such...

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Autores principales: Fiorentino, Francesco, Mai, Antonello, Rotili, Dante
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8389836/
https://www.ncbi.nlm.nih.gov/pubmed/34213345
http://dx.doi.org/10.1021/acs.jmedchem.1c00601
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author Fiorentino, Francesco
Mai, Antonello
Rotili, Dante
author_facet Fiorentino, Francesco
Mai, Antonello
Rotili, Dante
author_sort Fiorentino, Francesco
collection PubMed
description [Image: see text] Sirtuin 6 (SIRT6) is an NAD(+)-dependent protein deacylase and mono-ADP-ribosyltransferase of the sirtuin family with a wide substrate specificity. In vitro and in vivo studies have indicated that SIRT6 overexpression or activation has beneficial effects for cellular processes such as DNA repair, metabolic regulation, and aging. On the other hand, SIRT6 has contrasting roles in cancer, acting either as a tumor suppressor or promoter in a context-specific manner. Given its central role in cellular homeostasis, SIRT6 has emerged as a promising target for the development of small-molecule activators and inhibitors possessing a therapeutic potential in diseases ranging from cancer to age-related disorders. Moreover, specific modulators allow the molecular details of SIRT6 activity to be scrutinized and further validate the enzyme as a pharmacological target. In this Perspective, we summarize the current knowledge about SIRT6 pharmacology and medicinal chemistry and describe the features of the activators and inhibitors identified so far.
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spelling pubmed-83898362021-08-31 Emerging Therapeutic Potential of SIRT6 Modulators Fiorentino, Francesco Mai, Antonello Rotili, Dante J Med Chem [Image: see text] Sirtuin 6 (SIRT6) is an NAD(+)-dependent protein deacylase and mono-ADP-ribosyltransferase of the sirtuin family with a wide substrate specificity. In vitro and in vivo studies have indicated that SIRT6 overexpression or activation has beneficial effects for cellular processes such as DNA repair, metabolic regulation, and aging. On the other hand, SIRT6 has contrasting roles in cancer, acting either as a tumor suppressor or promoter in a context-specific manner. Given its central role in cellular homeostasis, SIRT6 has emerged as a promising target for the development of small-molecule activators and inhibitors possessing a therapeutic potential in diseases ranging from cancer to age-related disorders. Moreover, specific modulators allow the molecular details of SIRT6 activity to be scrutinized and further validate the enzyme as a pharmacological target. In this Perspective, we summarize the current knowledge about SIRT6 pharmacology and medicinal chemistry and describe the features of the activators and inhibitors identified so far. American Chemical Society 2021-07-02 2021-07-22 /pmc/articles/PMC8389836/ /pubmed/34213345 http://dx.doi.org/10.1021/acs.jmedchem.1c00601 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Fiorentino, Francesco
Mai, Antonello
Rotili, Dante
Emerging Therapeutic Potential of SIRT6 Modulators
title Emerging Therapeutic Potential of SIRT6 Modulators
title_full Emerging Therapeutic Potential of SIRT6 Modulators
title_fullStr Emerging Therapeutic Potential of SIRT6 Modulators
title_full_unstemmed Emerging Therapeutic Potential of SIRT6 Modulators
title_short Emerging Therapeutic Potential of SIRT6 Modulators
title_sort emerging therapeutic potential of sirt6 modulators
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8389836/
https://www.ncbi.nlm.nih.gov/pubmed/34213345
http://dx.doi.org/10.1021/acs.jmedchem.1c00601
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