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The SIRT1-c-Myc axis in regulation of stem cells

SIRT1 is the most conserved mammalian NAD(+)-dependent protein deacetylase. Through deacetylation of transcriptional factors and co-factors, this protein modification enzyme is critically involved in metabolic and epigenetic regulation of stem cells, which is functionally important in maintaining th...

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Detalles Bibliográficos
Autores principales: Fan, Wei, Li, Xiaoling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10405831/
https://www.ncbi.nlm.nih.gov/pubmed/37554307
http://dx.doi.org/10.3389/fcell.2023.1236968
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author Fan, Wei
Li, Xiaoling
author_facet Fan, Wei
Li, Xiaoling
author_sort Fan, Wei
collection PubMed
description SIRT1 is the most conserved mammalian NAD(+)-dependent protein deacetylase. Through deacetylation of transcriptional factors and co-factors, this protein modification enzyme is critically involved in metabolic and epigenetic regulation of stem cells, which is functionally important in maintaining their pluripotency and regulating their differentiation. C-Myc, a key member of Myc proton-oncogene family, is a pivotal factor for transcriptional regulation of genes that control acquisition and maintenance of stemness. Previous cancer research has revealed an intriguing positive feedback loop between SIRT1 and c-Myc that is crucial in tumorigenesis. Recent literature has uncovered important functions of this axis in regulation of maintenance and differentiation of stem cells, including pluripotent stem cells and cancer stem cells. This review highlights recent advances of the SIRT1-c-Myc axis in stem cells.
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spelling pubmed-104058312023-08-08 The SIRT1-c-Myc axis in regulation of stem cells Fan, Wei Li, Xiaoling Front Cell Dev Biol Cell and Developmental Biology SIRT1 is the most conserved mammalian NAD(+)-dependent protein deacetylase. Through deacetylation of transcriptional factors and co-factors, this protein modification enzyme is critically involved in metabolic and epigenetic regulation of stem cells, which is functionally important in maintaining their pluripotency and regulating their differentiation. C-Myc, a key member of Myc proton-oncogene family, is a pivotal factor for transcriptional regulation of genes that control acquisition and maintenance of stemness. Previous cancer research has revealed an intriguing positive feedback loop between SIRT1 and c-Myc that is crucial in tumorigenesis. Recent literature has uncovered important functions of this axis in regulation of maintenance and differentiation of stem cells, including pluripotent stem cells and cancer stem cells. This review highlights recent advances of the SIRT1-c-Myc axis in stem cells. Frontiers Media S.A. 2023-07-24 /pmc/articles/PMC10405831/ /pubmed/37554307 http://dx.doi.org/10.3389/fcell.2023.1236968 Text en Copyright © 2023 Fan and Li. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Fan, Wei
Li, Xiaoling
The SIRT1-c-Myc axis in regulation of stem cells
title The SIRT1-c-Myc axis in regulation of stem cells
title_full The SIRT1-c-Myc axis in regulation of stem cells
title_fullStr The SIRT1-c-Myc axis in regulation of stem cells
title_full_unstemmed The SIRT1-c-Myc axis in regulation of stem cells
title_short The SIRT1-c-Myc axis in regulation of stem cells
title_sort sirt1-c-myc axis in regulation of stem cells
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10405831/
https://www.ncbi.nlm.nih.gov/pubmed/37554307
http://dx.doi.org/10.3389/fcell.2023.1236968
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