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A c-Myc–SIRT1 feedback loop regulates cell growth and transformation

The protein deacetylase SIRT1 has been implicated in a variety of cellular functions, including development, cellular stress responses, and metabolism. Increasing evidence suggests that similar to its counterpart, Sir2, in yeast, Caenorhabditis elegans, and Drosophila melanogaster, SIRT1 may functio...

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Detalles Bibliográficos
Autores principales: Yuan, Jian, Minter-Dykhouse, Katherine, Lou, Zhenkun
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2700370/
https://www.ncbi.nlm.nih.gov/pubmed/19364925
http://dx.doi.org/10.1083/jcb.200809167
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author Yuan, Jian
Minter-Dykhouse, Katherine
Lou, Zhenkun
author_facet Yuan, Jian
Minter-Dykhouse, Katherine
Lou, Zhenkun
author_sort Yuan, Jian
collection PubMed
description The protein deacetylase SIRT1 has been implicated in a variety of cellular functions, including development, cellular stress responses, and metabolism. Increasing evidence suggests that similar to its counterpart, Sir2, in yeast, Caenorhabditis elegans, and Drosophila melanogaster, SIRT1 may function to regulate life span in mammals. However, SIRT1's role in cancer is unclear. During our investigation of SIRT1, we found that c-Myc binds to the SIRT1 promoter and induces SIRT1 expression. However, SIRT1 interacts with and deacetylates c-Myc, resulting in decreased c-Myc stability. As a consequence, c-Myc's transformational capability is compromised in the presence of SIRT1. Overall, our experiments identify a c-Myc–SIRT1 feedback loop in the regulation of c-Myc activity and cellular transformation, supporting/suggesting a role of SIRT1 in tumor suppression.
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spelling pubmed-27003702009-10-20 A c-Myc–SIRT1 feedback loop regulates cell growth and transformation Yuan, Jian Minter-Dykhouse, Katherine Lou, Zhenkun J Cell Biol Research Articles The protein deacetylase SIRT1 has been implicated in a variety of cellular functions, including development, cellular stress responses, and metabolism. Increasing evidence suggests that similar to its counterpart, Sir2, in yeast, Caenorhabditis elegans, and Drosophila melanogaster, SIRT1 may function to regulate life span in mammals. However, SIRT1's role in cancer is unclear. During our investigation of SIRT1, we found that c-Myc binds to the SIRT1 promoter and induces SIRT1 expression. However, SIRT1 interacts with and deacetylates c-Myc, resulting in decreased c-Myc stability. As a consequence, c-Myc's transformational capability is compromised in the presence of SIRT1. Overall, our experiments identify a c-Myc–SIRT1 feedback loop in the regulation of c-Myc activity and cellular transformation, supporting/suggesting a role of SIRT1 in tumor suppression. The Rockefeller University Press 2009-04-20 /pmc/articles/PMC2700370/ /pubmed/19364925 http://dx.doi.org/10.1083/jcb.200809167 Text en © 2009 Yuan et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Yuan, Jian
Minter-Dykhouse, Katherine
Lou, Zhenkun
A c-Myc–SIRT1 feedback loop regulates cell growth and transformation
title A c-Myc–SIRT1 feedback loop regulates cell growth and transformation
title_full A c-Myc–SIRT1 feedback loop regulates cell growth and transformation
title_fullStr A c-Myc–SIRT1 feedback loop regulates cell growth and transformation
title_full_unstemmed A c-Myc–SIRT1 feedback loop regulates cell growth and transformation
title_short A c-Myc–SIRT1 feedback loop regulates cell growth and transformation
title_sort c-myc–sirt1 feedback loop regulates cell growth and transformation
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2700370/
https://www.ncbi.nlm.nih.gov/pubmed/19364925
http://dx.doi.org/10.1083/jcb.200809167
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