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Regulation of cellular senescence via the FOXO4‐p53 axis

Forkhead box O (FOXO) and p53 proteins are transcription factors that regulate diverse signalling pathways to control cell cycle, apoptosis and metabolism. In the last decade both FOXO and p53 have been identified as key players in aging, and their misregulation is linked to numerous diseases includ...

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Detalles Bibliográficos
Autores principales: Bourgeois, Benjamin, Madl, Tobias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033032/
https://www.ncbi.nlm.nih.gov/pubmed/29683489
http://dx.doi.org/10.1002/1873-3468.13057
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author Bourgeois, Benjamin
Madl, Tobias
author_facet Bourgeois, Benjamin
Madl, Tobias
author_sort Bourgeois, Benjamin
collection PubMed
description Forkhead box O (FOXO) and p53 proteins are transcription factors that regulate diverse signalling pathways to control cell cycle, apoptosis and metabolism. In the last decade both FOXO and p53 have been identified as key players in aging, and their misregulation is linked to numerous diseases including cancers. However, many of the underlying molecular mechanisms remain mysterious, including regulation of ageing by FOXOs and p53. Several activities appear to be shared between FOXOs and p53, including their central role in the regulation of cellular senescence. In this review, we will focus on the recent advances on the link between FOXOs and p53, with a particular focus on the FOXO4‐p53 axis and the role of FOXO4/p53 in cellular senescence. Moreover, we discuss potential strategies for targeting the FOXO4‐p53 interaction to modulate cellular senescence as a drug target in treatment of aging‐related diseases and morbidity.
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spelling pubmed-60330322018-07-12 Regulation of cellular senescence via the FOXO4‐p53 axis Bourgeois, Benjamin Madl, Tobias FEBS Lett Review Articles Forkhead box O (FOXO) and p53 proteins are transcription factors that regulate diverse signalling pathways to control cell cycle, apoptosis and metabolism. In the last decade both FOXO and p53 have been identified as key players in aging, and their misregulation is linked to numerous diseases including cancers. However, many of the underlying molecular mechanisms remain mysterious, including regulation of ageing by FOXOs and p53. Several activities appear to be shared between FOXOs and p53, including their central role in the regulation of cellular senescence. In this review, we will focus on the recent advances on the link between FOXOs and p53, with a particular focus on the FOXO4‐p53 axis and the role of FOXO4/p53 in cellular senescence. Moreover, we discuss potential strategies for targeting the FOXO4‐p53 interaction to modulate cellular senescence as a drug target in treatment of aging‐related diseases and morbidity. John Wiley and Sons Inc. 2018-05-13 2018-06 /pmc/articles/PMC6033032/ /pubmed/29683489 http://dx.doi.org/10.1002/1873-3468.13057 Text en © 2018 The Authors. FEBS Letters published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Articles
Bourgeois, Benjamin
Madl, Tobias
Regulation of cellular senescence via the FOXO4‐p53 axis
title Regulation of cellular senescence via the FOXO4‐p53 axis
title_full Regulation of cellular senescence via the FOXO4‐p53 axis
title_fullStr Regulation of cellular senescence via the FOXO4‐p53 axis
title_full_unstemmed Regulation of cellular senescence via the FOXO4‐p53 axis
title_short Regulation of cellular senescence via the FOXO4‐p53 axis
title_sort regulation of cellular senescence via the foxo4‐p53 axis
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033032/
https://www.ncbi.nlm.nih.gov/pubmed/29683489
http://dx.doi.org/10.1002/1873-3468.13057
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