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Epigenetic Regulation of Cellular Senescence

Senescence is a complex cellular stress response that abolishes proliferative capacity and generates a unique secretory pattern that is implicated in organismal aging and age-related disease. How a cell transitions to a senescent state is multifactorial and often requires transcriptional regulation...

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Autores principales: Crouch, Jack, Shvedova, Maria, Thanapaul, Rex Jeya Rajkumar Samdavid, Botchkarev, Vladimir, Roh, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8870565/
https://www.ncbi.nlm.nih.gov/pubmed/35203320
http://dx.doi.org/10.3390/cells11040672
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author Crouch, Jack
Shvedova, Maria
Thanapaul, Rex Jeya Rajkumar Samdavid
Botchkarev, Vladimir
Roh, Daniel
author_facet Crouch, Jack
Shvedova, Maria
Thanapaul, Rex Jeya Rajkumar Samdavid
Botchkarev, Vladimir
Roh, Daniel
author_sort Crouch, Jack
collection PubMed
description Senescence is a complex cellular stress response that abolishes proliferative capacity and generates a unique secretory pattern that is implicated in organismal aging and age-related disease. How a cell transitions to a senescent state is multifactorial and often requires transcriptional regulation of multiple genes. Epigenetic alterations to DNA and chromatin are powerful regulators of genome architecture and gene expression, and they play a crucial role in mediating the induction and maintenance of senescence. This review will highlight the changes in chromatin, DNA methylation, and histone alterations that establish and maintain cellular senescence, alongside the specific epigenetic regulation of the senescence-associated secretory phenotype (SASP).
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spelling pubmed-88705652022-02-25 Epigenetic Regulation of Cellular Senescence Crouch, Jack Shvedova, Maria Thanapaul, Rex Jeya Rajkumar Samdavid Botchkarev, Vladimir Roh, Daniel Cells Review Senescence is a complex cellular stress response that abolishes proliferative capacity and generates a unique secretory pattern that is implicated in organismal aging and age-related disease. How a cell transitions to a senescent state is multifactorial and often requires transcriptional regulation of multiple genes. Epigenetic alterations to DNA and chromatin are powerful regulators of genome architecture and gene expression, and they play a crucial role in mediating the induction and maintenance of senescence. This review will highlight the changes in chromatin, DNA methylation, and histone alterations that establish and maintain cellular senescence, alongside the specific epigenetic regulation of the senescence-associated secretory phenotype (SASP). MDPI 2022-02-15 /pmc/articles/PMC8870565/ /pubmed/35203320 http://dx.doi.org/10.3390/cells11040672 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Crouch, Jack
Shvedova, Maria
Thanapaul, Rex Jeya Rajkumar Samdavid
Botchkarev, Vladimir
Roh, Daniel
Epigenetic Regulation of Cellular Senescence
title Epigenetic Regulation of Cellular Senescence
title_full Epigenetic Regulation of Cellular Senescence
title_fullStr Epigenetic Regulation of Cellular Senescence
title_full_unstemmed Epigenetic Regulation of Cellular Senescence
title_short Epigenetic Regulation of Cellular Senescence
title_sort epigenetic regulation of cellular senescence
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8870565/
https://www.ncbi.nlm.nih.gov/pubmed/35203320
http://dx.doi.org/10.3390/cells11040672
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