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Epigenetic regulation in adult stem cells and cancers

Adult stem cells maintain tissue homeostasis by their ability to both self-renew and differentiate to distinct cell types. Multiple signaling pathways have been shown to play essential roles as extrinsic cues in maintaining adult stem cell identity and activity. Recent studies also show dynamic regu...

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Detalles Bibliográficos
Autores principales: Tarayrah, Lama, Chen, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852361/
https://www.ncbi.nlm.nih.gov/pubmed/24172544
http://dx.doi.org/10.1186/2045-3701-3-41
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author Tarayrah, Lama
Chen, Xin
author_facet Tarayrah, Lama
Chen, Xin
author_sort Tarayrah, Lama
collection PubMed
description Adult stem cells maintain tissue homeostasis by their ability to both self-renew and differentiate to distinct cell types. Multiple signaling pathways have been shown to play essential roles as extrinsic cues in maintaining adult stem cell identity and activity. Recent studies also show dynamic regulation by epigenetic mechanisms as intrinsic factors in multiple adult stem cell lineages. Emerging evidence demonstrates intimate crosstalk between these two mechanisms. Misregulation of adult stem cell activity could lead to tumorigenesis, and it has been proposed that cancer stem cells may be responsible for tumor growth and metastasis. However, it is unclear whether cancer stem cells share commonalities with normal adult stem cells. In this review, we will focus on recent discoveries of epigenetic regulation in multiple adult stem cell lineages. We will also discuss how epigenetic mechanisms regulate cancer stem cell activity and probe the common and different features between cancer stem cells and normal adult stem cells.
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spelling pubmed-38523612013-12-06 Epigenetic regulation in adult stem cells and cancers Tarayrah, Lama Chen, Xin Cell Biosci Review Adult stem cells maintain tissue homeostasis by their ability to both self-renew and differentiate to distinct cell types. Multiple signaling pathways have been shown to play essential roles as extrinsic cues in maintaining adult stem cell identity and activity. Recent studies also show dynamic regulation by epigenetic mechanisms as intrinsic factors in multiple adult stem cell lineages. Emerging evidence demonstrates intimate crosstalk between these two mechanisms. Misregulation of adult stem cell activity could lead to tumorigenesis, and it has been proposed that cancer stem cells may be responsible for tumor growth and metastasis. However, it is unclear whether cancer stem cells share commonalities with normal adult stem cells. In this review, we will focus on recent discoveries of epigenetic regulation in multiple adult stem cell lineages. We will also discuss how epigenetic mechanisms regulate cancer stem cell activity and probe the common and different features between cancer stem cells and normal adult stem cells. BioMed Central 2013-10-09 /pmc/articles/PMC3852361/ /pubmed/24172544 http://dx.doi.org/10.1186/2045-3701-3-41 Text en Copyright © 2013 Tarayrah and Chen; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Tarayrah, Lama
Chen, Xin
Epigenetic regulation in adult stem cells and cancers
title Epigenetic regulation in adult stem cells and cancers
title_full Epigenetic regulation in adult stem cells and cancers
title_fullStr Epigenetic regulation in adult stem cells and cancers
title_full_unstemmed Epigenetic regulation in adult stem cells and cancers
title_short Epigenetic regulation in adult stem cells and cancers
title_sort epigenetic regulation in adult stem cells and cancers
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852361/
https://www.ncbi.nlm.nih.gov/pubmed/24172544
http://dx.doi.org/10.1186/2045-3701-3-41
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