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Histone deacetylase (HDAC) 9: versatile biological functions and emerging roles in human cancer

BACKGROUND: HDAC9 (histone deacetylase 9) belongs to the class IIa family of histone deacetylases. This enzyme can shuttle freely between the nucleus and cytoplasm and promotes tissue-specific transcriptional regulation by interacting with histone and non-histone substrates. HDAC9 plays an essential...

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Autores principales: Yang, Chun, Croteau, Stéphane, Hardy, Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516780/
https://www.ncbi.nlm.nih.gov/pubmed/34318404
http://dx.doi.org/10.1007/s13402-021-00626-9
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author Yang, Chun
Croteau, Stéphane
Hardy, Pierre
author_facet Yang, Chun
Croteau, Stéphane
Hardy, Pierre
author_sort Yang, Chun
collection PubMed
description BACKGROUND: HDAC9 (histone deacetylase 9) belongs to the class IIa family of histone deacetylases. This enzyme can shuttle freely between the nucleus and cytoplasm and promotes tissue-specific transcriptional regulation by interacting with histone and non-histone substrates. HDAC9 plays an essential role in diverse physiological processes including cardiac muscle development, bone formation, adipocyte differentiation and innate immunity. HDAC9 inhibition or activation is therefore a promising avenue for therapeutic intervention in several diseases. HDAC9 overexpression is also common in cancer cells, where HDAC9 alters the expression and activity of numerous relevant proteins involved in carcinogenesis. CONCLUSIONS: This review summarizes the most recent discoveries regarding HDAC9 as a crucial regulator of specific physiological systems and, more importantly, highlights the diverse spectrum of HDAC9-mediated posttranslational modifications and their contributions to cancer pathogenesis. HDAC9 is a potential novel therapeutic target, and the restoration of aberrant expression patterns observed among HDAC9 target genes and their related signaling pathways may provide opportunities to the design of novel anticancer therapeutic strategies.
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spelling pubmed-85167802021-10-29 Histone deacetylase (HDAC) 9: versatile biological functions and emerging roles in human cancer Yang, Chun Croteau, Stéphane Hardy, Pierre Cell Oncol (Dordr) Review BACKGROUND: HDAC9 (histone deacetylase 9) belongs to the class IIa family of histone deacetylases. This enzyme can shuttle freely between the nucleus and cytoplasm and promotes tissue-specific transcriptional regulation by interacting with histone and non-histone substrates. HDAC9 plays an essential role in diverse physiological processes including cardiac muscle development, bone formation, adipocyte differentiation and innate immunity. HDAC9 inhibition or activation is therefore a promising avenue for therapeutic intervention in several diseases. HDAC9 overexpression is also common in cancer cells, where HDAC9 alters the expression and activity of numerous relevant proteins involved in carcinogenesis. CONCLUSIONS: This review summarizes the most recent discoveries regarding HDAC9 as a crucial regulator of specific physiological systems and, more importantly, highlights the diverse spectrum of HDAC9-mediated posttranslational modifications and their contributions to cancer pathogenesis. HDAC9 is a potential novel therapeutic target, and the restoration of aberrant expression patterns observed among HDAC9 target genes and their related signaling pathways may provide opportunities to the design of novel anticancer therapeutic strategies. Springer Netherlands 2021-07-27 2021 /pmc/articles/PMC8516780/ /pubmed/34318404 http://dx.doi.org/10.1007/s13402-021-00626-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review
Yang, Chun
Croteau, Stéphane
Hardy, Pierre
Histone deacetylase (HDAC) 9: versatile biological functions and emerging roles in human cancer
title Histone deacetylase (HDAC) 9: versatile biological functions and emerging roles in human cancer
title_full Histone deacetylase (HDAC) 9: versatile biological functions and emerging roles in human cancer
title_fullStr Histone deacetylase (HDAC) 9: versatile biological functions and emerging roles in human cancer
title_full_unstemmed Histone deacetylase (HDAC) 9: versatile biological functions and emerging roles in human cancer
title_short Histone deacetylase (HDAC) 9: versatile biological functions and emerging roles in human cancer
title_sort histone deacetylase (hdac) 9: versatile biological functions and emerging roles in human cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516780/
https://www.ncbi.nlm.nih.gov/pubmed/34318404
http://dx.doi.org/10.1007/s13402-021-00626-9
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