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Pathological Role of HDAC8: Cancer and Beyond

Histone deacetylase 8 (HDAC8) is a class I HDAC that catalyzes the deacetylation of histone and non-histone proteins. As one of the best-characterized isoforms, numerous studies have identified interacting partners of HDAC8 pertaining to diverse molecular mechanisms. Consequently, deregulation and o...

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Autores principales: Kim, Ji Yoon, Cho, Hayoung, Yoo, Jung, Kim, Go Woon, Jeon, Yu Hyun, Lee, Sang Wu, Kwon, So Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563588/
https://www.ncbi.nlm.nih.gov/pubmed/36231123
http://dx.doi.org/10.3390/cells11193161
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author Kim, Ji Yoon
Cho, Hayoung
Yoo, Jung
Kim, Go Woon
Jeon, Yu Hyun
Lee, Sang Wu
Kwon, So Hee
author_facet Kim, Ji Yoon
Cho, Hayoung
Yoo, Jung
Kim, Go Woon
Jeon, Yu Hyun
Lee, Sang Wu
Kwon, So Hee
author_sort Kim, Ji Yoon
collection PubMed
description Histone deacetylase 8 (HDAC8) is a class I HDAC that catalyzes the deacetylation of histone and non-histone proteins. As one of the best-characterized isoforms, numerous studies have identified interacting partners of HDAC8 pertaining to diverse molecular mechanisms. Consequently, deregulation and overexpression of HDAC8 give rise to diseases. HDAC8 is especially involved in various aspects of cancer progression, such as cancer cell proliferation, metastasis, immune evasion, and drug resistance. HDAC8 is also associated with the development of non-cancer diseases such as Cornelia de Lange Syndrome (CdLS), infectious diseases, cardiovascular diseases, pulmonary diseases, and myopathy. Therefore, HDAC8 is an attractive therapeutic target and various HDAC8 selective inhibitors (HDAC8is) have been developed. Here, we address the pathological function of HDAC8 in cancer and other diseases, as well as illustrate several HDAC8is that have shown anti-cancer effects.
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spelling pubmed-95635882022-10-15 Pathological Role of HDAC8: Cancer and Beyond Kim, Ji Yoon Cho, Hayoung Yoo, Jung Kim, Go Woon Jeon, Yu Hyun Lee, Sang Wu Kwon, So Hee Cells Review Histone deacetylase 8 (HDAC8) is a class I HDAC that catalyzes the deacetylation of histone and non-histone proteins. As one of the best-characterized isoforms, numerous studies have identified interacting partners of HDAC8 pertaining to diverse molecular mechanisms. Consequently, deregulation and overexpression of HDAC8 give rise to diseases. HDAC8 is especially involved in various aspects of cancer progression, such as cancer cell proliferation, metastasis, immune evasion, and drug resistance. HDAC8 is also associated with the development of non-cancer diseases such as Cornelia de Lange Syndrome (CdLS), infectious diseases, cardiovascular diseases, pulmonary diseases, and myopathy. Therefore, HDAC8 is an attractive therapeutic target and various HDAC8 selective inhibitors (HDAC8is) have been developed. Here, we address the pathological function of HDAC8 in cancer and other diseases, as well as illustrate several HDAC8is that have shown anti-cancer effects. MDPI 2022-10-09 /pmc/articles/PMC9563588/ /pubmed/36231123 http://dx.doi.org/10.3390/cells11193161 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
Kim, Ji Yoon
Cho, Hayoung
Yoo, Jung
Kim, Go Woon
Jeon, Yu Hyun
Lee, Sang Wu
Kwon, So Hee
Pathological Role of HDAC8: Cancer and Beyond
title Pathological Role of HDAC8: Cancer and Beyond
title_full Pathological Role of HDAC8: Cancer and Beyond
title_fullStr Pathological Role of HDAC8: Cancer and Beyond
title_full_unstemmed Pathological Role of HDAC8: Cancer and Beyond
title_short Pathological Role of HDAC8: Cancer and Beyond
title_sort pathological role of hdac8: cancer and beyond
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563588/
https://www.ncbi.nlm.nih.gov/pubmed/36231123
http://dx.doi.org/10.3390/cells11193161
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