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Autophagic and Apoptotic Effects of HDAC Inhibitors on Cancer Cells

Because epigenetic alterations are believed to be involved in the repression of tumor suppressor genes and the promotion of tumorigenesis in cancers, novel compounds endowed with histone deacetylase (HDAC) inhibitory activity are an attractive therapeutic approach. Indeed, the potential of HDAC inhi...

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Detalles Bibliográficos
Autor principal: Rikiishi, Hidemi
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3100649/
https://www.ncbi.nlm.nih.gov/pubmed/21629704
http://dx.doi.org/10.1155/2011/830260
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author Rikiishi, Hidemi
author_facet Rikiishi, Hidemi
author_sort Rikiishi, Hidemi
collection PubMed
description Because epigenetic alterations are believed to be involved in the repression of tumor suppressor genes and the promotion of tumorigenesis in cancers, novel compounds endowed with histone deacetylase (HDAC) inhibitory activity are an attractive therapeutic approach. Indeed, the potential of HDAC inhibitors for cancer therapy has been explored in preclinical models, and some agents approved for hematologic malignancies have reached the clinical setting. HDAC inhibitors are able to mediate the induction of both apoptosis and autophagy, which are related to anticancer activity in a variety of cancer cell lines. Given the inherent resistance to apoptosis that characterizes cancer, the targeting of alternative pathways is an attractive strategy to improve anti-tumor therapy. The activation of autophagy represents novel cancer treatment targets. This paper aims to critically discuss how the anticancer potential of HDAC inhibitors may elicit a response to human cancers through different cell pathways leading to cell death.
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spelling pubmed-31006492011-05-31 Autophagic and Apoptotic Effects of HDAC Inhibitors on Cancer Cells Rikiishi, Hidemi J Biomed Biotechnol Review Article Because epigenetic alterations are believed to be involved in the repression of tumor suppressor genes and the promotion of tumorigenesis in cancers, novel compounds endowed with histone deacetylase (HDAC) inhibitory activity are an attractive therapeutic approach. Indeed, the potential of HDAC inhibitors for cancer therapy has been explored in preclinical models, and some agents approved for hematologic malignancies have reached the clinical setting. HDAC inhibitors are able to mediate the induction of both apoptosis and autophagy, which are related to anticancer activity in a variety of cancer cell lines. Given the inherent resistance to apoptosis that characterizes cancer, the targeting of alternative pathways is an attractive strategy to improve anti-tumor therapy. The activation of autophagy represents novel cancer treatment targets. This paper aims to critically discuss how the anticancer potential of HDAC inhibitors may elicit a response to human cancers through different cell pathways leading to cell death. Hindawi Publishing Corporation 2011 2011-05-18 /pmc/articles/PMC3100649/ /pubmed/21629704 http://dx.doi.org/10.1155/2011/830260 Text en Copyright © 2011 Hidemi Rikiishi. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Rikiishi, Hidemi
Autophagic and Apoptotic Effects of HDAC Inhibitors on Cancer Cells
title Autophagic and Apoptotic Effects of HDAC Inhibitors on Cancer Cells
title_full Autophagic and Apoptotic Effects of HDAC Inhibitors on Cancer Cells
title_fullStr Autophagic and Apoptotic Effects of HDAC Inhibitors on Cancer Cells
title_full_unstemmed Autophagic and Apoptotic Effects of HDAC Inhibitors on Cancer Cells
title_short Autophagic and Apoptotic Effects of HDAC Inhibitors on Cancer Cells
title_sort autophagic and apoptotic effects of hdac inhibitors on cancer cells
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3100649/
https://www.ncbi.nlm.nih.gov/pubmed/21629704
http://dx.doi.org/10.1155/2011/830260
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