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Advances in epigenetic glioblastoma therapy

Glioblastoma multiforme (GBM) is the most lethal primary brain tumor in adults despite contemporary gold-standard first-line treatment strategies. This type of tumor recurs in virtually all patients and no commonly accepted standard treatment exists for the recurrent disease. Therefore, advances in...

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Autores principales: Lee, Dong Hoon, Ryu, Hyun-Wook, Won, Hye-Rim, Kwon, So Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5392350/
https://www.ncbi.nlm.nih.gov/pubmed/28099914
http://dx.doi.org/10.18632/oncotarget.14612
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author Lee, Dong Hoon
Ryu, Hyun-Wook
Won, Hye-Rim
Kwon, So Hee
author_facet Lee, Dong Hoon
Ryu, Hyun-Wook
Won, Hye-Rim
Kwon, So Hee
author_sort Lee, Dong Hoon
collection PubMed
description Glioblastoma multiforme (GBM) is the most lethal primary brain tumor in adults despite contemporary gold-standard first-line treatment strategies. This type of tumor recurs in virtually all patients and no commonly accepted standard treatment exists for the recurrent disease. Therefore, advances in all scientific and clinical aspects of GBM are urgently needed. Epigenetic mechanisms are one of the major factors contributing to the pathogenesis of cancers, including glioblastoma. Epigenetic modulators that regulate gene expression by altering the epigenome and non-histone proteins are being exploited as therapeutic drug targets. Over the last decade, numerous preclinical and clinical studies on histone deacetylase (HDAC) inhibitors have shown promising results in various cancers. This article provides an overview of the anticancer mechanisms of HDAC inhibitors and the role of HDAC isoforms in GBM. We also summarize current knowledge on HDAC inhibitors on the basis of preclinical studies and emerging clinical data.
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spelling pubmed-53923502017-04-21 Advances in epigenetic glioblastoma therapy Lee, Dong Hoon Ryu, Hyun-Wook Won, Hye-Rim Kwon, So Hee Oncotarget Review Glioblastoma multiforme (GBM) is the most lethal primary brain tumor in adults despite contemporary gold-standard first-line treatment strategies. This type of tumor recurs in virtually all patients and no commonly accepted standard treatment exists for the recurrent disease. Therefore, advances in all scientific and clinical aspects of GBM are urgently needed. Epigenetic mechanisms are one of the major factors contributing to the pathogenesis of cancers, including glioblastoma. Epigenetic modulators that regulate gene expression by altering the epigenome and non-histone proteins are being exploited as therapeutic drug targets. Over the last decade, numerous preclinical and clinical studies on histone deacetylase (HDAC) inhibitors have shown promising results in various cancers. This article provides an overview of the anticancer mechanisms of HDAC inhibitors and the role of HDAC isoforms in GBM. We also summarize current knowledge on HDAC inhibitors on the basis of preclinical studies and emerging clinical data. Impact Journals LLC 2017-01-12 /pmc/articles/PMC5392350/ /pubmed/28099914 http://dx.doi.org/10.18632/oncotarget.14612 Text en Copyright: © 2017 Lee et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Review
Lee, Dong Hoon
Ryu, Hyun-Wook
Won, Hye-Rim
Kwon, So Hee
Advances in epigenetic glioblastoma therapy
title Advances in epigenetic glioblastoma therapy
title_full Advances in epigenetic glioblastoma therapy
title_fullStr Advances in epigenetic glioblastoma therapy
title_full_unstemmed Advances in epigenetic glioblastoma therapy
title_short Advances in epigenetic glioblastoma therapy
title_sort advances in epigenetic glioblastoma therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5392350/
https://www.ncbi.nlm.nih.gov/pubmed/28099914
http://dx.doi.org/10.18632/oncotarget.14612
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