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HDAC6—An Emerging Target Against Chronic Myeloid Leukemia?

Imatinib became the standard treatment for chronic myeloid leukemia (CML) about 20 years ago, which was a major breakthrough in stabilizing the pathology and improving the quality of life of patients. However, the emergence of resistance to imatinib and other tyrosine kinase inhibitors leads researc...

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Autores principales: Losson, Hélène, Schnekenburger, Michael, Dicato, Mario, Diederich, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072136/
https://www.ncbi.nlm.nih.gov/pubmed/32013157
http://dx.doi.org/10.3390/cancers12020318
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author Losson, Hélène
Schnekenburger, Michael
Dicato, Mario
Diederich, Marc
author_facet Losson, Hélène
Schnekenburger, Michael
Dicato, Mario
Diederich, Marc
author_sort Losson, Hélène
collection PubMed
description Imatinib became the standard treatment for chronic myeloid leukemia (CML) about 20 years ago, which was a major breakthrough in stabilizing the pathology and improving the quality of life of patients. However, the emergence of resistance to imatinib and other tyrosine kinase inhibitors leads researchers to characterize new therapeutic targets. Several studies have highlighted the role of histone deacetylase 6 (HDAC6) in various pathologies, including cancer. This protein effectively intervenes in cellular activities by its primarily cytoplasmic localization. In this review, we will discuss the molecular characteristics of the HDAC6 protein, as well as its overexpression in CML leukemic stem cells, which make it a promising therapeutic target for the treatment of CML.
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spelling pubmed-70721362020-03-19 HDAC6—An Emerging Target Against Chronic Myeloid Leukemia? Losson, Hélène Schnekenburger, Michael Dicato, Mario Diederich, Marc Cancers (Basel) Review Imatinib became the standard treatment for chronic myeloid leukemia (CML) about 20 years ago, which was a major breakthrough in stabilizing the pathology and improving the quality of life of patients. However, the emergence of resistance to imatinib and other tyrosine kinase inhibitors leads researchers to characterize new therapeutic targets. Several studies have highlighted the role of histone deacetylase 6 (HDAC6) in various pathologies, including cancer. This protein effectively intervenes in cellular activities by its primarily cytoplasmic localization. In this review, we will discuss the molecular characteristics of the HDAC6 protein, as well as its overexpression in CML leukemic stem cells, which make it a promising therapeutic target for the treatment of CML. MDPI 2020-01-29 /pmc/articles/PMC7072136/ /pubmed/32013157 http://dx.doi.org/10.3390/cancers12020318 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Losson, Hélène
Schnekenburger, Michael
Dicato, Mario
Diederich, Marc
HDAC6—An Emerging Target Against Chronic Myeloid Leukemia?
title HDAC6—An Emerging Target Against Chronic Myeloid Leukemia?
title_full HDAC6—An Emerging Target Against Chronic Myeloid Leukemia?
title_fullStr HDAC6—An Emerging Target Against Chronic Myeloid Leukemia?
title_full_unstemmed HDAC6—An Emerging Target Against Chronic Myeloid Leukemia?
title_short HDAC6—An Emerging Target Against Chronic Myeloid Leukemia?
title_sort hdac6—an emerging target against chronic myeloid leukemia?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072136/
https://www.ncbi.nlm.nih.gov/pubmed/32013157
http://dx.doi.org/10.3390/cancers12020318
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