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Histone deacetylase inhibitors as potential treatment for spinal muscular atrophy
Histone acetylation plays an important role in regulation of transcription in eukaryotic cells by promoting a more relaxed chromatin structure necessary for transcriptional activation. Histone deacetylases (HDACs) remove acetyl groups and suppress gene expression. HDAC inhibitors (HDACIs) are a grou...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Genética
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3795173/ https://www.ncbi.nlm.nih.gov/pubmed/24130434 http://dx.doi.org/10.1590/S1415-47572013000300001 |
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author | Mohseni, Jafar Zabidi-Hussin, Z.A.M.H. Sasongko, Teguh Haryo |
author_facet | Mohseni, Jafar Zabidi-Hussin, Z.A.M.H. Sasongko, Teguh Haryo |
author_sort | Mohseni, Jafar |
collection | PubMed |
description | Histone acetylation plays an important role in regulation of transcription in eukaryotic cells by promoting a more relaxed chromatin structure necessary for transcriptional activation. Histone deacetylases (HDACs) remove acetyl groups and suppress gene expression. HDAC inhibitors (HDACIs) are a group of small molecules that promote gene transcription by chromatin remodeling and have been extensively studied as potential drugs for treating of spinal muscular atrophy. Various drugs in this class have been studied with regard to their efficacy in increasing the expression of survival of motor neuron (SMN) protein. In this review, we discuss the current literature on this topic and summarize the findings of the main studies in this field. |
format | Online Article Text |
id | pubmed-3795173 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Sociedade Brasileira de Genética |
record_format | MEDLINE/PubMed |
spelling | pubmed-37951732013-10-15 Histone deacetylase inhibitors as potential treatment for spinal muscular atrophy Mohseni, Jafar Zabidi-Hussin, Z.A.M.H. Sasongko, Teguh Haryo Genet Mol Biol Review Article Histone acetylation plays an important role in regulation of transcription in eukaryotic cells by promoting a more relaxed chromatin structure necessary for transcriptional activation. Histone deacetylases (HDACs) remove acetyl groups and suppress gene expression. HDAC inhibitors (HDACIs) are a group of small molecules that promote gene transcription by chromatin remodeling and have been extensively studied as potential drugs for treating of spinal muscular atrophy. Various drugs in this class have been studied with regard to their efficacy in increasing the expression of survival of motor neuron (SMN) protein. In this review, we discuss the current literature on this topic and summarize the findings of the main studies in this field. Sociedade Brasileira de Genética 2013-09 2013-08-30 /pmc/articles/PMC3795173/ /pubmed/24130434 http://dx.doi.org/10.1590/S1415-47572013000300001 Text en Copyright © 2013, Sociedade Brasileira de Genética. License information: 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 work is properly cited. |
spellingShingle | Review Article Mohseni, Jafar Zabidi-Hussin, Z.A.M.H. Sasongko, Teguh Haryo Histone deacetylase inhibitors as potential treatment for spinal muscular atrophy |
title | Histone deacetylase inhibitors as potential treatment for spinal muscular atrophy |
title_full | Histone deacetylase inhibitors as potential treatment for spinal muscular atrophy |
title_fullStr | Histone deacetylase inhibitors as potential treatment for spinal muscular atrophy |
title_full_unstemmed | Histone deacetylase inhibitors as potential treatment for spinal muscular atrophy |
title_short | Histone deacetylase inhibitors as potential treatment for spinal muscular atrophy |
title_sort | histone deacetylase inhibitors as potential treatment for spinal muscular atrophy |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3795173/ https://www.ncbi.nlm.nih.gov/pubmed/24130434 http://dx.doi.org/10.1590/S1415-47572013000300001 |
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