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HDAC inhibitors in kidney development and disease
The discovery that histone deacetylase inhibitors (HDACis) can attenuate acute kidney injury (AKI)-mediated damage and reduce fibrosis in kidney disease models has opened the possibility of utilizing HDACis as therapeutics for renal injury. Studies to date have made it abundantly clear that HDACi tr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751322/ https://www.ncbi.nlm.nih.gov/pubmed/23052657 http://dx.doi.org/10.1007/s00467-012-2320-8 |
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author | Brilli, Lauren L. Swanhart, Lisa M. de Caestecker, Mark P. Hukriede, Neil A. |
author_facet | Brilli, Lauren L. Swanhart, Lisa M. de Caestecker, Mark P. Hukriede, Neil A. |
author_sort | Brilli, Lauren L. |
collection | PubMed |
description | The discovery that histone deacetylase inhibitors (HDACis) can attenuate acute kidney injury (AKI)-mediated damage and reduce fibrosis in kidney disease models has opened the possibility of utilizing HDACis as therapeutics for renal injury. Studies to date have made it abundantly clear that HDACi treatment results in a plethora of molecular changes, which are not always linked to histone acetylation, and that there is an essential need to understand the specific target(s) of any HDACi of interest. New lines of investigation are beginning to delve more deeply into target identification of specific HDACis and to address the relative toxicity of different HDACi classes. This review will focus on the utilization of HDACis during kidney organogenesis, injury, and disease, as well as on the development of these compounds as therapeutics. |
format | Online Article Text |
id | pubmed-3751322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-37513222013-08-27 HDAC inhibitors in kidney development and disease Brilli, Lauren L. Swanhart, Lisa M. de Caestecker, Mark P. Hukriede, Neil A. Pediatr Nephrol Review The discovery that histone deacetylase inhibitors (HDACis) can attenuate acute kidney injury (AKI)-mediated damage and reduce fibrosis in kidney disease models has opened the possibility of utilizing HDACis as therapeutics for renal injury. Studies to date have made it abundantly clear that HDACi treatment results in a plethora of molecular changes, which are not always linked to histone acetylation, and that there is an essential need to understand the specific target(s) of any HDACi of interest. New lines of investigation are beginning to delve more deeply into target identification of specific HDACis and to address the relative toxicity of different HDACi classes. This review will focus on the utilization of HDACis during kidney organogenesis, injury, and disease, as well as on the development of these compounds as therapeutics. Springer Berlin Heidelberg 2012-10-07 2013 /pmc/articles/PMC3751322/ /pubmed/23052657 http://dx.doi.org/10.1007/s00467-012-2320-8 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Review Brilli, Lauren L. Swanhart, Lisa M. de Caestecker, Mark P. Hukriede, Neil A. HDAC inhibitors in kidney development and disease |
title | HDAC inhibitors in kidney development and disease |
title_full | HDAC inhibitors in kidney development and disease |
title_fullStr | HDAC inhibitors in kidney development and disease |
title_full_unstemmed | HDAC inhibitors in kidney development and disease |
title_short | HDAC inhibitors in kidney development and disease |
title_sort | hdac inhibitors in kidney development and disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751322/ https://www.ncbi.nlm.nih.gov/pubmed/23052657 http://dx.doi.org/10.1007/s00467-012-2320-8 |
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