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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...

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Detalles Bibliográficos
Autores principales: Brilli, Lauren L., Swanhart, Lisa M., de Caestecker, Mark P., Hukriede, Neil A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2012
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.
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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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