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Long non-coding RNA-H19 antagonism protects against renal fibrosis

Although long non-coding RNAs (lncRNAs) are important players in the initiation and progression of many pathological processes, the role of lncRNAs in renal fibrosis still remains unclear. We showed that lncRNA-H19 expression was significantly up-regulated in TGF-β2-induced HK-2 cell fibrosis and un...

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Autores principales: Xie, Hong, Xue, Jing-Dong, Chao, Feng, Jin, Yan-Feng, Fu, Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5239489/
https://www.ncbi.nlm.nih.gov/pubmed/27391349
http://dx.doi.org/10.18632/oncotarget.10444
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author Xie, Hong
Xue, Jing-Dong
Chao, Feng
Jin, Yan-Feng
Fu, Qiang
author_facet Xie, Hong
Xue, Jing-Dong
Chao, Feng
Jin, Yan-Feng
Fu, Qiang
author_sort Xie, Hong
collection PubMed
description Although long non-coding RNAs (lncRNAs) are important players in the initiation and progression of many pathological processes, the role of lncRNAs in renal fibrosis still remains unclear. We showed that lncRNA-H19 expression was significantly up-regulated in TGF-β2-induced HK-2 cell fibrosis and unilateral ureteral obstruction (UUO)-induced renal fibrosis in vivo. H19 knockdown significantly attenuated renal fibrosis in vitro and in vivo. LncRNA-H19, miR-17, and fibronectin constituted to a regulatory network involved in renal fibrosis. We also detected up-regulated H19 expression and down-regulated miR-17 expression in the early and advanced animal models of renal fibrosis. This study indicates that H19 up-regulation contributes to renal fibrosis. H19 inhibition might represent a novel anti-fibrotic treatment in renal diseases.
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spelling pubmed-52394892017-01-24 Long non-coding RNA-H19 antagonism protects against renal fibrosis Xie, Hong Xue, Jing-Dong Chao, Feng Jin, Yan-Feng Fu, Qiang Oncotarget Research Paper Although long non-coding RNAs (lncRNAs) are important players in the initiation and progression of many pathological processes, the role of lncRNAs in renal fibrosis still remains unclear. We showed that lncRNA-H19 expression was significantly up-regulated in TGF-β2-induced HK-2 cell fibrosis and unilateral ureteral obstruction (UUO)-induced renal fibrosis in vivo. H19 knockdown significantly attenuated renal fibrosis in vitro and in vivo. LncRNA-H19, miR-17, and fibronectin constituted to a regulatory network involved in renal fibrosis. We also detected up-regulated H19 expression and down-regulated miR-17 expression in the early and advanced animal models of renal fibrosis. This study indicates that H19 up-regulation contributes to renal fibrosis. H19 inhibition might represent a novel anti-fibrotic treatment in renal diseases. Impact Journals LLC 2016-07-06 /pmc/articles/PMC5239489/ /pubmed/27391349 http://dx.doi.org/10.18632/oncotarget.10444 Text en Copyright: © 2016 Xie et al. http://creativecommons.org/licenses/by/2.5/ 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 Research Paper
Xie, Hong
Xue, Jing-Dong
Chao, Feng
Jin, Yan-Feng
Fu, Qiang
Long non-coding RNA-H19 antagonism protects against renal fibrosis
title Long non-coding RNA-H19 antagonism protects against renal fibrosis
title_full Long non-coding RNA-H19 antagonism protects against renal fibrosis
title_fullStr Long non-coding RNA-H19 antagonism protects against renal fibrosis
title_full_unstemmed Long non-coding RNA-H19 antagonism protects against renal fibrosis
title_short Long non-coding RNA-H19 antagonism protects against renal fibrosis
title_sort long non-coding rna-h19 antagonism protects against renal fibrosis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5239489/
https://www.ncbi.nlm.nih.gov/pubmed/27391349
http://dx.doi.org/10.18632/oncotarget.10444
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