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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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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. |
format | Online Article Text |
id | pubmed-5239489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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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