Novel form of miR-29b suppresses bleomycin-induced pulmonary fibrosis.

MicroRNA 29b (miR-29b) replacement therapy is effective for suppressing fibrosis in a mouse model. However, to develop clinical applications for miRNA mimics, the side effects of nucleic acid drugs have to be addressed. In this study, we focused on miRNA mimics in order to develop therapies for idio...

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Main Authors: Yuko Yamada, Masakatsu Takanashi, Katsuko Sudo, Shinobu Ueda, Shin-Ichiro Ohno, Masahiko Kuroda
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5325218?pdf=render
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spelling doaj-2590509697614e49a7c25dd9ae3a40dc2020-11-25T01:58:44ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01122e017195710.1371/journal.pone.0171957Novel form of miR-29b suppresses bleomycin-induced pulmonary fibrosis.Yuko YamadaMasakatsu TakanashiKatsuko SudoShinobu UedaShin-Ichiro OhnoMasahiko KurodaMicroRNA 29b (miR-29b) replacement therapy is effective for suppressing fibrosis in a mouse model. However, to develop clinical applications for miRNA mimics, the side effects of nucleic acid drugs have to be addressed. In this study, we focused on miRNA mimics in order to develop therapies for idiopathic pulmonary fibrosis. We developed a single-stranded RNA, termed "miR-29b Psh-match," that has a unique structure to avoid problems associated with the therapeutic uses of miRNAs. A comparison of miR-29b Psh-match and double-stranded one, termed "miR-29b mimic" indicated that the single-stranded form was significantly effective towards fibrosis according to both in vivo and in vitro experiments. This novel form of miR-29b may become the foundation for developing an effective therapeutic drug for pulmonary fibrosis.http://europepmc.org/articles/PMC5325218?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Yuko Yamada
Masakatsu Takanashi
Katsuko Sudo
Shinobu Ueda
Shin-Ichiro Ohno
Masahiko Kuroda
spellingShingle Yuko Yamada
Masakatsu Takanashi
Katsuko Sudo
Shinobu Ueda
Shin-Ichiro Ohno
Masahiko Kuroda
Novel form of miR-29b suppresses bleomycin-induced pulmonary fibrosis.
PLoS ONE
author_facet Yuko Yamada
Masakatsu Takanashi
Katsuko Sudo
Shinobu Ueda
Shin-Ichiro Ohno
Masahiko Kuroda
author_sort Yuko Yamada
title Novel form of miR-29b suppresses bleomycin-induced pulmonary fibrosis.
title_short Novel form of miR-29b suppresses bleomycin-induced pulmonary fibrosis.
title_full Novel form of miR-29b suppresses bleomycin-induced pulmonary fibrosis.
title_fullStr Novel form of miR-29b suppresses bleomycin-induced pulmonary fibrosis.
title_full_unstemmed Novel form of miR-29b suppresses bleomycin-induced pulmonary fibrosis.
title_sort novel form of mir-29b suppresses bleomycin-induced pulmonary fibrosis.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description MicroRNA 29b (miR-29b) replacement therapy is effective for suppressing fibrosis in a mouse model. However, to develop clinical applications for miRNA mimics, the side effects of nucleic acid drugs have to be addressed. In this study, we focused on miRNA mimics in order to develop therapies for idiopathic pulmonary fibrosis. We developed a single-stranded RNA, termed "miR-29b Psh-match," that has a unique structure to avoid problems associated with the therapeutic uses of miRNAs. A comparison of miR-29b Psh-match and double-stranded one, termed "miR-29b mimic" indicated that the single-stranded form was significantly effective towards fibrosis according to both in vivo and in vitro experiments. This novel form of miR-29b may become the foundation for developing an effective therapeutic drug for pulmonary fibrosis.
url http://europepmc.org/articles/PMC5325218?pdf=render
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AT masakatsutakanashi novelformofmir29bsuppressesbleomycininducedpulmonaryfibrosis
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AT shinobuueda novelformofmir29bsuppressesbleomycininducedpulmonaryfibrosis
AT shinichiroohno novelformofmir29bsuppressesbleomycininducedpulmonaryfibrosis
AT masahikokuroda novelformofmir29bsuppressesbleomycininducedpulmonaryfibrosis
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