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Novel Types of Small RNA Exhibit Sequence- and Target-dependent Angiogenesis Suppression Without Activation of Toll-like Receptor 3 in an Age-related Macular Degeneration (AMD) Mouse Model

RNA interference (RNAi) has become a powerful tool for suppressing gene expression in vitro and in vivo. A great deal of evidence has demonstrated the potential for the use of synthetic small interfering RNAs (siRNAs) as therapeutic agents. However, the application of siRNA to clinical medicine is s...

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Autores principales: Takanashi, Masakatsu, Sudo, Katsuko, Ueda, Shinobu, Ohno, Shin-Ichiro, Yamada, Yuko, Osakabe, Yasuhiro, Goto, Hiroshi, Matsunaga, Yoshimichi, Ishikawa, Akio, Usui, Yoshihiko, Kuroda, Masahiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4881762/
https://www.ncbi.nlm.nih.gov/pubmed/26484944
http://dx.doi.org/10.1038/mtna.2015.34
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author Takanashi, Masakatsu
Sudo, Katsuko
Ueda, Shinobu
Ohno, Shin-Ichiro
Yamada, Yuko
Osakabe, Yasuhiro
Goto, Hiroshi
Matsunaga, Yoshimichi
Ishikawa, Akio
Usui, Yoshihiko
Kuroda, Masahiko
author_facet Takanashi, Masakatsu
Sudo, Katsuko
Ueda, Shinobu
Ohno, Shin-Ichiro
Yamada, Yuko
Osakabe, Yasuhiro
Goto, Hiroshi
Matsunaga, Yoshimichi
Ishikawa, Akio
Usui, Yoshihiko
Kuroda, Masahiko
author_sort Takanashi, Masakatsu
collection PubMed
description RNA interference (RNAi) has become a powerful tool for suppressing gene expression in vitro and in vivo. A great deal of evidence has demonstrated the potential for the use of synthetic small interfering RNAs (siRNAs) as therapeutic agents. However, the application of siRNA to clinical medicine is still limited, mainly due to sequence-independent suppression of angiogenesis mediated by Toll-like receptor 3 (TLR3). Here, we describe novel types of synthetic RNA, named nkRNA and PnkRNA, that exhibit sequence-specific gene silencing through RNAi without activating TLRs or RIG-I–like receptor signaling. In addition, we confirmed the therapeutic effect for the novel types of RNA in an animal model of age-related macular degeneration (AMD) without retinal degeneration. These data indicate that nkRNA and PnkRNA are of great potential utility as therapies against blinding choroidal neovascularization due to AMD.
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spelling pubmed-48817622016-06-03 Novel Types of Small RNA Exhibit Sequence- and Target-dependent Angiogenesis Suppression Without Activation of Toll-like Receptor 3 in an Age-related Macular Degeneration (AMD) Mouse Model Takanashi, Masakatsu Sudo, Katsuko Ueda, Shinobu Ohno, Shin-Ichiro Yamada, Yuko Osakabe, Yasuhiro Goto, Hiroshi Matsunaga, Yoshimichi Ishikawa, Akio Usui, Yoshihiko Kuroda, Masahiko Mol Ther Nucleic Acids Original Article RNA interference (RNAi) has become a powerful tool for suppressing gene expression in vitro and in vivo. A great deal of evidence has demonstrated the potential for the use of synthetic small interfering RNAs (siRNAs) as therapeutic agents. However, the application of siRNA to clinical medicine is still limited, mainly due to sequence-independent suppression of angiogenesis mediated by Toll-like receptor 3 (TLR3). Here, we describe novel types of synthetic RNA, named nkRNA and PnkRNA, that exhibit sequence-specific gene silencing through RNAi without activating TLRs or RIG-I–like receptor signaling. In addition, we confirmed the therapeutic effect for the novel types of RNA in an animal model of age-related macular degeneration (AMD) without retinal degeneration. These data indicate that nkRNA and PnkRNA are of great potential utility as therapies against blinding choroidal neovascularization due to AMD. Nature Publishing Group 2015-10 2015-10-20 /pmc/articles/PMC4881762/ /pubmed/26484944 http://dx.doi.org/10.1038/mtna.2015.34 Text en Copyright © 2015 Official journal of the American Society of Gene & Cell Therapy http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Takanashi, Masakatsu
Sudo, Katsuko
Ueda, Shinobu
Ohno, Shin-Ichiro
Yamada, Yuko
Osakabe, Yasuhiro
Goto, Hiroshi
Matsunaga, Yoshimichi
Ishikawa, Akio
Usui, Yoshihiko
Kuroda, Masahiko
Novel Types of Small RNA Exhibit Sequence- and Target-dependent Angiogenesis Suppression Without Activation of Toll-like Receptor 3 in an Age-related Macular Degeneration (AMD) Mouse Model
title Novel Types of Small RNA Exhibit Sequence- and Target-dependent Angiogenesis Suppression Without Activation of Toll-like Receptor 3 in an Age-related Macular Degeneration (AMD) Mouse Model
title_full Novel Types of Small RNA Exhibit Sequence- and Target-dependent Angiogenesis Suppression Without Activation of Toll-like Receptor 3 in an Age-related Macular Degeneration (AMD) Mouse Model
title_fullStr Novel Types of Small RNA Exhibit Sequence- and Target-dependent Angiogenesis Suppression Without Activation of Toll-like Receptor 3 in an Age-related Macular Degeneration (AMD) Mouse Model
title_full_unstemmed Novel Types of Small RNA Exhibit Sequence- and Target-dependent Angiogenesis Suppression Without Activation of Toll-like Receptor 3 in an Age-related Macular Degeneration (AMD) Mouse Model
title_short Novel Types of Small RNA Exhibit Sequence- and Target-dependent Angiogenesis Suppression Without Activation of Toll-like Receptor 3 in an Age-related Macular Degeneration (AMD) Mouse Model
title_sort novel types of small rna exhibit sequence- and target-dependent angiogenesis suppression without activation of toll-like receptor 3 in an age-related macular degeneration (amd) mouse model
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4881762/
https://www.ncbi.nlm.nih.gov/pubmed/26484944
http://dx.doi.org/10.1038/mtna.2015.34
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