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MicroRNAs in fibrosis: opportunities and challenges

MicroRNAs (miRNAs) are small, non-coding RNAs that mediate mRNA cleavage, translational repression or mRNA destabilisation and are around 22–25 nucleotides in length via partial complementary binding to the 3′ untranslated region in target transcripts. They are master regulators of gene expression....

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Detalles Bibliográficos
Autor principal: O’Reilly, Steven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4718015/
https://www.ncbi.nlm.nih.gov/pubmed/26762516
http://dx.doi.org/10.1186/s13075-016-0929-x
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author O’Reilly, Steven
author_facet O’Reilly, Steven
author_sort O’Reilly, Steven
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description MicroRNAs (miRNAs) are small, non-coding RNAs that mediate mRNA cleavage, translational repression or mRNA destabilisation and are around 22–25 nucleotides in length via partial complementary binding to the 3′ untranslated region in target transcripts. They are master regulators of gene expression. Fibrosis is an important cause of morbidity and mortality in the world, and there are currently no accepted treatments for fibrosis. Many novel miRNAs are now associated with fibrosis, both organ-specific and systemic, as in the prototypical fibrotic disease systemic sclerosis. Recently, the targets of these altered miRNAs have been validated and defined new biochemical pathways. Dysregulated miRNAs are amenable to therapeutic modulation. This review will examine the role of miRNAs in fibrosis and the opportunities and challenges of targeting them.
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spelling pubmed-47180152016-01-20 MicroRNAs in fibrosis: opportunities and challenges O’Reilly, Steven Arthritis Res Ther Review MicroRNAs (miRNAs) are small, non-coding RNAs that mediate mRNA cleavage, translational repression or mRNA destabilisation and are around 22–25 nucleotides in length via partial complementary binding to the 3′ untranslated region in target transcripts. They are master regulators of gene expression. Fibrosis is an important cause of morbidity and mortality in the world, and there are currently no accepted treatments for fibrosis. Many novel miRNAs are now associated with fibrosis, both organ-specific and systemic, as in the prototypical fibrotic disease systemic sclerosis. Recently, the targets of these altered miRNAs have been validated and defined new biochemical pathways. Dysregulated miRNAs are amenable to therapeutic modulation. This review will examine the role of miRNAs in fibrosis and the opportunities and challenges of targeting them. BioMed Central 2016-01-13 2016 /pmc/articles/PMC4718015/ /pubmed/26762516 http://dx.doi.org/10.1186/s13075-016-0929-x Text en © O’Reilly. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
O’Reilly, Steven
MicroRNAs in fibrosis: opportunities and challenges
title MicroRNAs in fibrosis: opportunities and challenges
title_full MicroRNAs in fibrosis: opportunities and challenges
title_fullStr MicroRNAs in fibrosis: opportunities and challenges
title_full_unstemmed MicroRNAs in fibrosis: opportunities and challenges
title_short MicroRNAs in fibrosis: opportunities and challenges
title_sort micrornas in fibrosis: opportunities and challenges
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4718015/
https://www.ncbi.nlm.nih.gov/pubmed/26762516
http://dx.doi.org/10.1186/s13075-016-0929-x
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