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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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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 |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-4718015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT oreillysteven micrornasinfibrosisopportunitiesandchallenges |