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Targeting MicroRNA Function in Respiratory Diseases: Mini-Review

MicroRNAs (miRNAs) are small non-coding RNA molecules that modulate expression of the majority of genes by inhibiting protein translation. Growing literature has identified functional roles for miRNAs across a broad range of biological processes. As such, miRNAs are recognized as potential disease b...

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Autores principales: Maltby, Steven, Plank, Maximilian, Tay, Hock L., Collison, Adam, Foster, Paul S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4740489/
https://www.ncbi.nlm.nih.gov/pubmed/26869937
http://dx.doi.org/10.3389/fphys.2016.00021
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author Maltby, Steven
Plank, Maximilian
Tay, Hock L.
Collison, Adam
Foster, Paul S.
author_facet Maltby, Steven
Plank, Maximilian
Tay, Hock L.
Collison, Adam
Foster, Paul S.
author_sort Maltby, Steven
collection PubMed
description MicroRNAs (miRNAs) are small non-coding RNA molecules that modulate expression of the majority of genes by inhibiting protein translation. Growing literature has identified functional roles for miRNAs across a broad range of biological processes. As such, miRNAs are recognized as potential disease biomarkers and novel targets for therapies. While several miRNA-targeted therapies are currently in clinical trials (e.g., for the treatment of hepatitis C virus infection and cancer), no therapies have targeted miRNAs in respiratory diseases in the clinic. In this mini-review, we review the current knowledge on miRNA expression and function in respiratory diseases, intervention strategies to target miRNA function, and considerations specific to respiratory diseases. Altered miRNA expression profiles have been reported in a number of respiratory diseases, including asthma, chronic obstructive pulmonary disease, cystic fibrosis, and idiopathic pulmonary fibrosis. These include alterations in isolated lung tissue, as well as sputum, bronchoalveolar lavage fluids and peripheral blood or serum. The observed alterations in easily accessible body fluids (e.g., serum) have been proposed as new biomarkers that may inform disease diagnosis and patient management. In a subset of studies, miRNA-targeted interventions also improved disease outcomes, indicating functional roles for altered miRNA expression in disease pathogenesis. In fact, direct administration of miRNA-targeting molecules to the lung has yielded promising results in a number of animal models. The ability to directly administer compounds to the lung holds considerable promise and may limit potential off-target effects and side effects caused by the systemic administration required to treat other diseases.
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spelling pubmed-47404892016-02-11 Targeting MicroRNA Function in Respiratory Diseases: Mini-Review Maltby, Steven Plank, Maximilian Tay, Hock L. Collison, Adam Foster, Paul S. Front Physiol Physiology MicroRNAs (miRNAs) are small non-coding RNA molecules that modulate expression of the majority of genes by inhibiting protein translation. Growing literature has identified functional roles for miRNAs across a broad range of biological processes. As such, miRNAs are recognized as potential disease biomarkers and novel targets for therapies. While several miRNA-targeted therapies are currently in clinical trials (e.g., for the treatment of hepatitis C virus infection and cancer), no therapies have targeted miRNAs in respiratory diseases in the clinic. In this mini-review, we review the current knowledge on miRNA expression and function in respiratory diseases, intervention strategies to target miRNA function, and considerations specific to respiratory diseases. Altered miRNA expression profiles have been reported in a number of respiratory diseases, including asthma, chronic obstructive pulmonary disease, cystic fibrosis, and idiopathic pulmonary fibrosis. These include alterations in isolated lung tissue, as well as sputum, bronchoalveolar lavage fluids and peripheral blood or serum. The observed alterations in easily accessible body fluids (e.g., serum) have been proposed as new biomarkers that may inform disease diagnosis and patient management. In a subset of studies, miRNA-targeted interventions also improved disease outcomes, indicating functional roles for altered miRNA expression in disease pathogenesis. In fact, direct administration of miRNA-targeting molecules to the lung has yielded promising results in a number of animal models. The ability to directly administer compounds to the lung holds considerable promise and may limit potential off-target effects and side effects caused by the systemic administration required to treat other diseases. Frontiers Media S.A. 2016-02-04 /pmc/articles/PMC4740489/ /pubmed/26869937 http://dx.doi.org/10.3389/fphys.2016.00021 Text en Copyright © 2016 Maltby, Plank, Tay, Collison and Foster. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Maltby, Steven
Plank, Maximilian
Tay, Hock L.
Collison, Adam
Foster, Paul S.
Targeting MicroRNA Function in Respiratory Diseases: Mini-Review
title Targeting MicroRNA Function in Respiratory Diseases: Mini-Review
title_full Targeting MicroRNA Function in Respiratory Diseases: Mini-Review
title_fullStr Targeting MicroRNA Function in Respiratory Diseases: Mini-Review
title_full_unstemmed Targeting MicroRNA Function in Respiratory Diseases: Mini-Review
title_short Targeting MicroRNA Function in Respiratory Diseases: Mini-Review
title_sort targeting microrna function in respiratory diseases: mini-review
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4740489/
https://www.ncbi.nlm.nih.gov/pubmed/26869937
http://dx.doi.org/10.3389/fphys.2016.00021
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