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RNA therapeutics – The potential treatment for myocardial infarction

RNA therapeutics mainly control gene expression at the transcript level. In contrast to conventional gene therapy which solely increases production of a protein, delivered RNAs can enhance, reduce or abolish synthesis of a particular protein, which control its relevant activities in a more diverse f...

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Detalles Bibliográficos
Autores principales: Chu, Hunghao, Kohane, Daniel S., Langer, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society for Regenerative Medicine 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6581817/
https://www.ncbi.nlm.nih.gov/pubmed/31245491
http://dx.doi.org/10.1016/j.reth.2016.03.002
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author Chu, Hunghao
Kohane, Daniel S.
Langer, Robert
author_facet Chu, Hunghao
Kohane, Daniel S.
Langer, Robert
author_sort Chu, Hunghao
collection PubMed
description RNA therapeutics mainly control gene expression at the transcript level. In contrast to conventional gene therapy which solely increases production of a protein, delivered RNAs can enhance, reduce or abolish synthesis of a particular protein, which control its relevant activities in a more diverse fashion. Thus, they hold promise to treat many human diseases including myocardial infarction (MI). MI is a serious health burden that causes substantial morbidity and mortality. An unmet clinical need for treating MI is the recovery of cardiac function, which requires regeneration of the functional tissues including the vasculature, nerves, and myocardium. Several classes of RNA therapeutics have been investigated in preclinical MI models, and the results have demonstrated their benefits and encourage their future development. In this review, we summarize the common RNA therapeutic approaches and highlight their application in MI therapy.
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spelling pubmed-65818172019-06-26 RNA therapeutics – The potential treatment for myocardial infarction Chu, Hunghao Kohane, Daniel S. Langer, Robert Regen Ther Review Article RNA therapeutics mainly control gene expression at the transcript level. In contrast to conventional gene therapy which solely increases production of a protein, delivered RNAs can enhance, reduce or abolish synthesis of a particular protein, which control its relevant activities in a more diverse fashion. Thus, they hold promise to treat many human diseases including myocardial infarction (MI). MI is a serious health burden that causes substantial morbidity and mortality. An unmet clinical need for treating MI is the recovery of cardiac function, which requires regeneration of the functional tissues including the vasculature, nerves, and myocardium. Several classes of RNA therapeutics have been investigated in preclinical MI models, and the results have demonstrated their benefits and encourage their future development. In this review, we summarize the common RNA therapeutic approaches and highlight their application in MI therapy. Japanese Society for Regenerative Medicine 2016-06-01 /pmc/articles/PMC6581817/ /pubmed/31245491 http://dx.doi.org/10.1016/j.reth.2016.03.002 Text en © 2016, The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review Article
Chu, Hunghao
Kohane, Daniel S.
Langer, Robert
RNA therapeutics – The potential treatment for myocardial infarction
title RNA therapeutics – The potential treatment for myocardial infarction
title_full RNA therapeutics – The potential treatment for myocardial infarction
title_fullStr RNA therapeutics – The potential treatment for myocardial infarction
title_full_unstemmed RNA therapeutics – The potential treatment for myocardial infarction
title_short RNA therapeutics – The potential treatment for myocardial infarction
title_sort rna therapeutics – the potential treatment for myocardial infarction
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6581817/
https://www.ncbi.nlm.nih.gov/pubmed/31245491
http://dx.doi.org/10.1016/j.reth.2016.03.002
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