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Non-viral siRNA delivery to the lung()

SiRNAs exert their biological effect by guiding the degradation of their cognate mRNA sequence, thereby shutting down the corresponding protein production (gene silencing by RNA interference or RNAi). Due to this property, siRNAs are emerging as promising therapeutic agents for the treatment of inhe...

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Detalles Bibliográficos
Autores principales: Thomas, Mini, Lu, James J., Chen, Jianzhu, Klibanov, Alexander M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7103292/
https://www.ncbi.nlm.nih.gov/pubmed/17459519
http://dx.doi.org/10.1016/j.addr.2007.03.003
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author Thomas, Mini
Lu, James J.
Chen, Jianzhu
Klibanov, Alexander M.
author_facet Thomas, Mini
Lu, James J.
Chen, Jianzhu
Klibanov, Alexander M.
author_sort Thomas, Mini
collection PubMed
description SiRNAs exert their biological effect by guiding the degradation of their cognate mRNA sequence, thereby shutting down the corresponding protein production (gene silencing by RNA interference or RNAi). Due to this property, siRNAs are emerging as promising therapeutic agents for the treatment of inherited and acquired diseases, as well as research tools for the elucidation of gene function in both health and disease. Because of their lethality and prevalence, lung diseases have attracted particular attention as targets of siRNA-mediated cures. In addition, lung is accessible to therapeutic agents via multiple routes, e.g., through the nose and the mouth, thus obviating the need for targeting and making it an appealing target for RNAi-based therapeutic strategies. The clinical success of siRNA-mediated interventions critically depends upon the safety and efficacy of the delivery methods and agents. Delivery of siRNAs relevant to lung diseases has been attempted through multiple routes and using various carriers in animal models. This review focuses on the recent progress in non-viral delivery of siRNAs for the treatment of lung diseases, particularly infectious diseases. The rapid progress will put siRNA-based therapeutics on fast track to the clinic.
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spelling pubmed-71032922020-03-31 Non-viral siRNA delivery to the lung() Thomas, Mini Lu, James J. Chen, Jianzhu Klibanov, Alexander M. Adv Drug Deliv Rev Article SiRNAs exert their biological effect by guiding the degradation of their cognate mRNA sequence, thereby shutting down the corresponding protein production (gene silencing by RNA interference or RNAi). Due to this property, siRNAs are emerging as promising therapeutic agents for the treatment of inherited and acquired diseases, as well as research tools for the elucidation of gene function in both health and disease. Because of their lethality and prevalence, lung diseases have attracted particular attention as targets of siRNA-mediated cures. In addition, lung is accessible to therapeutic agents via multiple routes, e.g., through the nose and the mouth, thus obviating the need for targeting and making it an appealing target for RNAi-based therapeutic strategies. The clinical success of siRNA-mediated interventions critically depends upon the safety and efficacy of the delivery methods and agents. Delivery of siRNAs relevant to lung diseases has been attempted through multiple routes and using various carriers in animal models. This review focuses on the recent progress in non-viral delivery of siRNAs for the treatment of lung diseases, particularly infectious diseases. The rapid progress will put siRNA-based therapeutics on fast track to the clinic. Elsevier B.V. 2007-03-30 2007-03-15 /pmc/articles/PMC7103292/ /pubmed/17459519 http://dx.doi.org/10.1016/j.addr.2007.03.003 Text en Copyright © 2007 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Thomas, Mini
Lu, James J.
Chen, Jianzhu
Klibanov, Alexander M.
Non-viral siRNA delivery to the lung()
title Non-viral siRNA delivery to the lung()
title_full Non-viral siRNA delivery to the lung()
title_fullStr Non-viral siRNA delivery to the lung()
title_full_unstemmed Non-viral siRNA delivery to the lung()
title_short Non-viral siRNA delivery to the lung()
title_sort non-viral sirna delivery to the lung()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7103292/
https://www.ncbi.nlm.nih.gov/pubmed/17459519
http://dx.doi.org/10.1016/j.addr.2007.03.003
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