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Intranasal administration of resveratrol successfully prevents lung cancer in A/J mice
Lung cancer is the most lethal cancer in the world. About 80% of lung cancer deaths are linked to tobacco use. As a complement to tobacco control, efficient chemoprevention strategies are needed to tackle lung cancer epidemic. Resveratrol is one of the most studied natural products, notably for its...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155121/ https://www.ncbi.nlm.nih.gov/pubmed/30250304 http://dx.doi.org/10.1038/s41598-018-32423-0 |
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author | Monteillier, Aymeric Voisin, Aymone Furrer, Pascal Allémann, Eric Cuendet, Muriel |
author_facet | Monteillier, Aymeric Voisin, Aymone Furrer, Pascal Allémann, Eric Cuendet, Muriel |
author_sort | Monteillier, Aymeric |
collection | PubMed |
description | Lung cancer is the most lethal cancer in the world. About 80% of lung cancer deaths are linked to tobacco use. As a complement to tobacco control, efficient chemoprevention strategies are needed to tackle lung cancer epidemic. Resveratrol is one of the most studied natural products, notably for its cancer chemoprevention properties. However, its low oral bioavailability has often limited the translation of in vitro activities to in vivo effects. While oral administration of resveratrol effectively inhibited colorectal carcinogenesis, it failed to protect mice from chemically-induced lung carcinogenesis. Therefore, non-invasive parenteral routes must be considered to bring resveratrol to the lungs. In the present study, intranasal administration of a concentrated formulation proved to be a valid method to expose the lungs to a sufficient amount of resveratrol. This formulation was administered three times a week for 25 weeks to A/J mice having 4-[methyl(nitroso)amino]-1-(3-pyridinyl)-1-butanone-induced lung carcinogenesis. Resveratrol-treated mice showed a 27% decrease in tumour multiplicity, with smaller tumours, resulting in 45% decrease in tumour volume/mouse. In vitro investigations highlighted apoptosis as a potential mechanism of action. This study presents an effective way to overcome resveratrol low oral bioavailability, encouraging a reevaluation of its use in future clinical trials. |
format | Online Article Text |
id | pubmed-6155121 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61551212018-09-28 Intranasal administration of resveratrol successfully prevents lung cancer in A/J mice Monteillier, Aymeric Voisin, Aymone Furrer, Pascal Allémann, Eric Cuendet, Muriel Sci Rep Article Lung cancer is the most lethal cancer in the world. About 80% of lung cancer deaths are linked to tobacco use. As a complement to tobacco control, efficient chemoprevention strategies are needed to tackle lung cancer epidemic. Resveratrol is one of the most studied natural products, notably for its cancer chemoprevention properties. However, its low oral bioavailability has often limited the translation of in vitro activities to in vivo effects. While oral administration of resveratrol effectively inhibited colorectal carcinogenesis, it failed to protect mice from chemically-induced lung carcinogenesis. Therefore, non-invasive parenteral routes must be considered to bring resveratrol to the lungs. In the present study, intranasal administration of a concentrated formulation proved to be a valid method to expose the lungs to a sufficient amount of resveratrol. This formulation was administered three times a week for 25 weeks to A/J mice having 4-[methyl(nitroso)amino]-1-(3-pyridinyl)-1-butanone-induced lung carcinogenesis. Resveratrol-treated mice showed a 27% decrease in tumour multiplicity, with smaller tumours, resulting in 45% decrease in tumour volume/mouse. In vitro investigations highlighted apoptosis as a potential mechanism of action. This study presents an effective way to overcome resveratrol low oral bioavailability, encouraging a reevaluation of its use in future clinical trials. Nature Publishing Group UK 2018-09-24 /pmc/articles/PMC6155121/ /pubmed/30250304 http://dx.doi.org/10.1038/s41598-018-32423-0 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Monteillier, Aymeric Voisin, Aymone Furrer, Pascal Allémann, Eric Cuendet, Muriel Intranasal administration of resveratrol successfully prevents lung cancer in A/J mice |
title | Intranasal administration of resveratrol successfully prevents lung cancer in A/J mice |
title_full | Intranasal administration of resveratrol successfully prevents lung cancer in A/J mice |
title_fullStr | Intranasal administration of resveratrol successfully prevents lung cancer in A/J mice |
title_full_unstemmed | Intranasal administration of resveratrol successfully prevents lung cancer in A/J mice |
title_short | Intranasal administration of resveratrol successfully prevents lung cancer in A/J mice |
title_sort | intranasal administration of resveratrol successfully prevents lung cancer in a/j mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155121/ https://www.ncbi.nlm.nih.gov/pubmed/30250304 http://dx.doi.org/10.1038/s41598-018-32423-0 |
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