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Signaling Pathways Regulated by Silica Nanoparticles

Silica nanoparticles are a class of molecules commonly used in drug or gene delivery systems that either facilitate the delivery of therapeutics to specific drug targets or enable the efficient delivery of constructed gene products into biological systems. Some in vivo or in vitro studies have demon...

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Detalles Bibliográficos
Autores principales: Hsu, Shih-Yi, Morris, Robert, Cheng, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7961477/
https://www.ncbi.nlm.nih.gov/pubmed/33807638
http://dx.doi.org/10.3390/molecules26051398
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author Hsu, Shih-Yi
Morris, Robert
Cheng, Feng
author_facet Hsu, Shih-Yi
Morris, Robert
Cheng, Feng
author_sort Hsu, Shih-Yi
collection PubMed
description Silica nanoparticles are a class of molecules commonly used in drug or gene delivery systems that either facilitate the delivery of therapeutics to specific drug targets or enable the efficient delivery of constructed gene products into biological systems. Some in vivo or in vitro studies have demonstrated the toxic effects of silica nanoparticles. Despite the availability of risk management tools in response to the growing use of synthetic silica in commercial products, the molecular mechanism of toxicity induced by silica nanoparticles is not well characterized. The purpose of this study was to elucidate the effects of silica nanoparticle exposure in three types of cells including human aortic endothelial cells, mouse-derived macrophages, and A549 non-small cell lung cancer cells using toxicogenomic analysis. The results indicated that among all three cell types, the TNF and MAPK signaling pathways were the common pathways upregulated by silica nanoparticles. These findings may provide insight into the effects of silica nanoparticle exposure in the human body and the possible mechanism of toxicity.
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spelling pubmed-79614772021-03-17 Signaling Pathways Regulated by Silica Nanoparticles Hsu, Shih-Yi Morris, Robert Cheng, Feng Molecules Article Silica nanoparticles are a class of molecules commonly used in drug or gene delivery systems that either facilitate the delivery of therapeutics to specific drug targets or enable the efficient delivery of constructed gene products into biological systems. Some in vivo or in vitro studies have demonstrated the toxic effects of silica nanoparticles. Despite the availability of risk management tools in response to the growing use of synthetic silica in commercial products, the molecular mechanism of toxicity induced by silica nanoparticles is not well characterized. The purpose of this study was to elucidate the effects of silica nanoparticle exposure in three types of cells including human aortic endothelial cells, mouse-derived macrophages, and A549 non-small cell lung cancer cells using toxicogenomic analysis. The results indicated that among all three cell types, the TNF and MAPK signaling pathways were the common pathways upregulated by silica nanoparticles. These findings may provide insight into the effects of silica nanoparticle exposure in the human body and the possible mechanism of toxicity. MDPI 2021-03-05 /pmc/articles/PMC7961477/ /pubmed/33807638 http://dx.doi.org/10.3390/molecules26051398 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hsu, Shih-Yi
Morris, Robert
Cheng, Feng
Signaling Pathways Regulated by Silica Nanoparticles
title Signaling Pathways Regulated by Silica Nanoparticles
title_full Signaling Pathways Regulated by Silica Nanoparticles
title_fullStr Signaling Pathways Regulated by Silica Nanoparticles
title_full_unstemmed Signaling Pathways Regulated by Silica Nanoparticles
title_short Signaling Pathways Regulated by Silica Nanoparticles
title_sort signaling pathways regulated by silica nanoparticles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7961477/
https://www.ncbi.nlm.nih.gov/pubmed/33807638
http://dx.doi.org/10.3390/molecules26051398
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