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Combustion-derived particles from biomass sources differently promote epithelial-to-mesenchymal transition on A549 cells
Combustion-derived particles (CDPs), due to the presence in their composition of several toxic and carcinogenic chemical compounds, such as polycyclic aromatic hydrocarbons (PAHs) and metals, are linked to several respiratory diseases, including lung cancer. Epithelial-to-mesenchymal transition (EMT...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8032642/ https://www.ncbi.nlm.nih.gov/pubmed/33481051 http://dx.doi.org/10.1007/s00204-021-02983-8 |
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author | Marchetti, Sara Bengalli, Rossella Floris, Pamela Colombo, Anita Mantecca, Paride |
author_facet | Marchetti, Sara Bengalli, Rossella Floris, Pamela Colombo, Anita Mantecca, Paride |
author_sort | Marchetti, Sara |
collection | PubMed |
description | Combustion-derived particles (CDPs), due to the presence in their composition of several toxic and carcinogenic chemical compounds, such as polycyclic aromatic hydrocarbons (PAHs) and metals, are linked to several respiratory diseases, including lung cancer. Epithelial-to-mesenchymal transition (EMT) is a crucial step in lung cancer progression, involving several morphological and phenotypical changes. The study aims to investigate how exposure to CDPs from different biomass sources might be involved in cancer development, focusing mainly on the effects linked to EMT and invasion on human A549 lung cells. Biomass combustion-derived particles (BCDPs) were collected from a stove fuelled with pellet, charcoal or wood, respectively. A time course and dose response evaluation on cell viability and pro-inflammatory response was performed to select the optimal conditions for EMT-related studies. A significant release of IL-8 was found after 72 h of exposure to 2.5 μg/cm(2) BCDPs. The EMT activation was then examined by evaluating the expression of some typical markers, such as E-cadherin and N-cadherin, and the possible enhanced migration and invasiveness. Sub-acute exposure revealed that BCDPs differentially modulated cell viability, migration and invasion, as well as the expression of proteins linked to EMT. Results showed a reduction in the epithelial marker E-cadherin and a parallel increase in the mesenchymal markers N-cadherin, mainly after exposure to charcoal and wood. Migration and invasion were also increased. In conclusion, our results suggest that BCDPs with a higher content of organic compounds (e.g. PAHs) in their chemical composition might play a crucial role in inducing pro-carcinogenic effects on epithelial cells. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00204-021-02983-8. |
format | Online Article Text |
id | pubmed-8032642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-80326422021-04-27 Combustion-derived particles from biomass sources differently promote epithelial-to-mesenchymal transition on A549 cells Marchetti, Sara Bengalli, Rossella Floris, Pamela Colombo, Anita Mantecca, Paride Arch Toxicol In Vitro Systems Combustion-derived particles (CDPs), due to the presence in their composition of several toxic and carcinogenic chemical compounds, such as polycyclic aromatic hydrocarbons (PAHs) and metals, are linked to several respiratory diseases, including lung cancer. Epithelial-to-mesenchymal transition (EMT) is a crucial step in lung cancer progression, involving several morphological and phenotypical changes. The study aims to investigate how exposure to CDPs from different biomass sources might be involved in cancer development, focusing mainly on the effects linked to EMT and invasion on human A549 lung cells. Biomass combustion-derived particles (BCDPs) were collected from a stove fuelled with pellet, charcoal or wood, respectively. A time course and dose response evaluation on cell viability and pro-inflammatory response was performed to select the optimal conditions for EMT-related studies. A significant release of IL-8 was found after 72 h of exposure to 2.5 μg/cm(2) BCDPs. The EMT activation was then examined by evaluating the expression of some typical markers, such as E-cadherin and N-cadherin, and the possible enhanced migration and invasiveness. Sub-acute exposure revealed that BCDPs differentially modulated cell viability, migration and invasion, as well as the expression of proteins linked to EMT. Results showed a reduction in the epithelial marker E-cadherin and a parallel increase in the mesenchymal markers N-cadherin, mainly after exposure to charcoal and wood. Migration and invasion were also increased. In conclusion, our results suggest that BCDPs with a higher content of organic compounds (e.g. PAHs) in their chemical composition might play a crucial role in inducing pro-carcinogenic effects on epithelial cells. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00204-021-02983-8. Springer Berlin Heidelberg 2021-01-22 2021 /pmc/articles/PMC8032642/ /pubmed/33481051 http://dx.doi.org/10.1007/s00204-021-02983-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | In Vitro Systems Marchetti, Sara Bengalli, Rossella Floris, Pamela Colombo, Anita Mantecca, Paride Combustion-derived particles from biomass sources differently promote epithelial-to-mesenchymal transition on A549 cells |
title | Combustion-derived particles from biomass sources differently promote epithelial-to-mesenchymal transition on A549 cells
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title_full | Combustion-derived particles from biomass sources differently promote epithelial-to-mesenchymal transition on A549 cells
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title_fullStr | Combustion-derived particles from biomass sources differently promote epithelial-to-mesenchymal transition on A549 cells
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title_full_unstemmed | Combustion-derived particles from biomass sources differently promote epithelial-to-mesenchymal transition on A549 cells
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title_short | Combustion-derived particles from biomass sources differently promote epithelial-to-mesenchymal transition on A549 cells
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title_sort | combustion-derived particles from biomass sources differently promote epithelial-to-mesenchymal transition on a549 cells |
topic | In Vitro Systems |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8032642/ https://www.ncbi.nlm.nih.gov/pubmed/33481051 http://dx.doi.org/10.1007/s00204-021-02983-8 |
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