4.7 Article

Combustion-derived particles from biomass sources differently promote epithelial-to-mesenchymal transition on A549 cells

Journal

ARCHIVES OF TOXICOLOGY
Volume 95, Issue 4, Pages 1379-1390

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00204-021-02983-8

Keywords

Biomass combustion-derived particles; Epithelial-to-mesenchymal transition; Interleukin-8; Lung cancer

Categories

Funding

  1. Universita degli Studi di Milano - Bicocca
  2. Italian Ministry of Foreign Affairs and International Cooperation [PGR00786]

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Exposure to combustion-derived particles from biomass sources can potentially induce pro-carcinogenic effects on epithelial cells, with a focus on EMT and invasion processes. This study found that biomass combustion particles differentially modulated cell viability, migration, invasion, and markers linked to EMT. A higher content of organic compounds in the particles may play a crucial role in these effects.
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 mu g/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.

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