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

Arch Toxicol. 2021 Apr;95(4):1379-1390. doi: 10.1007/s00204-021-02983-8. Epub 2021 Jan 22.

Abstract

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/cm2 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.

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

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • A549 Cells
  • Antigens, CD / metabolism
  • Biomass*
  • Cadherins / metabolism
  • Cell Movement / drug effects
  • Cell Survival / drug effects
  • Epithelial-Mesenchymal Transition / drug effects*
  • Humans
  • Lung / cytology
  • Lung / drug effects*
  • Polycyclic Aromatic Hydrocarbons / toxicity*

Substances

  • Antigens, CD
  • CDH1 protein, human
  • CDH2 protein, human
  • Cadherins
  • Polycyclic Aromatic Hydrocarbons