Heated tobacco product emissions induce DNA damage in human bronchial epithelial cells via radical formation
Davigo, Michele Claudino Bastos, Victoria Mengels, Kato Mommers, Alex van Schooten, Frederik-Jan Briedé, Jacco J Jessen, Phyllis Opperhuizen, Antoon Talhout, Reinskje Langie, Sabine AS
Davigo, Michele
Claudino Bastos, Victoria
Mengels, Kato
Mommers, Alex
van Schooten, Frederik-Jan
Briedé, Jacco J
Jessen, Phyllis
Opperhuizen, Antoon
Talhout, Reinskje
Langie, Sabine AS
Series / Report no.
Open Access
Type
Journal Article
Article
Article
Language
en
Date of publication
2025-06-23
Year of publication
Research Projects
Organizational Units
Journal Issue
Title
Heated tobacco product emissions induce DNA damage in human bronchial epithelial cells via radical formation
Translated Title
Published in
Free Radic Res 2025; 59(6-7):463-479
Abstract
IQOS is a heated tobacco product (HTP) claimed to be less harmful than regular cigarettes. It is unknown whether IQOS emissions contain radicals, cause DNA damage or affect the expression of DNA repair markers in human bronchial epithelial cells. This has important implications as IQOS diffusion is quickly growing, but little toxicological and genotoxic information on its emissions is available. Therefore, we determined the presence of radicals in cigarette smoke extract (CSE) and IQOS extract (IQOSE) by Electron Spin Resonance (ESR) spectroscopy and measured their levels of Tobacco-Specific Nitrosamines (TSNAs) with liquid chromatography-mass spectrometry (LC-MS). Next, DNA damage induced by CSE and IQOSE was determined by means of the Fpg-modified comet assay in human bronchial epithelial cells (BEAS-2B). Finally, the mRNA and protein levels of DNA repair markers in response to both extracts were evaluated. CSE contained significantly more reactive oxygen species (ROS) and TSNAs, whereas more carbon/nitrogen-centered radicals were detected in IQOSE. After 1 h exposure, 3%CSE and 5%IQOSE caused DNA oxidation, while 5%IQOSE also induced DNA strand breaks and alkali-labile sites. Exposure of cells to 1% and 3% IQOSE for 4 h upregulated the expression of DNA repair genes, whereas no significant impact on DNA repair protein levels was observed. This study shows that IQOS extract contains significant amounts of radicals and TSNAs, can induce DNA damage and increase the expression of DNA repair genes in human bronchial epithelial cells. Whether IQOS use is associated with higher risk of developing lung cancer remains to be determined.
Regulators should inform society about the DNA damaging properties of IQOS emissions through sensibilization campaigns, key to correctly inform the public about the potential health risks associated with use of IQOS.Regulatory agencies should impose the adoption of clear public health warnings on IQOS packaging and advertisements, emphasizing potential hazardous and genotoxic effects on humans.Industry-free research investigating the genotoxic, mutagenic and tumor-promoting properties of IQOS emissions should be financed and facilitated by governments and health organizations, ensuring that policy decisions are based on unbiased evidence.