Impact of Electronic Cigarettes, Heated Tobacco Products and Conventional Cigarettes on the Generation of Oxidative Stress and Genetic and Epigenetic Lesions in Human Bronchial Epithelial BEAS-2B Cells

Electronic cigarettes (e-cig) and heated tobacco products (HTP) are often used as smoking cessation aids, while the harm reduction effects of these alternatives to cigarettes are still the subject of controversial debate, in particular regarding their carcinogenic potential. The objective of this st...

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Main Authors: Gianni Zarcone, Marie Lenski, Thomas Martinez, Smaïl Talahari, Ophélie Simonin, Guillaume Garçon, Delphine Allorge, Fabrice Nesslany, Jean-Marc Lo-Guidice, Anne Platel, Sébastien Anthérieu
Format: Article
Language:English
Published: MDPI AG 2023-10-01
Series:Toxics
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Online Access:https://www.mdpi.com/2305-6304/11/10/847
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author Gianni Zarcone
Marie Lenski
Thomas Martinez
Smaïl Talahari
Ophélie Simonin
Guillaume Garçon
Delphine Allorge
Fabrice Nesslany
Jean-Marc Lo-Guidice
Anne Platel
Sébastien Anthérieu
author_facet Gianni Zarcone
Marie Lenski
Thomas Martinez
Smaïl Talahari
Ophélie Simonin
Guillaume Garçon
Delphine Allorge
Fabrice Nesslany
Jean-Marc Lo-Guidice
Anne Platel
Sébastien Anthérieu
author_sort Gianni Zarcone
collection DOAJ
description Electronic cigarettes (e-cig) and heated tobacco products (HTP) are often used as smoking cessation aids, while the harm reduction effects of these alternatives to cigarettes are still the subject of controversial debate, in particular regarding their carcinogenic potential. The objective of this study is to compare the effects of e-cig, HTP and conventional cigarette emissions on the generation of oxidative stress and genetic and epigenetic lesions in human bronchial epithelial BEAS-2B cells. Our results show that HTP were less cytotoxic than conventional cigarettes while e-cig were not substantially cytotoxic in BEAS-2B cells. E-cig had no significant effect on the Nrf2 pathway, whereas HTP and cigarettes increased the binding activity of Nrf2 to antioxidant response elements and the expression of its downstream targets HMOX1 and NQO1. Concordantly, only HTP and cigarettes induced oxidative DNA damage and significantly increased DNA strand breaks and chromosomal aberrations. Neither histone modulations nor global DNA methylation changes were found after acute exposure, regardless of the type of emissions. In conclusion, this study reveals that HTP, unlike e-cig, elicit a biological response very similar to that of cigarettes, but only after a more intensive exposure: both tobacco products induce cytotoxicity, Nrf2-dependent oxidative stress and genetic lesions in human epithelial pulmonary cells. Therefore, the health risk of HTP should not be underestimated and animal studies are required in order to determine the tumorigenic potential of these emerging products.
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spelling doaj.art-cf938eea4ee94d84aa680a94a63ce4f72023-11-19T18:21:51ZengMDPI AGToxics2305-63042023-10-01111084710.3390/toxics11100847Impact of Electronic Cigarettes, Heated Tobacco Products and Conventional Cigarettes on the Generation of Oxidative Stress and Genetic and Epigenetic Lesions in Human Bronchial Epithelial BEAS-2B CellsGianni Zarcone0Marie Lenski1Thomas Martinez2Smaïl Talahari3Ophélie Simonin4Guillaume Garçon5Delphine Allorge6Fabrice Nesslany7Jean-Marc Lo-Guidice8Anne Platel9Sébastien Anthérieu10Univ. Lille, CHU Lille, Institut Pasteur de Lille, ULR 4483, IMPECS-IMPact de l’Environnement Chimique sur la Santé, F-59000 Lille, FranceUniv. Lille, CHU Lille, Institut Pasteur de Lille, ULR 4483, IMPECS-IMPact de l’Environnement Chimique sur la Santé, F-59000 Lille, FranceUniv. Lille, CHU Lille, Institut Pasteur de Lille, ULR 4483, IMPECS-IMPact de l’Environnement Chimique sur la Santé, F-59000 Lille, FranceUniv. Lille, CHU Lille, Institut Pasteur de Lille, ULR 4483, IMPECS-IMPact de l’Environnement Chimique sur la Santé, F-59000 Lille, FranceUniv. Lille, CHU Lille, Institut Pasteur de Lille, ULR 4483, IMPECS-IMPact de l’Environnement Chimique sur la Santé, F-59000 Lille, FranceUniv. Lille, CHU Lille, Institut Pasteur de Lille, ULR 4483, IMPECS-IMPact de l’Environnement Chimique sur la Santé, F-59000 Lille, FranceUniv. Lille, CHU Lille, Institut Pasteur de Lille, ULR 4483, IMPECS-IMPact de l’Environnement Chimique sur la Santé, F-59000 Lille, FranceUniv. Lille, CHU Lille, Institut Pasteur de Lille, ULR 4483, IMPECS-IMPact de l’Environnement Chimique sur la Santé, F-59000 Lille, FranceUniv. Lille, CHU Lille, Institut Pasteur de Lille, ULR 4483, IMPECS-IMPact de l’Environnement Chimique sur la Santé, F-59000 Lille, FranceUniv. Lille, CHU Lille, Institut Pasteur de Lille, ULR 4483, IMPECS-IMPact de l’Environnement Chimique sur la Santé, F-59000 Lille, FranceUniv. Lille, CHU Lille, Institut Pasteur de Lille, ULR 4483, IMPECS-IMPact de l’Environnement Chimique sur la Santé, F-59000 Lille, FranceElectronic cigarettes (e-cig) and heated tobacco products (HTP) are often used as smoking cessation aids, while the harm reduction effects of these alternatives to cigarettes are still the subject of controversial debate, in particular regarding their carcinogenic potential. The objective of this study is to compare the effects of e-cig, HTP and conventional cigarette emissions on the generation of oxidative stress and genetic and epigenetic lesions in human bronchial epithelial BEAS-2B cells. Our results show that HTP were less cytotoxic than conventional cigarettes while e-cig were not substantially cytotoxic in BEAS-2B cells. E-cig had no significant effect on the Nrf2 pathway, whereas HTP and cigarettes increased the binding activity of Nrf2 to antioxidant response elements and the expression of its downstream targets HMOX1 and NQO1. Concordantly, only HTP and cigarettes induced oxidative DNA damage and significantly increased DNA strand breaks and chromosomal aberrations. Neither histone modulations nor global DNA methylation changes were found after acute exposure, regardless of the type of emissions. In conclusion, this study reveals that HTP, unlike e-cig, elicit a biological response very similar to that of cigarettes, but only after a more intensive exposure: both tobacco products induce cytotoxicity, Nrf2-dependent oxidative stress and genetic lesions in human epithelial pulmonary cells. Therefore, the health risk of HTP should not be underestimated and animal studies are required in order to determine the tumorigenic potential of these emerging products.https://www.mdpi.com/2305-6304/11/10/847heat-not-burn tobaccoe-cigarettelungcytotoxicitygenotoxicityNrf2
spellingShingle Gianni Zarcone
Marie Lenski
Thomas Martinez
Smaïl Talahari
Ophélie Simonin
Guillaume Garçon
Delphine Allorge
Fabrice Nesslany
Jean-Marc Lo-Guidice
Anne Platel
Sébastien Anthérieu
Impact of Electronic Cigarettes, Heated Tobacco Products and Conventional Cigarettes on the Generation of Oxidative Stress and Genetic and Epigenetic Lesions in Human Bronchial Epithelial BEAS-2B Cells
Toxics
heat-not-burn tobacco
e-cigarette
lung
cytotoxicity
genotoxicity
Nrf2
title Impact of Electronic Cigarettes, Heated Tobacco Products and Conventional Cigarettes on the Generation of Oxidative Stress and Genetic and Epigenetic Lesions in Human Bronchial Epithelial BEAS-2B Cells
title_full Impact of Electronic Cigarettes, Heated Tobacco Products and Conventional Cigarettes on the Generation of Oxidative Stress and Genetic and Epigenetic Lesions in Human Bronchial Epithelial BEAS-2B Cells
title_fullStr Impact of Electronic Cigarettes, Heated Tobacco Products and Conventional Cigarettes on the Generation of Oxidative Stress and Genetic and Epigenetic Lesions in Human Bronchial Epithelial BEAS-2B Cells
title_full_unstemmed Impact of Electronic Cigarettes, Heated Tobacco Products and Conventional Cigarettes on the Generation of Oxidative Stress and Genetic and Epigenetic Lesions in Human Bronchial Epithelial BEAS-2B Cells
title_short Impact of Electronic Cigarettes, Heated Tobacco Products and Conventional Cigarettes on the Generation of Oxidative Stress and Genetic and Epigenetic Lesions in Human Bronchial Epithelial BEAS-2B Cells
title_sort impact of electronic cigarettes heated tobacco products and conventional cigarettes on the generation of oxidative stress and genetic and epigenetic lesions in human bronchial epithelial beas 2b cells
topic heat-not-burn tobacco
e-cigarette
lung
cytotoxicity
genotoxicity
Nrf2
url https://www.mdpi.com/2305-6304/11/10/847
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