Limited mutagenicity of electronic cigarettes in mouse or human cells in vitro

•E-cig are increasingly popular among adult chronic smokers and adolescent never smokers.•The carcinogenic potential of e-cig use in humans is unknown.•E-cig from select brands have limited mutagenicity in mouse/human cells in vitro. Electronic cigarettes (e-cig), which are promoted as safe alternat...

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Veröffentlicht in:Lung cancer (Amsterdam, Netherlands) Netherlands), 2017-10, Vol.112, p.41-46
Hauptverfasser: Tommasi, Stella, Bates, Steven E., Behar, Rachel Z., Talbot, Prue, Besaratinia, Ahmad
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container_end_page 46
container_issue
container_start_page 41
container_title Lung cancer (Amsterdam, Netherlands)
container_volume 112
creator Tommasi, Stella
Bates, Steven E.
Behar, Rachel Z.
Talbot, Prue
Besaratinia, Ahmad
description •E-cig are increasingly popular among adult chronic smokers and adolescent never smokers.•The carcinogenic potential of e-cig use in humans is unknown.•E-cig from select brands have limited mutagenicity in mouse/human cells in vitro. Electronic cigarettes (e-cig), which are promoted as safe alternatives to tobacco cigarettes or as aides to smoking cessation, are becoming increasingly popular among adult chronic smokers and adolescents experimenting with tobacco products. Despite the known presence of toxicants and carcinogens in e-cig liquid and vapor, the possible carcinogenic effects of e-cig use in humans are unknown. We have utilized two validated in vitro model systems to investigate whether e-cig vapor induces mutation in mouse or human cells. We have exposed transgenic mouse fibroblasts in vitro to e-cig vapor extracts prepared from three popular brands, and determined the induction of mutagenesis in a reporter gene, the cII transgene. Furthermore, we have treated the pSP189 plasmid with e-cig vapor extract, transfected human fibroblast cells with the e-cig-treated plasmid, and screened for the induced mutations in the supF gene. We observed no statistically significant increases in relative mutant frequency in the cII transgene or supF gene in the e-cig treated mouse or human cells, respectively. Our data indicate that e-cig vapor extracts from the selected brands and at concentrations tested in this study have limited mutagenicity in both mouse and human cells in vitro.
doi_str_mv 10.1016/j.lungcan.2017.07.035
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source ScienceDirect Journals (5 years ago - present)
subjects cII transgene
Mouse embryonic fibroblasts
Mutation
supF assay
Vaping
title Limited mutagenicity of electronic cigarettes in mouse or human cells in vitro
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