Comparative evaluation of the effects of bisphenol derivatives on oxidative stress parameters in HepG2 cells

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Bisphenol A (BPA) BPA is an endocrine-disrupting chemical that has a wide range of uses. Exposure to BPA can be by oral, inhalation, and parenteral routes. Although its use in several products is limited, there is still concern on its adverse health effects, particularly for susceptible populations like children. Alternative bisphenols, such as bisphenol S (BPS) and bisphenol F (BPF), are now being used instead of BPA, although there is little information on the toxicity of these bisphenols. BPF is used as a plasticizer in the production of several industrial materials as well as in the coating of drinks and food cans. BPS is used in curing fast-drying epoxy glues, as a corrosion inhibitor and as a reactant in polymer reactions. In this study, the possible toxic effects of BPA, BPS, and BPF in HepG2 cells were evaluated comparatively. For this purpose, their effects on cytotoxicity, production of intracellular reactive oxygen species (ROS), oxidant/antioxidant parameters, and DNA damage have been examined. The cytotoxicity potentials of different bisphenols were found to be as BPS > BPF > BPA. All bisphenol derivatives caused increases in intracellular ROS production. We observed that all bisphenol derivatives cause an imbalance in some oxidant/antioxidant parameters. Bisphenols also caused significant DNA damage in order of BPF > BPA > BPS. We can suggest that both of the bisphenol derivatives used as alternatives to BPA also showed similar toxicities and may not be considered as safe alternatives. Mechanistic studies are needed to elucidate this issue. © 2022 Informa UK Limited, trading as Taylor & Francis Group.

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AlanDeğerDil
dc.contributor.authorOzyurt, Busra
dc.contributor.authorOzkemahli, Gizem
dc.contributor.authorYirun, Anil
dc.contributor.authorOzyurt, Aylin Balci
dc.contributor.authorBacanli, Merve
dc.contributor.authorBasaran, Nursen
dc.contributor.authorKocer-Gumusel, Belma
dc.contributor.authorErkekoglu, Pinar
dc.date.accessioned2026-10-18T20:27:11.448029782Z
dc.date.available2026-10-18T20:27:11.448029782Z
dc.date.issued2023
dc.description.abstractBisphenol A (BPA) BPA is an endocrine-disrupting chemical that has a wide range of uses. Exposure to BPA can be by oral, inhalation, and parenteral routes. Although its use in several products is limited, there is still concern on its adverse health effects, particularly for susceptible populations like children. Alternative bisphenols, such as bisphenol S (BPS) and bisphenol F (BPF), are now being used instead of BPA, although there is little information on the toxicity of these bisphenols. BPF is used as a plasticizer in the production of several industrial materials as well as in the coating of drinks and food cans. BPS is used in curing fast-drying epoxy glues, as a corrosion inhibitor and as a reactant in polymer reactions. In this study, the possible toxic effects of BPA, BPS, and BPF in HepG2 cells were evaluated comparatively. For this purpose, their effects on cytotoxicity, production of intracellular reactive oxygen species (ROS), oxidant/antioxidant parameters, and DNA damage have been examined. The cytotoxicity potentials of different bisphenols were found to be as BPS > BPF > BPA. All bisphenol derivatives caused increases in intracellular ROS production. We observed that all bisphenol derivatives cause an imbalance in some oxidant/antioxidant parameters. Bisphenols also caused significant DNA damage in order of BPF > BPA > BPS. We can suggest that both of the bisphenol derivatives used as alternatives to BPA also showed similar toxicities and may not be considered as safe alternatives. Mechanistic studies are needed to elucidate this issue. © 2022 Informa UK Limited, trading as Taylor & Francis Group.
dc.description.sponsorshipThis work was supported by the Hacettepe University Research Fund under Grant THD-2020–18518.
dc.identifier.doi10.1080/01480545.2022.2028823
dc.identifier.eissn1525-6014
dc.identifier.endpage322
dc.identifier.issn0148-0545
dc.identifier.issue2
dc.identifier.pmid35045766
dc.identifier.scopus2-s2.0-85123315824
dc.identifier.startpage314
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/12273
dc.identifier.volume46
dc.identifier.wosWOS:000744918700001
dc.language.isoen
dc.publisherTaylor and Francis Ltd.
dc.relation.ispartofDrug and Chemical Toxicology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectBisphenol A
dc.subjectbisphenol F
dc.subjectbisphenol S
dc.subjectcytotoxicity
dc.subjectHepG2 cell line
dc.subjectoxidative stress
dc.subjectAntioxidants
dc.subjectChild
dc.subjectHep G2 Cells
dc.subjectHumans
dc.subjectOxidants
dc.subjectReactive Oxygen Species
dc.subject4,4' isopropylidenediphenol
dc.subjectendocrine disruptor
dc.subjectglutathione
dc.subjectreactive oxygen metabolite
dc.subjectsuperoxide dismutase
dc.subjectantioxidant
dc.subjectbis(4-hydroxyphenyl)sulfone
dc.subjectoxidizing agent
dc.subjectArticle
dc.subjectcell culture
dc.subjectcell viability
dc.subjectcomet assay
dc.subjectcontrolled study
dc.subjectDNA damage
dc.subjectenzyme activity
dc.subjectHep-G2 cell line
dc.subjecthuman
dc.subjecthuman cell
dc.titleComparative evaluation of the effects of bisphenol derivatives on oxidative stress parameters in HepG2 cells
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus23
rdl.citation.wos22
rdl.departmentFaculty of Pharmacy, Department of Pharmaceutical Toxicology, Erzincan Binali Yıldırım University, Erzincan, Turkey.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)