Genotoxic effects of camphorquinone and DMT on human oral and intestinal cells

Highlights • Camphorquinone (CQ) induced DNA lesions in OKF6/TERT2 and Caco-2 cells. • This DNA damage is mainly caused by the generation of 8-oxoguanine. • The antioxidant glutathione prevented CQ-associated DNA damage in Caco-2 cells. • Recovery following CQ-treatment significantly reduced DNA dam...

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Veröffentlicht in:Dental materials 2015-10, Vol.31 (10), p.1159-1168
Hauptverfasser: Wessels, Miriam, Rimkus, Julia, Leyhausen, Gabriele, Volk, Joachim, Geurtsen, Werner
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container_end_page 1168
container_issue 10
container_start_page 1159
container_title Dental materials
container_volume 31
creator Wessels, Miriam
Rimkus, Julia
Leyhausen, Gabriele
Volk, Joachim
Geurtsen, Werner
description Highlights • Camphorquinone (CQ) induced DNA lesions in OKF6/TERT2 and Caco-2 cells. • This DNA damage is mainly caused by the generation of 8-oxoguanine. • The antioxidant glutathione prevented CQ-associated DNA damage in Caco-2 cells. • Recovery following CQ-treatment significantly reduced DNA damage in Caco-2 cells.
doi_str_mv 10.1016/j.dental.2015.06.007
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source MEDLINE; Elsevier ScienceDirect Journals
subjects 8-Oxoguanine
Advanced Basic Science
Antioxidants - pharmacology
Bioassay
Caco-2 Cells - drug effects
Camphor - analogs & derivatives
Camphor - toxicity
Camphorquinone
Comet Assay
Damage
Damage detection
Dental materials
Dentistry
Deoxyribonucleic acid
DNA Damage
Genotoxicity
Glutathione - pharmacology
Guanine - analogs & derivatives
Guanine - toxicity
Humans
In Vitro Techniques
Keratinocytes - drug effects
Mouth Mucosa - cytology
Oxidative Stress
Photoinitiators
Reactive oxygen species
Reactive Oxygen Species - toxicity
Recovery
Toluidines - toxicity
title Genotoxic effects of camphorquinone and DMT on human oral and intestinal cells
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