Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/1469
Title: Evaluation of genotoxic potential of tert-butylquinone and its derivatives in prokaryotic and eukaryotic test models
Authors: Đorđević, Jelena 
Kolarević, Stoimir 
Jovanović, Jovana
Kostić-Vuković, Jovana
Novaković, Irena
Jeremić, Marko
Sladić, Dušan
Vuković Gačić, Branka 
Keywords: alkylamino and aralkylamino derivatives;Tert-butylquinone;plasmid relaxation;SOS/umuC;genotoxicity;comet assay
Issue Date: 1-Jan-2018
Rank: M22
Journal: Drug and Chemical Toxicology
Abstract: 
© 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group. Tert-butylquinone (TBQ) and its alkylamino and aralkylamino derivatives are of high interest as a potential antitumor agent. Therefore, it was necessary to investigate if the compounds exert undesirable activities such as interaction with DNA molecule which could result in negative side effects in the case of their use in the diseases treatment. The major aim of this study was to investigate genotoxic potential of TBQ and selected derivatives in an acellular model by using plasmid DNA, in the prokaryotic model by the SOS/umuC assay in Salmonella typhimurium TA1535/pSK1002 and in eukaryotic models by using comet assay in human fetal lung cell line (MRC-5) and human liver cancer cell line (HepG2). Results indicated that in the acellular model TBQ and its derivatives do not interact with plasmid pUC19. In the prokaryotic model, only TBQ exerted weak genotoxic potential and only at highly cytotoxic concentrations. In eukaryotic models, genotoxic potential was detected mainly at the highest concentrations of the tested substances but the effect was lower in both cell lines in comparison with benzo[a]pyrene and etoposide which were used as positive controls. Weak genotoxic potential of tested compounds recommends them as good candidates for further testing in development of new antitumor agents.
URI: https://biore.bio.bg.ac.rs/handle/123456789/1469
ISSN: 0148-0545
DOI: 10.1080/01480545.2018.1514043
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