AI Article Synopsis

  • The study focuses on butylquinone (TBQ) and its derivatives, examining their potential as antitumor agents and their possible harmful effects, especially regarding DNA interaction.
  • In various models, TBQ and its derivatives were tested for genotoxicity, revealing that TBQ showed minimal genotoxic effects at high concentrations, while the derivatives had even lower effects.
  • These findings suggest that while there are some genotoxic risks, TBQ and its derivatives may still be promising candidates for further research in creating new cancer treatments.

Article Abstract

-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/ assay in 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.

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Source
http://dx.doi.org/10.1080/01480545.2018.1514043DOI Listing

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