Your browser doesn't support javascript.
loading
Influence of alkylthio and arylthio derivatives of tert-butylquinone on the induction of DNA damage in a human hepatocellular carcinoma cell line (HepG2).
Djordjevic Aleksic, Jelena; Kolarevic, Stoimir; Jovanovic Maric, Jovana; Kracun-Kolarevic, Margareta; Zegura, Bojana; Stern, Alja; Sladic, Dusan; Novakovic, Irena; Vukovic-Gacic, Branka.
Afiliação
  • Djordjevic Aleksic J; University of Belgrade, Institute for Multidisciplinary Research, Belgrade, Serbia. Electronic address: jelenadjo@imsi.rs.
  • Kolarevic S; University of Belgrade, Institute for Biological Research "Sinisa Stankovic", National Institute of the Republic of Serbia, Belgrade, Serbia.
  • Jovanovic Maric J; University of Belgrade, Institute for Biological Research "Sinisa Stankovic", National Institute of the Republic of Serbia, Belgrade, Serbia.
  • Kracun-Kolarevic M; University of Belgrade, Institute for Biological Research "Sinisa Stankovic", National Institute of the Republic of Serbia, Belgrade, Serbia.
  • Zegura B; Department of Genetic Toxicology and Cancer Biology, National Institute of Biology, Ljubljana, Slovenia.
  • Stern A; Department of Genetic Toxicology and Cancer Biology, National Institute of Biology, Ljubljana, Slovenia.
  • Sladic D; University of Belgrade, Faculty of Chemistry, Belgrade, Serbia.
  • Novakovic I; University of Belgrade, Institute for Chemistry, Technology and Metallurgy, National Institute of the Republic of Serbia, Department for Chemistry, Belgrade, Serbia.
  • Vukovic-Gacic B; University of Belgrade, Centre for Genotoxicology and Ecogenotoxicology, Faculty of Biology, Belgrade, Serbia.
Toxicol In Vitro ; 99: 105882, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38936441
ABSTRACT
The aim of this study was to investigate the effects of tert-butylquinone (TBQ) and its alkylthio and arylthio derivatives on DNA in vitro, using acellular and cellular test systems. Direct interaction with DNA was studied using the plasmid pUC19. Cytotoxic (MTS assay) and genotoxic (comet assay and γH2AX focus assays) effects, and their influence on the cell cycle were studied in the HepG2 cell line. Our results show that TBQ and its derivatives did not directly interact with DNA. The strongest cytotoxic effect on the HepG2 cells was observed for the derivative 2-tert-butyl-5,6-(ethylenedithio)-1,4-benzoquinone (IC50 64.68 and 55.64 µM at 24-h and 48-h treatment, respectively). The tested derivatives did not significantly influence the cell cycle distribution in the exposed cellular populations. However, all derivatives showed a genotoxic activity stronger than that of TBQ in the comet assay, with 2-tert-butyl-5,6-(ethylenedithio)-1,4-benzoquinone producing the strongest effect. The same derivative also induced DNA double-strand breaks in the γH2AX focus assay.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dano ao DNA / Benzoquinonas / Ensaio Cometa Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dano ao DNA / Benzoquinonas / Ensaio Cometa Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article