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The effects of 1-nitropyrene on oxidative DNA damage and expression of DNA repair enzymes.

Abstract
Nitropyrenes (NPs) present in diesel and gasoline emissions are mutagenic and carcinogenic in experimental animals. Nitro-reduction of 1-NP causes oxidative stress. It is unclear whether 8-hydroxydeoxyguanosine (8-OH-dG) is produced from 1-NP and whether it contributes to the carcinogenic activity of 1-NP. In this study, we measured the level of reactive oxygen species (ROS) in cultured human lung epithelial cells after exposure to 1-NP and the intracellular level of 8-OH-dG and expression level of the 8-OH-dG repair enzymes. As results, 1-NP induced the generation of 8-OH-dG via ROS, but 8-OH-dG repair enzymes prevented an increase of 8-OH-dG formation in cellular DNA of the A549 cell line below 250 microM of 1-NP. These data suggest that 1-NP can induce oxidative DNA damage by generation of ROS, which may play a role in the carcinogenesis induced by 1-NP. These data also suggest that individuals with impaired DNA repair enzymes might be more susceptible to lung cancer induced by 1-NP.
AuthorsYong-Dae Kim, Young-Jun Ko, Toshihiro Kawamoto, Heon Kim
JournalJournal of occupational health (J Occup Health) Vol. 47 Issue 3 Pg. 261-6 (May 2005) ISSN: 1341-9145 [Print] Australia
PMID15953848 (Publication Type: Journal Article)
Chemical References
  • Mutagens
  • Pyrenes
  • 8-Hydroxy-2'-Deoxyguanosine
  • DNA Repair Enzymes
  • Deoxyguanosine
  • 1-nitropyrene
Topics
  • 8-Hydroxy-2'-Deoxyguanosine
  • Cell Culture Techniques
  • Cell Line
  • DNA Damage (drug effects)
  • DNA Repair Enzymes (metabolism)
  • Deoxyguanosine (analogs & derivatives, biosynthesis)
  • Humans
  • Japan
  • Lung Neoplasms (chemically induced)
  • Mutagens (toxicity)
  • Oxidative Stress (drug effects)
  • Pyrenes (toxicity)

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