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.
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Authors | Yong-Dae Kim, Young-Jun Ko, Toshihiro Kawamoto, Heon Kim |
Journal | Journal of occupational health
(J Occup Health)
Vol. 47
Issue 3
Pg. 261-6
(May 2005)
ISSN: 1341-9145 [Print] Australia |
PMID | 15953848
(Publication Type: Journal Article)
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Chemical References |
- Mutagens
- Pyrenes
- 8-Hydroxy-2'-Deoxyguanosine
- DNA Repair Enzymes
- Deoxyguanosine
- 1-nitropyrene
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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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