DNA Damage Induced by trans, trans-2,4-Decadienal (tt-DDE), a Component of Cooking Oil Fume, in Human Bronchial Epithelial Cells

被引:33
|
作者
Young, Shun-Chieh [1 ]
Chang, Louis W. [1 ]
Lee, Hui-Ling [2 ]
Tsai, Lung-Hung [3 ]
Liu, Yin-Chang [4 ]
Lin, Pinpin [1 ,3 ]
机构
[1] Natl Hlth Res Inst, Div Environm Hlth & Occupat Med, Zhunan, Taiwan
[2] Fu Jen Catholic Univ, Dept Chem, Hsinchuang Taipei, Taiwan
[3] Chung Shan Med Univ, Inst Med & Mol Toxicol, Taichung, Taiwan
[4] Natl Tsing Hua Univ, Inst Mol Med, Hsinchu, Taiwan
关键词
trans, trans-2,4-decadienal; reactive oxygen species; base excision repair; nucleotide excision repair; lung cells; BASE EXCISION-REPAIR; LUNG-CANCER; MUTAGENIC COMPOUNDS; OXIDATIVE STRESS; NONSMOKING WOMEN; COMET ASSAY; GENOTOXICITY; CYTOKINE; SHANGHAI;
D O I
10.1002/em.20550
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Epidemiological studies have demonstrated that cooking oil fumes (COF) are an environmental risk factor for the development of lung adenocarcinoma among nonsmoking females in Taiwan. Aside from polycyclic aromatic hydrocarbons, aldehydes, especially trans, trans-2,4-decadienal (tt-DDE) are found to be abundant in COF. Although there is indication that tt-DDE induces DNA damage, the precise role of tt-DDE in the induction of DNA damage in lung cells is still not clear. When we assessed DNA breaks with the Comet assay, we found that the DNA breaks induced by 1 mu M tt-DDE in human bronchial epithelial cells (BEAS-2B) could be significantly reduced by antioxidants, suggesting that oxidative stress was involved. Indeed, when tt-DDE-treated cells were coincubated with endonuclease III/formamidopyrimidine-DNA glycosylase or with nuclear extract (NE), an enhancement of DNA breaks was observed at 1 hr after tt-DDE exposure. Furthermore, when NE was incubated with an antibody against 8-oxoguanine DNA glycosylase (anti-OGG1), a reduction in tt-DDE/NE-induced DNA breaks could be demonstrated. Since OGG1 is a specific repair enzyme for 8-oxodeoxyguanosine (8-oxo-dG), these findings indicated that 8-oxo-dG was involved. On the other hand, when NE was incubated with antibodies against nucleotide excision repair enzymes, there was a significant reduction in tt-DDE/NE-induced DNA breaks at 4 hr after tt-DDE treatment. These observations indicate that, in addition to early oxidative DNA damage, nonoxidative DNA damage such as bulky adduct formation, was also induced by tt-DDE. Our study further affirms that tt-DDE is genotoxic to human lung cells and can increase carcinogenic risk. Environ. Mol. Mutagen. 51:315-321, 2010. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:315 / 321
页数:7
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