Abstract | OBJECTIVES: METHODS: The study population was recruited from four MBOCA-producing factories, and included 57 MBOCA-exposed workers and 101 unexposed control workers. Personal characteristics were collected by questionnaire. Plasma 8-OHdG levels were measured by LC/MS/MS. NAT2 alleles were measured by polymerase chain reaction-based restriction fragment length polymorphism (PCR-RFLP). RESULTS: NAT2 polymorphism influenced the plasma 8-OHdG levels of MBOCA-exposed workers, but not of non-exposed workers. No difference between exposed and control groups was found for the crude 8-OHdG levels among rapid, intermediate, and slow acetylators. After adjusting for gender, age, smoking, and alcohol consumption habit, the 8-OHdG concentration in the MBOCA-exposed workers was 0.18pg/ml (95% CI -1.80 to -0.12) lower than the control group among rapid and intermediate acetylators. However, the difference between exposed and control groups was not significant for slow acetylators. CONCLUSION: Gene-environment interactions could play a role in the carcinogenesis of occupational MBOCA exposure. We suggest that the impact of the NAT2 acetylator status is low, if at all, on the generation of the oxidative stress marker 8-OHdG in the investigated exposed group.
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Authors | I-Shen Lin, Pao-Lou Fan, Hong-I Chen, Ching-Hui Loh, Tung-Sheng Shih, Saou-Hsing Liou |
Journal | International journal of hygiene and environmental health
(Int J Hyg Environ Health)
Vol. 216
Issue 4
Pg. 515-20
(Jul 2013)
ISSN: 1618-131X [Electronic] Germany |
PMID | 23491024
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2013 Elsevier GmbH. All rights reserved. |
Chemical References |
- Methylenebis(chloroaniline)
- 8-Hydroxy-2'-Deoxyguanosine
- Arylamine N-Acetyltransferase
- NAT2 protein, human
- Deoxyguanosine
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Topics |
- 8-Hydroxy-2'-Deoxyguanosine
- Acetylation
- Adult
- Arylamine N-Acetyltransferase
(genetics, metabolism)
- Deoxyguanosine
(analogs & derivatives, blood)
- Female
- Gene-Environment Interaction
- Genotype
- Humans
- Male
- Methylenebis(chloroaniline)
(metabolism)
- Occupational Exposure
(analysis)
- Oxidative Stress
- Polymorphism, Genetic
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