The influence of metabolic gene polymorphisms on urinary 1-hydroxypyrene concentrations in Chinese coke oven workers
Science of The Total Environment, ISSN: 0048-9697, Vol: 381, Issue: 1, Page: 38-46
2007
- 32Citations
- 27Captures
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Metrics Details
- Citations32
- Citation Indexes31
- 31
- CrossRef24
- Policy Citations1
- Policy Citation1
- Captures27
- Readers27
- 27
Article Description
Urinary 1-hydroxypyrene (1-OHP), a biomarker of polycyclic aromatic hydrocarbons (PAHs) exposure, may be influenced by metabolic gene polymorphisms. Such knowledge could benefit us in understanding the inter-individual difference in the mechanism of PAHs-induced carcinogenesis. We investigated the influence of gene polymorphisms on urinary 1-OHP concentrations in 447 coke oven workers from two coking plants in south China. After adjustment for age, plant, level of occupational exposure, body mass index, level of education, alcohol consumption, cigarette smoking and respirator usage, AhR R554K (rs2066853), UGT1A1 −3263T>G (rs4124874) and GSTP1 I105V (rs1695) were associated with urinary 1-OHP excretion with the p -value of 0.053, 0.006 and 0.021, respectively. The concentrations of urinary 1-OHP (Geometric mean, μmol/mol creatinine) in the homozygous major variant carriers and homozygous minor variant carriers for AhR R554K, UGT1A1 −3263T>G and GSTP1 I105V were listed as follows: 4.20 and 5.12, 5.11 and 3.92, 4.93 and 2.91, respectively. GSTT1 present carriers had a significantly higher urinary 1-OHP level than that in null carriers in the case with AhR R554K GA/AA carriers (5.17 vs. 3.64 μmol/mol creatinine, p = 0.038), as well as in the case with UGT1A1 −3263T>G TG/GG carriers (5.67 vs. 3.38 μmol/mol creatinine, p = 0.001). These results showed that AhR, UGT1A1, GSTP1 and GSTT1 polymorphisms were associated with urinary 1-OHP concentrations in Chinese coke oven workers. No influence was found in the association between urinary 1-OHP and other genetic polymorphisms such as CYP1A1, CYP1A2, CYP1B1, CYP2E1, EPHX1, EPHX2 in this population.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0048969707002896; http://dx.doi.org/10.1016/j.scitotenv.2007.02.021; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=34249661122&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/17498780; https://linkinghub.elsevier.com/retrieve/pii/S0048969707002896; https://dx.doi.org/10.1016/j.scitotenv.2007.02.021
Elsevier BV
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