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- W2352172976 abstract "Objective To explore the relationship between genetic polymorphism of CYP2E1,MPO,NQO1,GSTT1,GSTM1 and susceptibility to benzene poisoning(BP).Methods The genotypes of CYP2E1,MPO,NQO1,GSTT1,GSTM1 for 100 patients with benzene poisoning and 90 workers exposed to benzene who were engaged in the same working time and job title as patients with benzene poisoning were detected by PCR-RFLP and multi-PCR.Results There was a 2.82-fold(95% CI:1.42~5.58,P0.05) increased risk of BP in the subjects with NQO1 C609T mutation genotype(T/T) compared with those carrying heterozygous(C/T) and wild type(C/C),and there was a 2.94-fold(95%CI:1.25~6.90,P0.05) increased risk of BP in the subjects with NQO1 C609T mutation genotype(T/T) compared with those carrying wild type(C/C).The subjects with GSTT1 null genotype had a 1.91-fold(95%CI:1.05~3.45,P0.05) increased risk of BP compared with those with GSTT1 non-null genotype.Three genes interaction showed that there was a 20.41-fold(95%CI:3.79~111.11,P0.01) increased risk of BP in subjects with NQO1 C609T mutation genotype(T/T) and GSTT1 null genotype and GSTM1 null genotype compared with those carrying NQO1 C609T heterozygous(C/T) and wild type(C/C) and GSTT1 non-null genotype and GSTM1 non-null genotype.Conclusion The interaction of multi-genes may be an important role to BP.The genetic polymorphisms of 3 genes(NQO1,GSTT1 and GSTM1) leaded to declining of ability of detoxifying in benzene metabolism,so the individual with NQO1 C609T mutation genotype(T/T),GSTT1 null genotype and GSTM1 null genotype is the most susceptive to benzene.It could be suggested as a biomarker to assessment the risk of benzene poisoning for individual." @default.
- W2352172976 created "2016-06-24" @default.
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- W2352172976 date "2007-01-01" @default.
- W2352172976 modified "2023-09-26" @default.
- W2352172976 title "Genetic polymorphisms involved in toxicant-metabolizing enzymes and susceptibility to benzene poisoning" @default.
- W2352172976 hasPublicationYear "2007" @default.
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