Benzene poisoning, a risk factor for hematological malignancy, is associated with the NQO1 609C-T mutation and rapid fractional excretion of chlorzoxazone.
Benzene is a ubiquitous occupational hematotoxin and leukemogen, but people vary in their response to this toxic agent.
To evaluate the impact of interindividual variation in enzymes that activate (ie., CYP2E1) and detoxify (i.e., NQO1) benzene and its metabolites, we carried out a case-control study in Shanghai, China, of occupational benzene poisoning (BP ; i. e, hematotoxicity), which we show is itself strongly associated with subsequent development of acute nonlymphocytic leukemia and the related myelodysplastic syndromes (relative risk, 70.6 ; 95% confidence interval, 11.4-439.3).
CYP2E1 and NQO1 genotypes were determined by PCR-RFLP, and CYP2E1 enzymatic activity was estimated by the fractional excretion of chlorzoxazone (fe6-OH) for 50 cases of BP and 50 controls.
Subjects with both a rapid fe6-OH) and two copies of the NQO1 609C-T mutation had a 7.6-fold (95% confidence interval, 1.8-31.2) increased risk of BP compared to subjects with a slow fe6-OH who carried one or two wild-type NQOI alleles.
In contrast, the CYP2EI PstI/RsaI polymorphism did not influence BP risk.
This is the first report that provides evidence of human susceptibility to benzene-related disease.
Further evaluation of susceptibility for hematotoxicity and hematological malignancy among workers with a history of occupational exposure to benzene is warranted.
Mots-clés Pascal : Benzène, Métabolite, Facteur risque, Chlorzoxazone, Toxicité, Sang, Exposition professionnelle, Homme, Etude cohorte, Leucémie non lymphocytaire, Myélodysplasique syndrome, Intoxication, Génotype, Cytochrome P450, Mutation, Isozyme, Enzyme, Activité enzymatique, Carcinogène, Solvant organique, Composé aromatique, Hémopathie maligne, Chine, Asie, Gène CYP2E1
Mots-clés Pascal anglais : Benzene, Metabolite, Risk factor, Chlorzoxazone, Toxicity, Blood, Occupational exposure, Human, Cohort study, Nonlymphocytic leukemia, Myelodysplastic syndrome, Poisoning, Genotype, Cytochrome P450, Mutation, Isozyme, Enzyme, Enzymatic activity, Carcinogen, Organic solvent, Aromatic compound, Malignant hemopathy, China, Asia
Notice produite par :
Inist-CNRS - Institut de l'Information Scientifique et Technique
Cote : 97-0424587
Code Inist : 002B04E02. Création : 19/12/1997.