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NQO1和GSTT1基因多态性与慢性苯中毒的危险性 被引量:10

Relation of genetic polymorphism of NQO1 and GSTT1 with risks of chronic benzene poisoning
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摘要 目的 探讨NQO1和GSTT1的基因多态性和苯中毒易感性的关系。方法 采用病例 -对照研究 ,以 15 2名苯中毒工人为病例组 ,15 2名接触苯而没有中毒表现的工人为对照组。采用多聚酶链反应 (PCR)、变性高效液相色谱 (DHPLC)和测序检测NQO1基因的启动子和全部编码区的单核苷酸多态性 (singlenucleotidepolymorphism ,SNP) ,以多重PCR检测GSTT1的基因型。结果 在经常吸烟的人群中 ,携带NQO1c .6 0 9T/T基因型的个体接触苯时发生慢性苯中毒的危险性是C/C和C/T基因型的 7.73倍 (95 %CI:1.71~ 34.97,P =0 .0 10 )。在经常饮酒的人群中 ,携带NQO1第 6外显子T/T突变纯合子的个体在接触苯时发生慢性苯中毒的危险性是C/C和C/T基因型的 11.0 0倍 (95 %CI:1.89~ 6 3.83,P =0 .0 0 5 )。结论 携带NQO1c .6 0 9T/T基因型而又同时吸烟或饮酒的个体对苯中毒可能易感。 Objective To explore the relation between genetic polymorphisms of NQO1,GSTT1 and risks of chronic benzene poisoning(BP). Methods A case-control study was conducted.152 BP patients and 152 workers occupationally exposed to benzene without poisoning manifestations were investigated.Polymerase chain reaction(PCR),denaturing high-performance liquid chromatography(DHPLC) and sequencing were used to detect the single nucleotide polymorphisms(SNPs) of the promoter and complete coding-region of NQO1 gene.Multiple PCR was used to detect GSTT1 genotype. Results In smoking population,there was 7.73-fold(95%CI:1.71~34.97,P=0.010) of risk in BP subjects carrying NQO1c.609 T/T genotype,compared with those carrying C/C and C/T.genotype.In drinking population,the individuals carrying the 6th extron of NQO1c.609 T/T homozygote genotype had a 11.00-fold(95%CI:1.89~63.83,P=0.005) risk of BP compared to those with NQO1c.609 C/T and C/C genotypes. Conclusion The subjects carrying NQO1c.609 T/T genotype and together with the habit of smoking or drinking may be more susceptible to BP.
出处 《中华劳动卫生职业病杂志》 CAS CSCD 北大核心 2002年第5期340-343,T001,共5页 Chinese Journal of Industrial Hygiene and Occupational Diseases
基金 卫生部青年科研基金项目 (96Q0 3 0 ) 教育部回国人员资助项目(1999) 国家自然科学基金项目 (3 0 2 71113 )
关键词 NQO1 GSTT1 危险性 苯中毒 基因多态性 生活方式 Benzene poisoning Genetic polymorphism Life style
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参考文献9

  • 1Smith MT,Zhang LP.Biomarkers of leukemia risk: benzene as a model[].Environmental Health Perspectives.1998
  • 2Puga A,Nebert DW,Mckinnon RA,et al.Genetic polymorphisms in human drug-metabolizing enzymes, potential uses of research genetics to identify genes of toxicological relevance[].Critical Reviews in Toxicology.1997
  • 3Rothman N,Smith MT,Hayes RB,et al.Benzene poisoning, a risk factor for hematological malignancy, is associated with the NQO1 609C→T mutation and rapid fractional excretion of chlorzoxaone[].Cancer Research.1997
  • 4Kuklin A,Munson K,Gjerde M,et al.Detection of single-nucleotide polymorphisms with the WAVETM DNA fragment analysis system[].Genetic Testing.1997
  • 5Schlager JJ,Powis G.Cytosolic NAD(P)H: (quinone-acceptor) oxidoreductase in human normal and tumor tissue: effects of cigarette smoking and alcohol[].International Journal of Cancer.1990
  • 6Dunnen JT,Antonarakis SE.Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion[].Human Mutation.2000
  • 7Traver RD,Horikoshi T,Danenberg KD,et al.NAD(P)H: quinone oxidoreductase gene expression in human colon carcinoma cells: characterization of a mutation which modulates DT-diaphorase activity and mitomycin sensitivity[].Cancer Research.1992
  • 8Ross D,Kepa JK,Winski Sl,et al.NAD(P)H: quinone oxidoereductase 1(NQO1): chemoprotection, bioactivation, gene regulation and genetic polymorphisms[].Chemico Biological Interactions.2000
  • 9Traver RD,Siegel D,Beall HD,et al.Characterization of a polymorphism in NAD(P)H: quinone oxidoreductase (DT-diaphorase)[].British Journal of Cancer.1997

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