Department of Occupational Health and Toxicology, School of Public Health, Fudan University, 138 Yixueyuan Road, Shanghai 200032, China.
Department of Clinical Laboratory, Wenzhou People's Hospital, 57 Canghou Road, Wenzhou 325000, China.
Int J Hyg Environ Health. 2014 Sep;217(7):726-32. doi: 10.1016/j.ijheh.2014.03.003. Epub 2014 Mar 15.
It is well-known that metabolism of benzene is required for the induction of toxicity and consequent health problems. Therefore, genetic variation in benzene (BZ) metabolism genes can influence health outcomes. However, large population studies are needed to provide more evidence for such relationship. We have conducted a large population investigation (385 BZ-exposed shoe workers and 197 matched healthy controls) on the association between inheritance of certain BZ metabolizing genes and the expression of micronuclei (MN). The latter was based on the cytokinesis-blocked MN assay. We analyzed the polymorphisms of GSTM1, GSTT1, GSTP1 (rs1695), CYP2E1 (rs3813867), CYP2E1 (rs2031920), CYP2E1 (rs6413432), mEH exon 3 (rs1051740), mEH exon 4 (rs2234922). Univariate Poisson regression analysis demonstrated that the BZ-exposed workers had significantly increased MN frequency compared with the controls (FR=1.84, 95% CI: 1.56-2.18; P<0.001), and showed a cumulative exposure dose-response relationship. The CYP2E1 rs3813867 mutant allele (CC+GC) (FR 1.15, 95% CI 1.02-1.29; P=0.020) and rs2031920 variant allele (CT+TT) (FR=1.23, 95% CI: 1.09-1.37, P<0.01) was associated with higher MN frequency significantly compared with the wild genotype separately. Furthermore, the MN frequency in rs2031920 variant allele (CT+TT) (FR=1.17, 95% CI: 1.04-1.31, P<0.01) was also higher than the wild genotype when the age, gender and cumulative exposure dose was adjusted in Poisson regression. In addition, the CYP2E1, however, GSTM1null, GSTT1null, GSTP1 rs1695, rs6413432, rs1051740 and rs2234922 polymorphisms showed no association with MN frequency. Our results indicate that two promoter polymorphisms in the CYP2E1 gene, especially the rs2031920 variant allele, were involved with the BZ-induction of MN and may contribute to risk of cancer among exposed workers.
众所周知,苯的代谢是其毒性和随之产生的健康问题的诱导因素。因此,苯(BZ)代谢基因的遗传变异会影响健康结果。然而,需要进行大规模的人群研究来提供更多此类关系的证据。我们进行了一项大型人群调查(385 名 BZ 暴露的鞋厂工人和 197 名匹配的健康对照者),研究了某些 BZ 代谢基因的遗传与微核(MN)表达之间的关系。后者是基于胞质分裂阻断微核试验。我们分析了 GSTM1、GSTT1、GSTP1(rs1695)、CYP2E1(rs3813867)、CYP2E1(rs2031920)、CYP2E1(rs6413432)、mEH 外显子 3(rs1051740)和 mEH 外显子 4(rs2234922)的多态性。单变量泊松回归分析表明,与对照组相比,BZ 暴露工人的 MN 频率显著增加(FR=1.84,95%CI:1.56-2.18;P<0.001),并显示出累积暴露剂量-反应关系。CYP2E1 rs3813867 突变等位基因(CC+GC)(FR 1.15,95%CI 1.02-1.29;P=0.020)和 rs2031920 变异等位基因(CT+TT)(FR=1.23,95%CI:1.09-1.37,P<0.01)与野生基因型相比,MN 频率显著升高。此外,当在泊松回归中调整年龄、性别和累积暴露剂量时,rs2031920 变异等位基因(CT+TT)(FR=1.17,95%CI:1.04-1.31,P<0.01)的 MN 频率也高于野生基因型。此外,CYP2E1 基因的两个启动子多态性,尤其是 rs2031920 变异等位基因,与 BZ 诱导 MN 有关,可能导致暴露工人患癌症的风险增加。