Uematsu F, Ikawa S, Kikuchi H, Sagami I, Kanamaru R, Abe T, Satoh K, Motomiya M, Watanabe M
Department of Molecular Genetics, Tohoku University, Sendai, Japan.
Pharmacogenetics. 1994 Apr;4(2):58-63. doi: 10.1097/00008571-199404000-00002.
Polymorphic metabolism of certain chemical carcinogens may result in differences in susceptibility to cancers. Human CYP2E1 (cytochrome P450IIE1) is an enzyme involved in the metabolic activation of precarcinogens such as nitrosamines. We detected a restriction fragment length polymorphism (RFLP) of the human CYP2E1 gene for the restriction endonuclease Dra I. The distribution of this polymorphism was examined among lung cancer patients (n = 91), patients with cancer of the digestive tract (n = 45) and controls (n = 76). A significant difference in the distribution was observed between lung cancer patients and controls (chi 2 = 11.4 with 2 df; p < 0.005). On the other hand, there was no significant difference between patients between cancer of the digestive tract and controls (chi 2 = 4.87 with 2 df; NS). This finding suggests that the Dra I polymorphism of the CYP2E1 gene is associated with susceptibility to lung cancer. In addition, an association was found between the amount of lifelong smoking exposure and the distribution of the genotypes of the RFLP among lung cancer patients. The distribution pattern seemed deviated from that of controls especially in the population of low smoking exposure. Our Northern blot analysis data using RNA from human liver autopsy samples suggest that the Dra I polymorphism might be associated with the gene expression of CYP2E1 at mRNA level.
某些化学致癌物的多态性代谢可能导致癌症易感性的差异。人类细胞色素P450IIE1(CYP2E1)是一种参与亚硝胺等前致癌物代谢活化的酶。我们检测了人类CYP2E1基因针对限制性内切酶Dra I的限制性片段长度多态性(RFLP)。在肺癌患者(n = 91)、消化道癌症患者(n = 45)和对照组(n = 76)中检查了这种多态性的分布。在肺癌患者和对照组之间观察到分布有显著差异(χ2 = 11.4,自由度为2;p < 0.005)。另一方面,消化道癌症患者与对照组之间没有显著差异(χ2 = 4.87,自由度为2;无统计学意义)。这一发现表明,CYP2E1基因的Dra I多态性与肺癌易感性相关。此外,在肺癌患者中发现终生吸烟暴露量与RFLP基因型分布之间存在关联。这种分布模式似乎偏离了对照组,尤其是在低吸烟暴露人群中。我们使用人类肝脏尸检样本的RNA进行的Northern印迹分析数据表明,Dra I多态性可能在mRNA水平与CYP2E1的基因表达相关。