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细胞色素P450基因多态性与肺癌易感性的相关性分析
引用本文:Gu YF,Zhang ZD,Zhang SC,Zheng SH,Jia HY,Gu SX. 细胞色素P450基因多态性与肺癌易感性的相关性分析[J]. 中华医学杂志, 2007, 87(43): 3064-3068
作者姓名:Gu YF  Zhang ZD  Zhang SC  Zheng SH  Jia HY  Gu SX
作者单位:1. 北京胸科医院肿瘤内科,101149
2. 北京胸科医院内科实验室,101149
3. 北京胸科医院流行病学研究室,101149
基金项目:首都医学发展科研基金资助项目(2002-3069)
摘    要:目的 探讨代谢活化酶细胞色素P4501A1(CYP1A1)、2136(CYP2D6)、2E1(CYP2E1)和代谢解毒酶谷胱甘肽硫转移酶(GSTM1)与肺癌易感性的关系。方法 采用PCR、PCR—RFLP技术检测原发性肺癌组(279例)及对照组(684例)的CYP1A1、CYP2D6、CYP2E1、GSTM1代谢酶基因型,对不同基因型在两组分布频率的差异进行OR值的统计分析。结果 CYP1A1突变等位基因(m)、GSTM1功能缺失型(-)分别可使患肺癌的危险性增加1.64(OR=1.64,95%CI为1.21~2.22,P=0.001)和1.58倍(OR=1.58,95%CI为1,19~2.11,P=0.002)。其中CYP1A1与肺鳞癌,小细胞癌,GSTM1与肺鳞癌及肺腺癌明显相关(均P〈0.05)。同时携带GSTM1(-)和CYP1A1(m)可使患肺癌的危险性明显增加(OR=2.75,95%CI为1.73~4.39,P=0.000)。在重度吸烟人群携带GSTM1(-)、CYP1A1(m)、CYP2D6(W)或CYP2E1A基因型均可使患肺癌的危险性显著增加5.71~11.67倍(P=0.000)。结论携带GSTM1(-)及CYP1A1(m)等位基因型者患肺癌的危险性上升,二者有协同作用。在重度吸烟人群,CYP及GSTM1的检测有利于发现肺癌的高危人群。

关 键 词:肺肿瘤 细胞色素P450 多态性  限制性片段长度
修稿时间:2007-07-31

Combined effects of genetic polymorphisms in cytochrome P450s and GSTM1 on lung cancer susceptibility
Gu Yan-Fei,Zhang Zong-De,Zhang Shu-Cai,Zheng Su-Hua,Jia Hong-Yan,Gu Shu-Xiang. Combined effects of genetic polymorphisms in cytochrome P450s and GSTM1 on lung cancer susceptibility[J]. Zhonghua yi xue za zhi, 2007, 87(43): 3064-3068
Authors:Gu Yan-Fei  Zhang Zong-De  Zhang Shu-Cai  Zheng Su-Hua  Jia Hong-Yan  Gu Shu-Xiang
Affiliation:Department of Oncology, Beijing Chest Hospital, Beijing 101149, China
Abstract:OBJECTIVE: To investigate the relationship between the gene polymorphism of metabolizing enzymes and the genetic susceptibility to lung cancer as well as to study the synergistic effects between smoking and the genes. METHODS: Peripheral blood samples were collected from 279 patients with primary lung cancer and 684 age-, nationality-, and native place-matched controls, including patients with benign diseases and healthy volunteers. PCR-RELP was used to detect the distribution of CYP1A1, 2D6, 2E1, and GSTM1 genotypes. The correlation of these genes with the sensibility to lung cancer was analyzed. RESULTS: The CYP1A1 variant allele frequency of the lung cancer group was 67.4%, significantly higher than that of the control group (55.7%, P = 0.001). GSTM1-null genotype was found to be associated with lung cancer (OR = 1.58, P = 0.002). The risk of lung cancer in the individuals carrying GSTM1-null genotype and CYP1A1 (w/m, m/m) genotype was 2.75 times that of the individuals not carrying these genotypes (P < 0.01). There were no significant differences in the frequencies of CYP2D6 and CYP2E1 genotypes between these two groups. In the heavy smokers GSTM1-null, CYP1A1, CYP2D6, and CYP2E1 genotypes increased the risk of lung cancer by 5.71 - 11.67 times (P = 0.000). CONCLUSION: The individuals who carry GSTM1-null genotype and CYP1A1 (m) genotype have an increase risk of lung cancer. The combined effect of I phase metabolizing enzymes and II phase metabolizing enzymes is observed. In heavy smokers the polymorphism of GSTM1 and CYPs affects the susceptibility to lung cancer.
Keywords:Lung neoplasms   Cytochrome P450   Polymorphism, restriction fragment length
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