Dialyna Ioanna A, Miyakis Spiros, Georgatou Niki, Spandidos Demetrios A
Department of Virology, Medical School, University of Crete, Heraklion, Crete, Greece.
Oncol Rep. 2003 Nov-Dec;10(6):1829-35.
Genetic polymorphisms of the genes encoding for the xenobiotic metabolizing enzymes result in individual variations in the efficiency of detoxification of environmental carcinogens, and have been extensively associated with variable risk for lung neoplasms in different ethnic and environmental backgrounds. In this study, using PCR-RFLP based assays, we investigated the distribution of genetic polymorphisms in CYP1A1, GSTM1 and GSTT1 genes in Greek lung cancer patients (N=122) and healthy controls (N=178). The frequency of CYP1A1 m1 homozygous genotype was 0.04 in patients and 0.02 in controls (detected in 4.10% of patients and in 1.69% of controls, respectively), that of GSTM1 null genotype was 0.52 in patients and 0.54 in controls, whereas those of GSTT1 null genotype was 0.17 and 0.11, in patients and controls, respectively. The GSTM1 null genotype was more frequent in adenocarcinoma, as well as in lung cancer patients with history of chronic obstructive pulmonary disease (COPD). The GSTT1 null genotype correlated with advanced age of the patients at the time of diagnosis. Three combinations of rare genotypes - in subjects carrying simultaneously deviations from the common genotype in more than one gene - were over-represented in lung cancer patients, compared to control population, and were furthermore significantly associated with history of heavy tobacco consumption in lung cancer patients. The results imply involvement of specific genotype combinations of CYP1A1, GSTM1 and GSTT1 alleles in the development of lung cancer in heavy smokers.
编码外源性代谢酶的基因的遗传多态性导致个体对环境致癌物的解毒效率存在差异,并在不同种族和环境背景下与肺癌的可变风险广泛相关。在本研究中,我们使用基于PCR-RFLP的检测方法,调查了希腊肺癌患者(N = 122)和健康对照者(N = 178)中CYP1A1、GSTM1和GSTT1基因的遗传多态性分布。CYP1A1 m1纯合基因型在患者中的频率为0.04,在对照者中为0.02(分别在4.10%的患者和1.69%的对照者中检测到),GSTM1缺失基因型在患者中的频率为0.52,在对照者中为0.54,而GSTT1缺失基因型在患者和对照者中的频率分别为0.17和0.11。GSTM1缺失基因型在腺癌以及有慢性阻塞性肺疾病(COPD)病史的肺癌患者中更为常见。GSTT1缺失基因型与患者诊断时的高龄相关。与对照人群相比,肺癌患者中同时携带多个基因常见基因型偏差的三种罕见基因型组合的比例过高,并且与肺癌患者的大量吸烟史显著相关。结果表明,CYP1A1、GSTM1和GSTT1等位基因的特定基因型组合参与了重度吸烟者肺癌的发生。