Kortunay S, Koseler A, Orhan Kara C, Topuz B, Omer Atalay E
Department of Pharmacology, Faculty of Medicine, Pamukkale University, Denizli, Turkey.
Methods Find Exp Clin Pharmacol. 2010 Apr;32(3):187-91. doi: 10.1358/mf.2010.32.3.1440739.
Squamous cell carcinoma of the head and neck (SCCHN) have been reported to be related to both genetic and environmental factors, including alcohol consumption and alcohol-metabolizing enzymes such as alcohol dehydrogenase (ADH). We conducted a hospital-based, case-control study including 50 cases with diagnosed SCCHN and 100 controls with non-neoplastic conditions such as upper respiratory tract infection. The genomic DNA was isolated from peripheral blood leukocytes. The ADH1C1 wild-type and ADH1C2 variant alleles were analyzed with an RFLP method by using SspI as restriction enzyme. The ADH1C1 allele frequencies were 0.89 (CI95% = 0.84-0.91) in controls and 0.77 (CI95% = 0.71-0.83) in cases, and respective frequencies of the ADH1C2 allele were 0.11 (CI95% = 0.07-0.14) and 0.23 (CI95% = 0.17-0.29) among controls and cases (P = 0.01). The ADH1C*1/1 genotype frequency was significantly higher in the control group (77%) compared to that of the cases (58%) (P = 0.02).These findings suggest that a lower presence of ADH1C1 allele is associated with SCCHN, but larger numbers are needed to more precisely estimate the interaction, if any, with ADH1C. Interestingly, the ADH1C allele and genotype frequencies in our control group living in Denizli were significantly different compared to a previously published report from healthy volunteers living in Ankara (P < 0.0001).
据报道,头颈部鳞状细胞癌(SCCHN)与遗传和环境因素均有关,包括饮酒以及酒精代谢酶如乙醇脱氢酶(ADH)。我们开展了一项基于医院的病例对照研究,纳入50例确诊为SCCHN的患者以及100例患有非肿瘤性疾病(如上呼吸道感染)的对照。从外周血白细胞中分离基因组DNA。以SspI作为限制性内切酶,采用RFLP方法分析ADH1C1野生型和ADH1C2变异等位基因。对照组中ADH1C1等位基因频率为0.89(95%CI = 0.84 - 0.91),病例组中为0.77(95%CI = 0.71 - 0.83),对照组和病例组中ADH1C2等位基因的相应频率分别为0.11(95%CI = 0.07 - 0.14)和0.23(95%CI = 0.17 - 0.29)(P = 0.01)。对照组中ADH1C*1/1基因型频率(77%)显著高于病例组(58%)(P = 0.02)。这些发现表明,ADH1C1等位基因的低表达与SCCHN相关,但需要更多数量的样本才能更精确地评估与ADH1C的相互作用(如果存在的话)。有趣的是,与之前发表的来自安卡拉健康志愿者的报告相比,我们居住在代尼兹利的对照组中的ADH1C等位基因和基因型频率存在显著差异(P < 0.0001)。