华西口腔医学杂志

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饮酒和细胞外超氧化物岐化酶、乙醛脱氢酶2基因多态性与口腔鳞状细胞癌的相关性研究

张超贤1   郭李柯2   史淑敏2   

  1. 1.新乡医学院第一附属医院消化内科;2.口腔科,卫辉 453100
  • 收稿日期:2013-08-15 修回日期:2013-11-20 出版日期:2014-04-01 发布日期:2014-04-01
  • 通讯作者: 张超贤,副主任医师,硕士,E-mail:nn21882001@aliyun.com
  • 作者简介:张超贤,副主任医师,硕士,E-mail:nn21882001@aliyun.com

Correlation between drinking behavior and polymorphisms of extracellular superoxide dismutase, aldehyde dehy-drogenase 2 genes, and oral squamous cell carcinoma

Zhang Chaoxian1, Guo Like2, Shi Shumin2   

  1. 1. Dept. of Gastroen-terology, The First Affiliated Hospital of Xinxiang Medical College, Weihui 453100, China; 2. Dept. of Stomatology, The First Affiliated Hospital of Xinxiang Medical College, Weihui 453100, China
  • Received:2013-08-15 Revised:2013-11-20 Online:2014-04-01 Published:2014-04-01

摘要:

目的   探讨饮酒和细胞外超氧化物岐化酶(EC-SOD)、乙醛脱氢酶2(ALDH2)基因多态性与口腔鳞状细胞癌患病之间的关系。方法   采用病例对照研究的方法,以750例口腔鳞状细胞癌患者(病例组)及750例非癌对照者(对照组)的外周血白细胞为样本,采用聚合酶链反应(PCR)技术分析EC-SOD和ALDH2基因的多态性,并分析该基因多态性与口腔鳞状细胞癌患病的关系。结果   病例组EC-SOD(C/G)和ALDH2变异基因型频率分别为38.27%、69.47%,对照组则为21.07%、44.40%,二者差异有统计学意义(P<0.01)。EC-SOD(C/G)患口腔鳞状细胞癌的风险显著增加(OR=2.32),ALDH2变异基因型的患病风险也显著增加(OR=2.85)。基因突变的协同分析发现,EC-SOD(C/G)/ALDH2变异基因型在病例组和对照组中的分布频率分别为30.67%和6.80%,二者差异有统计学意义(P<0.01)。EC-SOD(C/G)/ALDH2变异基因型患口腔鳞状细胞癌的风险显著增加(OR=8.13)。病例组的饮酒率明显高于对照组(OR=2.70),EC-SOD(C/G)及ALDH2变异基因型与饮酒有协同作用(OR=25.00)。结论   EC-SOD及ALDH2变异基因型和饮酒是口腔鳞状细胞癌的易患因素,三者联合在口腔鳞状细胞癌的发生中有协同作用。

关键词: 口腔鳞状细胞癌, 细胞外超氧化物岐化酶, 乙醛脱氢酶2, 多态现象, 饮酒行为

Abstract:

Objective  To investigate the correlation between drinking behavior and polymorphism combination of extracel-lular superoxide dismutase (EC-SOD) and aldehyde dehydrogenase 2 (ALDH2) genes and oral squamous cell carcinoma. Methods   The genetic polymorphisms of EC-SOD and ALDH2 were analyzed by polymorphism-polymerase chain reaction technique in peripheral blood leukocytes of 750 oral squamous cell carcinoma cases and 750 non-cancer controls. Results   The frequencies of EC-SOD (C/G) and ALDH2 variant genotypes were 38.27% and 69.47% in oral squamous cell carcinoma cases and 21.07% and 44.40% in healthy controls, respectively. Statistical tests showed significant difference in the frequencies between the two groups (P<0.01). The risk of oral squamous cell carcinoma with EC-SOD (C/G) was significantly higher than that of controls (OR=2.32). Individuals carrying ALDH2 variant genotypes had high risk of oral squamous cell carcinoma (OR=2.85). Combined analysis of the polymorphisms showed that percentages of EC-SOD (C/G)/ALDH2 variant genotypes in oral squamous cell carcinoma and control groups were 30.67% and 6.80%, respectively (P<0.01). Individuals carrying EC-SOD (C/G)/ALDH2 variant genotypes had high risk of oral squamous cell carcinoma (OR=8.13). The drinking rate of the case group was significantly higher than that in the control group (OR=2.70). Statistical analysis suggested an interaction between drinking and EC-SOD (C/G) and ALDH2 variant genotypes, which increase risk of oral squamous cell carcinoma (OR=25.00). Conclusion   EC-SOD (C/G) and ALDH2 variant genotypes and drinking are the risk factors in oral squamous cell carcinoma, which could carry out a coordinated attack of oral squamous cell carcinoma.

Key words: oral squamous cell carcinoma, extracellu-lar superoxide dismutase,  aldehyde dehydrogenase 2, polymorphism, drinking