The -308G/A Polymorphism of the Tumor Necrosis Factor-alpha Gene Is Associated with the Risk of Upper Aerodigestive Tract Cancer: A Meta-analysis

被引:9
|
作者
Wang, Jiayi [1 ]
Jin, Xin [1 ]
Wang, Hui [2 ]
Yang, Jiantang [3 ]
Wang, Lili [1 ]
Lei, Lei [1 ]
Li, Xiaoxu [1 ]
Zhou, Yu [1 ]
Zeng, Xin [1 ]
Jiang, Lu [1 ]
Liao, Ga [1 ]
Dan, Hongxia [1 ]
Chen, Qianming [1 ]
机构
[1] Sichuan Univ, West China Hosp Stomatol, State Key Lab Oral Dis, Chengdu 610064, Sichuan, Peoples R China
[2] Capital Med Univ, Sch Stomatol, Dept Oral Med, Beijing, Peoples R China
[3] Zunyi Med Coll, Stomatol Hosp, Zunyi, Guizhou, Peoples R China
来源
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
epidemiology; gene polymorphism; meta-analysis; tumor necrosis factor-alpha; upper aerodigestive tract cancer; SQUAMOUS-CELL CARCINOMA; PROMOTER POLYMORPHISM; TNF-ALPHA; SUSCEPTIBILITY; INFLAMMATION; POPULATION; ALCOHOL; SMOKING; REGION;
D O I
10.1620/tjem.229.245
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Tumor necrosis factor-alpha (TNF-alpha) has been proposed to contribute to the development of upper aerodigestive tract (UADT) cancer that is characterized by poor prognosis. The G-to-A nucleotide change at -308 of the TNF-alpha gene (-308G/A polymorphism) can increase the expression level of TNF-alpha and thus may affect the genetic susceptibility of UADT cancer. The association between the -308G/A polymorphism and UADT cancer has been widely studied, but the results published are quite controversial. To obtain a more precise conclusion, we performed a meta-analysis including 1,751 patients and 3,345 controls. The results indicated that the AA genotype of the -308G/A polymorphism had a 54%-increased risk of UADT cancer, compared with the G carriers (CC and GA genotypes) [odds ratio (OR) = 1.54, 95% confidence interval (Cl): 1.07-2.21]. After stratified by ethnicity, the AA genotype was associated with increased risk of UADT cancers in South Asians (OR = 33.18 and 95% Cl: 1.92-573.62 for AA vs. GA+GG) but not in Caucasians or East Asians. After stratified by tumor site, the -308G/A polymorphism was associated with increased risks of oropharynx cancer (OR = 2.68 and 95% Cl: 1.34-5.35 for AA vs. GA+GG) but not associated with esophagus or larynx cancer. After stratified by histological type, the -308G/A polymorphism was associated with increased risks of squamous cell carcinoma (OR = 1.81 and 95% Cl: 1.15-2.84 for AA vs. GA+GG) but not associated with adenocarcinoma. Our results indicate that the -308G/A polymorphism might contribute to an increased risk of UADT cancer susceptibility.
引用
收藏
页码:245 / 254
页数:10
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