Department of Surgery, Yixing People's Hospital, Yixing, China.
PLoS One. 2013;8(1):e50856. doi: 10.1371/journal.pone.0050856. Epub 2013 Jan 10.
Tumor necrosis factor-α (TNF-α) plays a crucial role in the development and progression of gastric cancer. A functional polymorphism, -308 G>A (rs1800629), which is located in the promoter of TNFA gene, has been suggested to alter the production of TNF-α and influence cancer risk. In the present study, we sought to investigate whether this polymorphism has effects on the risk and progression of gastric cancer in a Chinese population.
We genotyped the TNFA -308 G>A polymorphism using the TaqMan method in a two-stage case-control study comprising a total of 1686 gastric cancer patients and 1895 cancer-free subjects. The logistic regression was used to assess the genetic associations with occurrence and progression of gastric cancer.
We found a significant association between the variant genotypes and increased risk of gastric cancer [P = 0.034, odds ratio (OR) = 1.39, 95% confidence interval (CI) = 1.01-1.67, GA/AA vs. GG]. Similar results were observed in the follow-up replication study. When combined the data from the two studies, we found a more significant association (P = 0.001, OR = 1.34, 95%CI = 1.13-1.59), especially for older subjects (>65 years). Furthermore, the patients carrying the variant genotypes had a significantly greater prevalence of T4 stage of disease (P = 0.001, OR = 2.19, 95%CI = 1.39-3.47) and distant metastasis (P = 0.013, OR = 1.61, 95%CI = 1.10-2.35).
Our results suggest that the functional promoter -308 G>A polymorphism in TNFA influence the susceptibility and progression of gastric cancer in the Chinese population.
肿瘤坏死因子-α(TNF-α)在胃癌的发生和发展中起着至关重要的作用。一个位于 TNFA 基因启动子中的功能多态性-308 G>A(rs1800629),已被提出可改变 TNF-α的产生并影响癌症风险。在本研究中,我们试图探讨该多态性是否会对中国人群胃癌的风险和进展产生影响。
我们采用 TaqMan 法在包括 1686 例胃癌患者和 1895 例无癌对照的两阶段病例对照研究中对 TNFA-308 G>A 多态性进行了基因分型。使用逻辑回归来评估遗传关联与胃癌的发生和进展。
我们发现,与胃癌风险增加相关的变异基因型为 GA/AA(P=0.034,比值比[OR]:1.39,95%置信区间[CI]:1.01-1.67)。在后续的重复研究中也观察到了类似的结果。当合并来自两项研究的数据时,我们发现了更显著的关联(P=0.001,OR:1.34,95%CI:1.13-1.59),特别是对于年龄较大的患者(>65 岁)。此外,携带变异基因型的患者 T4 期疾病(P=0.001,OR:2.19,95%CI:1.39-3.47)和远处转移(P=0.013,OR:1.61,95%CI:1.10-2.35)的发生率明显更高。
我们的结果表明,TNFA 中的功能性启动子-308 G>A 多态性影响了中国人群胃癌的易感性和进展。