The Role of Tumor Necrosis Factor-αα| Promoter Polymorphisms in Gastric Carcinoma in Iranians: A Case-Control Study in the North-East of Iran

Mehdi SeilanianToosi, Houshang Rafatpanah, Jalil TavakkolAfshar, MohammadReza GhavamNassiri, HamidReza Sima, Mona MalekzadehMoghani, Rashin Ganjali

Abstract


Background

Host genetic and environmental factors are involved in development of gastric cancer. Tumor necrosis factor (TNF)-α| has a key role in Helicobacter pylori-induced gastritis. We analyzed the association between TNF-α polymorphism and the risk of gastric cancer in an Iranian population residing in northeastern Iran.

Materials and Methods

In a case-control study, the genotyping was carried out by PCR-RFLP in 108 patients with gastric cancer and 100 randomly-selected healthy individuals. The polymorphic sites studied include promoter region of TNF-α at position 308 (G-A transition). H. pylori infection was determined by ELISA assay in 100 patients.

Results

The frequencies of TNF-α 308 GG, AG and AA genotypes were 67%, 29% and 4% for controls and 75.9%, 13.2% and 10.2% for patients. AG genotype significantly reduced the risk of gastric carcinoma (p=0.008). There was no association between TNF-α 308 polymorphisms and the risk of diffuse type gastric carcinoma. Carriers of AG genotype were

associated with a decreased risk of intestinal type gastric carcinoma (OR=0.25, 95% CI: 0.08-0.7). With stratification of patients according to H. pylori infection status, there were no significant differences in the frequencies of genotypes between those with H. pylori-negative gastric carcinoma and controls. However, the frequency of AG genotype was significantly higher among controls than H. pylori-positive cases (OR=0.230, 95% CI: 0.06-0.8). In contrast, AA genotype was significantly more frequent among H. pylori-positive cases compared to the controls (OR=4.1, CI: 1.04-16.4).

Conclusions

Our results suggest an association between TNF-α 308 polymorphism and the risk of gastric cancer in Iranians. The effect is prominent among H. pylori-infected patients and intestinal type of gastric carcinoma.


Keywords


Gastric carcinoma; Cytokine; Polymorphism; Tumor necrosis factor-α; Helicobacter pylori

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