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Common genetic variants at 1q22 and 10q23 and gastric cancer susceptibility in a Korean population

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Tumor Biology

Abstract

Genetic variants at 1q22 and 10q23 were identified as genetic markers of both gastric cancer and esophageal squamous cell carcinoma susceptibility by two genome-wide association studies. The aim of this study was to determine whether rs4072037A > G in MUC1 at 1q22 and rs2274223A > G in PLCE1 at 10q23 are associated with a risk of gastric cancer in a Korean population. We conducted a large-scale case–control study of 3,245 patients with gastric cancer and 1,700 controls. The allele frequencies of rs4072037G and rs2274223G were 11.2 and 25.5 % among patients with gastric cancer, compared with 12.8 and 26.4 %, respectively, among controls. We found that the rs4072037 AG genotype was significantly associated with a reduced risk of gastric cancer [odds ratios (OR) = 0.78; 95 % confidence interval (CI) = 0.67–0.91 for AG vs AA]. Compared with the rs2274223 AA genotype, we found a significant association between the rs2274223 AG genotype and a weakly reduced risk of gastric cancer (OR = 0.87; 95 % CI = 0.76–0.99 for AG vs AA). Our data suggest that genetic variants at 1q22 and 10q23 play a role in gastric carcinogenesis.

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Acknowledgments

This study was supported by grant no. 0720570 from the National R&D Program for Cancer Control, Ministry for Health and Welfare, Republic of Korea.

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Correspondence to Min-Ho Shin.

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Song, HR., Kim, H.N., Kweon, SS. et al. Common genetic variants at 1q22 and 10q23 and gastric cancer susceptibility in a Korean population. Tumor Biol. 35, 3133–3137 (2014). https://doi.org/10.1007/s13277-013-1409-4

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  • DOI: https://doi.org/10.1007/s13277-013-1409-4

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