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Dietary folate, one‐carbon metabolism‐related genes, and gastric cancer risk in Korea
Author(s) -
Kim Woori,
Woo Hae Dong,
Lee Jeonghee,
Choi Il Ju,
Kim Young Woo,
Sung Joohon,
Kim Jeongseon
Publication year - 2016
Publication title -
molecular nutrition and food research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.495
H-Index - 131
eISSN - 1613-4133
pISSN - 1613-4125
DOI - 10.1002/mnfr.201500384
Subject(s) - mtrr , methylenetetrahydrofolate reductase , single nucleotide polymorphism , genetics , cancer , genotype , biology , medicine , case control study , population , physiology , gene , endocrinology , oncology , environmental health
Scope We evaluated the interactions between polymorphisms involved in one‐carbon metabolism‐related genes and dietary folate intake in gastric cancer risk within the Korean population through a hospital‐based case‐control study. Methods and results A total of 542 controls and 271 cases were included. Genotype data were selected from data produced by the Affymetrix Axiom ® Exome 319 Array. We considered seven single nucleotide polymorphisms (SNPs) of five genes whose SNPs are located in the coding region with a minor allele frequency > 5%: MTHFR (G1793A, A1298C, C677T), MTR A2756G, MTRR A66G, SHMT1 C1420T, and SLC19A1 G80A. Our study found that MTR A2756G was associated with a decreased gastric cancer risk. MTHFR G1793A showed a statistically significant interaction between dietary folate intake and gastric cancer. Conclusion Our results suggest that MTR A2756G is significantly associated with gastric cancer risk, and that MTHFR G1793A statistically interacts with dietary folate intake. Our findings indicate that gene–folate interactions may contribute to gastric cancer risk.