Polymorphisms in RAS/RAF/MEK/ERK Pathway Are Associated with Gastric Cancer

Abstract

The RAS/RAF/MEK/ERK pathway regulates certain cellular functions, including cell proliferation, differentiation, survival, and apoptosis. Dysregulation of this pathway leads to the occurrence and progression of cancers mainly by somatic mutations. This study aimed to assess if polymorphisms of the RAS/RAF/MEK/ERK pathway are associated with gastric cancer. A case-control study of 242 gastric cancer patients and 242 controls was performed to assess the association of 27 single nucleotide polymorphisms (SNPs) in the RAS/RAF/MEK/ERK pathway genes with gastric cancer. Analyses performed under the additive model (allele) showed four significantly associated SNPs: <i>RAF1</i> rs3729931 (Odds ratio (OR) = 1.54, 95%, confidence interval (CI): 1.20⁻1.98, <i>p</i>-value = 7.95 × 10^-4), <i>HRAS</i> rs45604736 (OR = 1.60, 95% CI: 1.16⁻2.22, <i>p</i>-value = 4.68 × 10^-3), <i>MAPK1</i> rs2283792 (OR = 1.45, 95% CI: 1.12⁻1.87, <i>p</i>-value = 4.91 × 10^-3), and <i>MAPK1</i> rs9610417 (OR = 0.60, 95% CI: 0.42⁻0.87, <i>p</i>-value = 6.64 × 10^-3). Functional annotation suggested that those variants or their proxy variants may have a functional effect. In conclusion, this study suggests that <i>RAF1</i> rs3729931, <i>HRAS</i> rs45604736, <i>MAPK1</i> rs2283792, and <i>MAPK1</i> rs9610417 are associated with gastric cancer.