Association of the MiR-146aC>G, MiR-149T>C, MiR-196a2T>C, and MiR-499A>G Polymorphisms with Gastric Cancer Risk and Survival in the Korean Population
Overview
Oncology
Authors
Affiliations
We investigated whether four common microRNA polymorphisms (miR-146aC>G [rs2910164], miR-149T>C [rs2292832], miR-196a2T>C [rs11614913], and miR-499A>G [rs3746444]) are associated with the susceptibility and prognosis of gastric cancer in the Korean population. The four microRNA single-nucleotide polymorphisms (SNPs) were identified in a case-control study (461 patients; 447 controls) by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis in the Korean population. When patients were stratified into diffuse and intestinal-type gastric cancer groups, subjects with the miR-499AG and AG + GG genotypes had reduced adjusted odds ratios (AORs) for diffuse-type gastric cancer (AOR = 0.54 with 95% confidence interval [CI] = 0.31-0.97; AOR = 0.57 with 95% CI = 0.33-0.97). In the stratified analyses for gastric cancer risk, the miR-146aGG and CG + GG genotypes were associated with increased risk of gastric cancers among the non-smokers, whereas the miR-149TC and TC + CC genotypes showed lower risk of gastric cancer in males. The miR-196a2CC genotype was associated with elevated gastric cancer risk among females. For gastric cancer prognosis, intestinal-type gastric cancer patients with miR-146aCG + GG genotypes had significantly higher survival rates (log-rank P = 0.030) than patients with the CC genotype, and patients with the miR-499AA genotype had significantly increased survival rates compared to patients with the AG + GG genotypes (log-rank P = 0.013). When miR-146aCG + GG and miR-499AA genotypes were combined, the survival rate of intestinal-type gastric cancer patients was elevated (log-rank P < 0.001). No association was found between gastric or diffuse-type cancer prognosis and other miRNAs. Our data demonstrate that specific miRNA SNPs are associated with gastric cancer susceptibility (miR-499A>G) and prognosis (miR-146aC>G and miR-499A>G) in the Korean population depending on gastric cancer type.
Walter C, Shankaran Z, Kontham S, Ramachandran K, Prakash N, Johnson T Heliyon. 2025; 11(1):e41519.
PMID: 39850417 PMC: 11755044. DOI: 10.1016/j.heliyon.2024.e41519.
Differentially expressed microRNA in prognosis of gastric cancer with Lauren classification.
Chen W, Guo Q, Zhang H, Du Y, Zhou Y, Huang Z Cancer Biomark. 2024; 41(1):41-54.
PMID: 39177588 PMC: 11492042. DOI: 10.3233/CBM-230303.
Wang X, Wang C, Han W, Ma C, Sun J, Wang T Front Oncol. 2024; 14:1374743.
PMID: 38800413 PMC: 11116657. DOI: 10.3389/fonc.2024.1374743.
Effect of rs11614913 Polymorphism on Cancer Susceptibility: Evidence From an Updated Meta-Analysis.
Aziz M, Akter T, Islam M Technol Cancer Res Treat. 2022; 21:15330338221109798.
PMID: 35770306 PMC: 9251994. DOI: 10.1177/15330338221109798.
The Molecular Roles and Clinical Implications of Non-Coding RNAs in Gastric Cancer.
Yue Y, Lin X, Qiu X, Yang L, Wang R Front Cell Dev Biol. 2021; 9:802745.
PMID: 34966746 PMC: 8711095. DOI: 10.3389/fcell.2021.802745.