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AIM:To investigate the association between pre-miR- 146a C/G polymorphism and gastric cancer risk. METHODS:We performed a hospital-based,case-control study using polymerase chain reaction-restriction fragment length polymorphism method in 608 individuals(304 gastric cancer patients and 304 age and sex matched cancer-free controls).RESULTS:The frequencies of pre-miR-146a C/G genotypes in the case group were significantly different from those in the control groups(P=0.037).Compared with CC genotype carriers,subjects with the variant genotypes(GC+GG)had a 58%increased risk of gastric cancer(adjusted OR=1.58,95%CI:1.11-2.20,P= 0.009).Moreover,a higher gastric cancer risk was especially evident in younger individuals aged≤58 years, nonsmokers,and males(adjusted OR=1.76,95%CI: 1.08-2.87,P=0.024;adjusted OR=1.55,95%CI: 1.06-2.28,P=0.025;adjusted OR=1.53,95%CI: 1.04-2.27,P=0.033;respectively). CONCLUSION:Pre-miR-146a C/G polymorphism might be associated with an elevated risk of gastric cancer in Chinese population.
AIM: To investigate the association between pre-miR-146a C / G polymorphism and gastric cancer risk. METHODS: We performed a hospital-based, case-control study using polymerase chain reaction- restriction fragment length polymorphism method in 608 individuals cancer patients and 304 age and sex matched cancer-free controls) .RESULTS: The frequencies of pre-miR-146a C / G genotypes in the case group were significantly different from those in control groups (P = 0.037) .Compared with CC genotype carriers, subjects with the variant genotypes (GC + GG) had a 58% increased risk of gastric cancer (adjusted OR = 1.58, 95% CI: 1.11-2.20, P = 0.009) adjusted in younger individuals aged ≦ 58 years, nonsmokers, and males (adjusted OR = 1.76, 95% CI: 1.08-2.87, P = 0.024; adjusted OR = 1.55, 95% CI: 1.06-2.28, P = 0.025; adjusted OR = 1.53, 95% CI: 1.04-2.27, P = 0.033; respectively). CONCLUSION: Pre-miR-146a C / G polymorphism might be associated with an elevated risk of gastric canceration r in Chinese population.