Rogoveanu Ion, Burada Florin, Cucu Mihai Gabriel, Vere Cristin Constantin, Ioana Mihai, Cîmpeanu Raluca Alexandra
Research Center of Gastroenterology and Hepatology, University of Medicine and Pharmacy of Craiova, Craiova, Romania.
Research Center of Gastroenterology and Hepatology; Human Genomics Laboratory, University of Medicine and Pharmacy of Craiova, Craiova, Romania.
J Gastrointestin Liver Dis. 2017 Sep;26(3):231-238. doi: 10.15403/jgld.2014.1121.263.rog.
MicroRNAs (miRNAs) play an important role in the occurrence and progression of human cancers, including gastric cancer. Our hospital-based case-control study aimed to investigate whether four commonly studied single nucleotide polymorphisms (SNPs) have effects on susceptibility to gastric cancer in a Romanian population.
We genotyped the miR-27a rs895819, miR-146a rs2910164, miR-196a2 rs11614913 and miR-499 rs3746444 SNPs by real-time PCR using predesignated TaqMan assays in 430 individuals (142 gastric cancer patients and 288 age and gender matched cancer-free controls). The associations between the investigated miRNA SNPs and gastric cancer risk were assessed by odds ratio (OR) with 95% confidence interval (CI) using logistic regression analysis.
A higher frequency of the miR-27a rs895819 CC genotype (OR 1.98, 95% CI: 1.05-3.73, p=0.036) was found in the patients with gastric cancer compared with the controls. Similar results were observed in a recessive model, the CC genotype was correlated with gastric cancer susceptibility (OR 1.95, 95% CI: 1.07-3.55, p=0.032). In the stratified analysis, the association between miR-27a rs895819 SNP and gastric cancer risk was limited to noncardia (OR 2.08, 95% CI: 1.10-3.94, p=0.027) and intestinal (OR 2.27, 95% CI: 1.05-4.92, p=0.042) subgroups. However, after Bonferroni correction, all associations described above lost statistical significance. No correlation was observed for the remaining SNPs and risk of gastric cancer in any genetic model studied.
This study showed no association of the investigated miRNA SNPs with the risk of gastric cancer in a Romanian population.
微小RNA(miRNA)在包括胃癌在内的人类癌症的发生和发展中起重要作用。我们基于医院的病例对照研究旨在调查4个常用的单核苷酸多态性(SNP)是否对罗马尼亚人群的胃癌易感性有影响。
我们使用预先设计的TaqMan分析通过实时PCR对430名个体(142例胃癌患者和288例年龄和性别匹配的无癌对照)的miR-27a rs895819、miR-146a rs2910164、miR-196a2 rs11614913和miR-499 rs3746444 SNP进行基因分型。使用逻辑回归分析通过比值比(OR)和95%置信区间(CI)评估所研究的miRNA SNP与胃癌风险之间的关联。
与对照组相比,在胃癌患者中发现miR-27a rs895819 CC基因型的频率更高(OR 1.98,95% CI:1.05 - 3.73,p = 0.036)。在隐性模型中观察到类似结果,CC基因型与胃癌易感性相关(OR 1.95,95% CI:1.07 - 3.55,p = 0.032)。在分层分析中,miR-27a rs895819 SNP与胃癌风险之间的关联仅限于非贲门(OR 2.08,95% CI:1.10 - 3.94,p = 0.027)和肠型(OR 2.27,95% CI:1.05 - 4.92,p = 0.042)亚组。然而,经过Bonferroni校正后,上述所有关联均失去统计学意义。在所研究的任何遗传模型中,未观察到其余SNP与胃癌风险之间的相关性。
本研究表明在罗马尼亚人群中,所研究的miRNA SNP与胃癌风险无关联。