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首页> 外文期刊>Genetic testing and molecular biomarkers >miRNA-Related Polymorphisms in miR-423 (rs6505162) and PEX6 (rs1129186) and Risk of Esophageal Squamous Cell Carcinoma in an Iranian Cohort
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miRNA-Related Polymorphisms in miR-423 (rs6505162) and PEX6 (rs1129186) and Risk of Esophageal Squamous Cell Carcinoma in an Iranian Cohort

机译:miRNA-Related多态性在mir - 423 (rs6505162)和PEX6 (rs1129186)和食管的风险鳞状细胞癌在伊朗的队列

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Aims: Iran is located in the Asian esophageal cancer belt. It is a high-risk region for esophageal squamous cell carcinoma (ESCC). The extent to which genetic components, especially variants within miRNAs or their binding sites, contribute to risk of ESCC in the region is not yet fully understood. Herein, tests were done on an Iranian cohort to evaluate the association of miRNA-related polymorphisms in miR-423 (rs6505162) and peroxisomal biogenesis factor 6 (PEX6) (rs1129186 within a miR-149-5p-binding site) with the risk of ESCC risk. Methods: This study recruited 200 ESCC patients and 300 healthy individuals. Genotyping was performed using the polymerase chain reaction-restriction fragment length polymorphism method. Target genes and biological processes that are regulated by miR-423 and may be affected by a change in miR-423 expression were identified by in silico analysis. Results: Logistic regression analyses revealed an association between rs6505162 and ESCC, assuming codominant (AA vs. CC, odds ratios, OR [95% confidence interval, CI]: 0.32 [0.15-0.69], p-value: 0.0076), recessive (AA vs. CC+CA, OR [95% CI]: 0.35 [0.16-0.73], p-value: 0.0027), and log-additive models (OR [95% CI]: 0.69 [0.52-0.91], p-value: 0.0084). No significant association was observed for PEX6 rs1129186. In silico analyses revealed several genes and biological processes that are regulated by miR-423 in ESCC. Conclusion: This study identified the first evidence of an association of a miRNA-related variant with risk of ESCC in an Iranian cohort. PEX6 rs1129186 may not modulate the risk of ESCC in the cohort.
机译:目的:伊朗位于亚洲的食管癌症的腰带。食管鳞状细胞癌(ESCC)。程度的遗传成分,特别是在microrna或其结合位点变异,导致风险地区ESCC的不是然而完全理解。伊朗人评估协会miRNA-related多态性mir - 4236 (rs6505162)和过氧化物酶病生物起源因素内(PEX6) (rs1129186 mir - 149 - 5 - p -绑定网站)ESCC风险的风险。研究招募了200名ESCC患者和300名健康个人。聚合酶链reaction-restriction片段长度多态性的方法。生物过程的监管mir - 423,可能是受变化的影响mir - 423表达被在网上确认分析。显示一个rs6505162和之间的联系ESCC,假设共显性的(AA与CC,几率比率,或(95%置信区间):0.32(0.15 - -0.69),假定值:0.0076),隐性(AA vs。CC + CA,或(95%置信区间):0.35(0.16 - -0.73),假定值:0.0027),和log-additive模型(或(95%置信区间):0.69(0.52 - -0.91),假定值:0.0084)。重要的协会是PEX6观察rs1129186。基因和生物过程监管ESCC mir - 423。确定一个协会的第一个证据miRNA-related变体ESCC的风险一个伊朗的队列。调节ESCC的队列的风险。

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