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Effects of four single nucleotide polymorphisms in microRNA-coding genes on lung cancer risk.

机译:microRNA编码基因中的四个单核苷酸多态性对肺癌风险的影响。

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摘要

No clear consensus has been reached on the four single nucleotide polymorphisms (miR-196a2 gene rs11614913, miR-146a gene rs2910164, miR-149 gene rs2292832, and miR-499 gene rs3746444) in microRNA-coding genes and lung cancer risk. We performed a meta-analysis in an effort to systematically explore the possible association. A computer retrieval of PubMed, Embase, and Institute for Scientific Information (ISI) Web of Science electronic databases was conducted prior to May 2014. References of retrieved articles were also screened. The fixed effects model and the random effects model were applied for dichotomous outcomes to combine the results of the individual studies. Seven studies including 3,705 cases and 4,099 controls were finally included according to the inclusion criteria. Statistical association could be found between rs11614913 polymorphism and lung cancer [C vs. T: P?=?0.01, odds ratio (OR)?=?1.11, 95?% confidence interval (CI) 1.03-1.20, P heterogeneity?=?0.22, fixed effects model; CC?+?CT vs. TT: P?=?0.01, OR?=?1.18, 95?% CI 1.04-1.34, P heterogeneity?=?0.32, fixed effects model; CC vs. TT: P?=?0.009, OR?=?1.24, 95?% CI 1.06-1.45, P heterogeneity?=?0.34, fixed effects model]. Subgroup analysis found this association in the East Asians. As for rs2910164 polymorphism and lung cancer risk, significant association could be found in allele comparison (G vs. C: P?=?0.03, OR?=?0.92, 95?% CI 0.85-0.99, P heterogeneity?=?0.15, fixed effects model) and in the dominant genetic model (GG?+?CG vs. CC: P?=?0.03, OR?=?0.86, 95?% CI 0.76-0.99, P heterogeneity?=?0.31, fixed effects model). In the East Asian subgroup, association could also be found. No association was observed on rs2292832 or rs3746444 polymorphism and lung cancer. Our study suggested that the miR-196a2 gene rs11614913 polymorphism and the miR-146a gene rs2910164 polymorphism might associate with lung cancer risk.
机译:在microRNA编码基因和肺癌风险方面,尚未就四种单核苷酸多态性(miR-196a2基因rs11614913,miR-146a基因rs2910164,miR-149基因rs2292832和miR-499基因rs3746444)达成明确共识。我们进行了一项荟萃分析,以系统地探索可能的关联。 2014年5月之前,对PubMed,Embase和科学信息研究所(ISI)的Web of Science电子数据库进行了计算机检索。还对检索到的文章的参考文献进行了筛选。将固定效应模型和随机效应模型用于二分结果,以结合各个研究的结果。根据纳入标准,最终纳入了包括3,705例病例和4,099例对照的7项研究。 rs11614913基因多态性与肺癌之间存在统计学联系[C vs. T:P?=?0.01,优势比(OR)?=?1.11,95%置信区间(CI)1.03-1.20,P异质性?=? 0.22,固定效果模型; CC≥CT与TT的关系:P≥0.01,OR≥1.18,95%CI 1.04-1.34,P异质性≥0.32,固定效应模型; CC vs.TT:P≥0.009,OR≥1.24,95%CI 1.06-1.45,P异质性≥0.34,固定效应模型]。亚组分析在东亚人中发现了这种关联。至于rs2910164基因多态性和肺癌风险,在等位基因比较中可以发现显着相关性(G对C:P≥= 0.03,OR≥0.92,95%CI 0.85-0.99,P异质性≥0.15,固定效应模型)和显性遗传模型(GG?+?CG vs.CC:P?=?0.03,OR?=?0.86,95%CI 0.76-0.99,P异质性?=?0.31,固定效应模型)。在东亚亚组中,也可以找到关联。 rs2292832或rs3746444多态性与肺癌之间未发现关联。我们的研究表明,miR-196a2基因rs11614913多态性和miR-146a基因rs2910164多态性可能与肺癌风险相关。

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