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首页> 外文期刊>DNA and Cell Biology >Association of Long Noncoding RNAs Polymorphisms with the Risk of Esophagogastric Junction Adenocarcinoma: A Three-Center Study of 1063 Cases and 1677 Controls
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Association of Long Noncoding RNAs Polymorphisms with the Risk of Esophagogastric Junction Adenocarcinoma: A Three-Center Study of 1063 Cases and 1677 Controls

机译:长度非划分RNA多态性与食管胃部结腺癌风险的关联:三中心研究1063例和1677例

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Increasing evidence suggested that long noncoding RNAs (lncRNAs) variants may be involved in the progression of various cancers. However, the association of the lncRNAs polymorphisms with the risk for esophagogastric junction adenocarcinoma (EGJA) is still unknown. In this case-control study, we selected two cancer-related lncRNAs polymorphisms (rs944289 C > T and rs7990916 C>T), and recruited a total of 1063 EGJA patients and 1677 noncancer controls to determine whether the lncRNAs rs944289 C > T and rs7990916 C > T polymorphisms could influence EGJA susceptibility and lymph node status. And SNPscan (TM) genotyping assay was applied to test the genotypes of the mentioned two variants. We found no statistically significant differences in the distribution of lncRNAs rs944289 C > T and rs7990916 C > T polymorphisms between EGJA patients and healthy controls. Similar negative findings were also revealed in the correlation of those polymorphisms with different lymph node status. However, after adjustment by multiple environmental factors, including gender, age, drinking, and smoking consumption, the stratified analyses showed that the lncRNAs rs944289 C > T variant was significantly related with the risk of EGJA in <60 years populations [CT vs. CC: adjusted odds ratio (OR) = 0.75, 95% confidence interval (CI) = 0.58-0.98, p = 0.032] and ever smoking populations (CT/CC vs. TT: adjusted OR = 1.65, 95% CI = 1.11-2.46, p = 0.013). In short, this population-based study highlights that lncRNAs rs944289 C > T polymorphism may be associated with genetic susceptibility to EGJA in the <60 years and ever smoking populations.
机译:越来越多的证据表明,长度非编码RNA(LNCRNA)变体可以参与各种癌症的进展。然而,LNCRNA多态性与食管胃部结腺癌(EGJA)的风险的关联仍然未知。在这种情况下,我们选择了两种癌症相关的LNCRNA多态性(RS944289 C> T和RS7990916 C> T),并招募了总共1063名EGJA患者和1677名非癌症控制,以确定LNCRNA RS944289 C> T和RS7990916 C> T多态性可以影响EGJA易感性和淋巴结状态。和SnPSCAN(TM)基因分型测定用于测试所述两种变体的基因型。我们发现在EGJA患者和健康对照之间的LNCRNAS RS944289 C> T和RS7990916 C> T多态性中没有发现统计学上显着差异。在具有不同淋巴结状态的多态性的相关性中也揭示了类似的阴性结果。然而,在调整多种环境因素后,包括性别,年龄,饮酒和吸烟消耗,分层分析表明,LNCRNASR944289C> T变体与<60岁人群的egja的风险显着相关[CT与CC :调整后的差距(或)= 0.75,95%置信区间(CI)= 0.58-0.98,P = 0.032]和evs吸烟群体(CT / CC对TT:调整或= 1.65,95%CI = 1.11-2.46 ,p = 0.013)。简而言之,基于人口的研究突出显示,LNCRNASR944289 C> T多态性可能与egja的遗传易感性相关联于<60年和曾经吸烟的人群。

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