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首页> 外文期刊>DNA and Cell Biology >The Association Between -1304T > G Polymorphism in the Promoter of Mitogen-Activated Protein Kinase Kinase 4 Gene and the Risk of Cervical Cancer in Chinese Population
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The Association Between -1304T > G Polymorphism in the Promoter of Mitogen-Activated Protein Kinase Kinase 4 Gene and the Risk of Cervical Cancer in Chinese Population

机译:丝裂素活化蛋白激酶激酶4基因启动子中-1304T> G多态性与中国人群宫颈癌风险的关系

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Mitogen-activated protein kinase kinase 4 (MKK4) is a critical mediator of stress-activated protein kinase signals that regulate apoptosis, inflammations, and tumorigenesis. Several polymorphisms have been identified in the MKK4 gene. We hypothesized that genetic variants in the MKK4 promoter may alter its functions and thus cancer risk. In the current, hospital-based case-control study of 471 cervical cancer cases and 600 sex and age frequency-matched cancer-free controls in an Eastern Chinese population, we genotyped two common polymorphisms in the MKK4 promoter region (-1304T > G, rs3826392 and -1044A > T, rs3809728)c and assessed their associations with the risk of cervical cancer. We found that compared with the most common -1304TT genotype, carriers of -1304G variant genotypes had a significantly decreased risk of cervical cancer [odds ratio (OR) = 0.71; 95% confidence interval (CI) = 0.53-0.92 for TG, and OR = 0.52; 95% CI = 0.30-0.91 for GG] in an allele dose-response manner (adjusted P-trend = 0.004). Moreover, the luciferase assay showed that the G allele in the promoter significantly increased the transcription activity of the MKK4 gene in vitro and that the MKK4 mRNA expression levels of the G variant carriers was significantly higher in tumor tissues than those of the -1304TT genotype. However, no significant association was observed between the -1044A > T polymorphism and risk of cervical cancer. Our data suggest that the functional -1304G variant in the MKK4 promoter contributes to a decreased risk of cervical cancer by increasing the promoter activity and that the G variant may be a marker for susceptibility to cervical cancer.
机译:丝裂原激活的蛋白激酶激酶4(MKK4)是调节细胞凋亡,炎症和肿瘤发生的应激激活的蛋白激酶信号的关键介体。已在MKK4基因中鉴定出几种多态性。我们假设MKK4启动子中的遗传变异可能会改变其功能,从而改变患癌症的风险。在当前基于医院的病例对照研究中,我们对东方华人人群中的471例宫颈癌病例和600个性别和年龄相匹配的无癌对照进行了基因分型,我们对MKK4启动子区域的两个常见多态性进行了基因分型(-1304T> G, rs3826392和-1044A> T,rs3809728)c并评估了它们与子宫颈癌风险的关系。我们发现,与最常见的-1304TT基因型相比,-1304G变异基因型的携带者患子宫颈癌的风险显着降低[几率(OR)= 0.71; TG的95%置信区间(CI)= 0.53-0.92,OR = 0.52;等位基因剂量反应方式(GG的95%CI = 0.30-0.91)(调整P趋势= 0.004)。此外,荧光素酶测定显示启动子中的G等位基因在体外显着增加了MKK4基因的转录活性,并且在肿瘤组织中G变体载体的MKK4 mRNA表达水平显着高于-1304TT基因型。但是,-1044A> T多态性与子宫颈癌风险之间未发现显着相关性。我们的数据表明,MKK4启动子中的功能性-1304G变异体通过增加启动子活性而有助于降低宫颈癌的风险,并且G变异体可能是宫颈癌易感性的标志物。

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