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The effect of survivin gene promoter polymorphism on breast cancer

机译:Survivin基因启动子多态性对乳腺癌的影响

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Breast cancer is the most common malignant tumor in women and accounts for about 25% of all cancer diagnoses. Survivin is a member of the apoptosis inhibitor protein family of antiapoptotic proteins. In our study, we investigated one of those, the survivin gene promoter 31G/C polymorphism. Included in this study were 111 breast cancer patients who were operated on in our hospital and 101 healthy female subjects. Blood samples from the healthy subjects and paraffin-embedded tissue samples from the patients were used for DNA extraction and subsequent genetic analysis. PCR-RFLP was used for genotype analysis. We established the clinicopathologic characteristics of patients. No significant difference was found between survivin 31G/C promoter polymorphism of tumor characteristics and breast cancer. Between the control and breast cancer groups, survivin promoter polymorphism 31G/C differences were not significantly different (P = 0.058). The risk of developing cancer, having the relevant GC or CC genotype, is 1.413 times higher than those having genotype GG (95% confidence interval: 1.040 to 1.918). Carrying the C allele was statistically significant in terms of susceptibility to breast cancer. In conclusion, the use of survivin gene polymorphism as a risk factor in breast cancer is recommended based on the results of this study.
机译:乳腺癌是女性中最常见的恶性肿瘤,约占所有癌症诊断的25%。 Survivin是抗凋亡蛋白的凋亡抑制剂蛋白家族的成员。在我们的研究中,我们研究了其中一种,survivin基因启动子31G / C多态性。这项研究包括在我们医院接受手术的111名乳腺癌患者和101名健康女性受试者。来自健康受试者的血液样品和来自患者的石蜡包埋的组织样品被用于DNA提取和随后的遗传分析。 PCR-RFLP用于基因型分析。我们建立了患者的临床病理特征。在肿瘤特征的survivin 31G / C启动子多态性与乳腺癌之间没有发现显着差异。在对照组和乳腺癌组之间,survivin启动子多态性31G / C差异无显着差异(P = 0.058)。具有相关GC或CC基因型的患癌风险比具有GG基因型的患癌风险高1.413倍(95%置信区间:1.040至1.918)。就乳腺癌的敏感性而言,携带C等位基因在统计学上是显着的。总之,根据这项研究的结果,建议使用survivin基因多态性作为乳腺癌的危险因素。

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