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首页> 外文期刊>Pathology oncology research: POR >Association of CCND1 Gene c.870G > A Polymorphism with Breast Cancer Risk: A Case-ControlStudy and a Meta-Analysis
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Association of CCND1 Gene c.870G > A Polymorphism with Breast Cancer Risk: A Case-ControlStudy and a Meta-Analysis

机译:CCND1基因C.870G的关联>具有乳腺癌风险的多态性:一种案例 - Controlstudy和Meta分析

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Cyclin D1 (CCND1) plays an essential role in regulating the progress of the cell cycle from G1 to S phase. There is a common c.870G > A polymorphism in the CCND1 gene. The aim of this study was to investigate the association of CCND1 gene c.870G > A polymorphism with breast cancer risk in a case-control study, which followed by a meta-analysis and an in silico analysis. Three hundred and thirty-five subjects composed of 174 women with breast cancer and 161 healthy controls were included in the case-control study. CCND1 gene c.870G > A genotyping was performed by PCR-RFLP. Meta-analysis was done for 14 studies composed of 7281 cases and 6820 controls. Some bioinformatics tools were applied to investigate the effects of c.870G > A on the mRNA splicing and structure. Our data obtained from case-control study revealed that GA genotype (OR: 1.89, 95%CI: 1.12-3.17, p = 0.017), AA genotype (OR: 1.95, 95%CI: 1.08-3.53, p = 0.027), and A allele (OR: 1.44, 95%CI: 1.06-1.95, p = 0.019) were significantly associated with breast cancer risk. The results of meta-analysis showed a significant association between CCND1 c.870G > A polymorphism and breast cancer risk, especially in Caucasian population. In silico analysis revealed that c.870G > A transition affect CCND1 mRNA splicing and secondary structure.
机译:Cyclin D1(CCND1)在调节从G1到S期的细胞周期的进展方面起着重要作用。 CCND1基因中存在常见的C.870g>多态性。本研究的目的是探讨CCND1基因C.870g>在病例对照研究中具有乳腺癌风险的多态性的关键态,其次是在硅分析中的荟萃分析。在案例对照研究中包括三百三十五名由174名患有乳腺癌和161名健康对照组成的受试者组成。 CCND1基因C.870G>通过PCR-RFLP进行基因分型。在7281例和6820个对照组成的14项研究中进行了Meta分析。应用一些生物信息学工具以研究C.870G> A对mRNA拼接和结构的影响。我们从病例对照研究获得的数据显示,GA基因型(或:1.89,95%CI:1.12-3.17,P = 0.017),AA基因型(或:1.95,95%CI:1.08-3.53,P = 0.027),和等位基因(或:1.44,95%CI:1.06-1.95,P = 0.019)与乳腺癌风险显着相关。 Meta分析的结果显示CCND1 C.870G>多态性和乳腺癌风险之间的显着关联,特别是在高加索人群中。在硅分析中,C.870G>过渡影响CCND1 mRNA剪接和二级结构。

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