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Overexpression of miR-196b and HOXA10 characterize a poor-prognosis gastric cancer subtype

机译:miR-196b和HOXA10的过表达是预后不良的胃癌亚型的特征

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AIM: To identify molecular biologic differences between two gastric adenocarcinoma subgroups presenting different prognoses through the analysis of microRNA and protein expression. METHODS: Array technologies were used to generate 1146 microRNAs and 124 proteins expression profiles of samples from 60 patients with gastric cancer. For the integrative analysis, we used established mRNA expression data published in our previous study. Whole mRNA expression levels were acquired from microarray data for 60 identical gastric cancer patients. Two gastric adenocarcinoma subgroups with distinct mRNA expression profiles presented distinctly different prognoses. MicroRNA and protein expression patterns were compared between gastric cancer tissue and normal gastric tissue and between two different prognostic groups. Aberrantly expressed microRNA, associated mRNA, and protein in patients with poor-prognosis gastric cancer were validated by quantitative reverse transcription polymerase chain reaction and immunochemistry in independent patients. RESULTS: We obtained the expression data of 1146 microRNAs and 124 cancer-related proteins. Four microRNAs were aberrantly expressed in the two prognostic groups and in cancer vs non-cancer tissues (P r = 0.726, P P P P P = 0.017) were clearly over-expressed in the poor-prognosis group. CONCLUSION: Co-activation of miR-196b and HOXA10 characterized a poor-prognosis subgroup of patients with gastric cancer. Elucidation of the biologic function of miR-196b and HOXA10 is warranted.
机译:目的:通过分析微小RNA和蛋白质表达,鉴定两个预后不同的胃腺癌亚组之间的分子生物学差异。方法:采用阵列技术从60例胃癌患者样本中产生1146个microRNA和124个蛋白质表达谱。对于整合分析,我们使用了先前研究中发表的既定的mRNA表达数据。从60名相同胃癌患者的微阵列数据中获得了完整的mRNA表达水平。两个具有不同mRNA表达谱的胃腺癌亚组的预后明显不同。比较了胃癌组织和正常胃组织以及两个不同预后组之间的MicroRNA和蛋白质表达模式。通过定量逆转录聚合酶链反应和免疫化学方法对独立预后不良的胃癌患者中异常表达的microRNA,相关的mRNA和蛋白质进行了验证。结果:我们获得了1146个微RNA和124个癌症相关蛋白的表达数据。在两个预后组中四个microRNA异常表达,在预后较差的组中,癌组织与非癌组织中的过表达显着过高(P r = 0.726,P P P P P = 0.017)。结论:miR-196b和HOXA10的共同激活是胃癌患者预后不良的特征。有必要阐明miR-196b和HOXA10的生物学功能。

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