Department of Biotechnology, Institute of Molecular and Cell Biology, University of Tartu, Riia 23, 51010 Tartu, Estonia.
Int J Cancer. 2013 Jun 15;132(12):2884-93. doi: 10.1002/ijc.27981. Epub 2012 Dec 27.
The prognostic and diagnostic value of microRNA (miRNA) expression aberrations in lung cancer has been studied intensely in recent years. However, due to the application of different technological platforms and small sample size, the miRNA expression profiling efforts have led to inconsistent results between the studies. We performed a comprehensive meta-analysis of 20 published miRNA expression studies in lung cancer, including a total of 598 tumor and 528 non-cancerous control samples. Using a recently published robust rank aggregation method, we identified a statistically significant miRNA meta-signature of seven upregulated (miR-21, miR-210, miR-182, miR-31, miR-200b, miR-205 and miR-183) and eight downregulated (miR-126-3p, miR-30a, miR-30d, miR-486-5p, miR-451a, miR-126-5p, miR-143 and miR-145) miRNAs. We conducted a gene set enrichment analysis to identify pathways that are most strongly affected by altered expression of these miRNAs. We found that meta-signature miRNAs cooperatively target functionally related and biologically relevant genes in signaling and developmental pathways. We have shown that such meta-analysis approach is suitable and effective solution for identification of statistically significant miRNA meta-signature by combining several miRNA expression studies. This method allows the analysis of data produced by different technological platforms that cannot be otherwise directly compared or in the case when raw data are unavailable.
近年来,人们对 microRNA(miRNA)表达异常在肺癌中的预后和诊断价值进行了深入研究。然而,由于应用了不同的技术平台和样本量较小,miRNA 表达谱分析研究结果在不同研究之间存在不一致。我们对 20 项已发表的肺癌 miRNA 表达研究进行了全面的荟萃分析,共包括 598 个肿瘤和 528 个非癌对照样本。使用最近发表的稳健秩聚合方法,我们确定了一个具有统计学意义的 miRNA 荟萃签名,其中包括 7 个上调 miRNA(miR-21、miR-210、miR-182、miR-31、miR-200b、miR-205 和 miR-183)和 8 个下调 miRNA(miR-126-3p、miR-30a、miR-30d、miR-486-5p、miR-451a、miR-126-5p、miR-143 和 miR-145)。我们进行了基因集富集分析,以确定受这些 miRNA 表达改变影响最强烈的途径。我们发现,荟萃签名 miRNA 协同靶向信号和发育途径中功能相关和生物学相关基因。我们已经表明,这种荟萃分析方法是一种合适且有效的解决方案,通过结合几项 miRNA 表达研究来确定具有统计学意义的 miRNA 荟萃签名。该方法允许分析无法直接比较或无法获得原始数据的不同技术平台产生的数据。