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Identification of differentially-expressed genes between early-stage adenocarcinoma and squamous cell carcinoma lung cancer using meta-analysis methods

机译:使用META分析方法鉴定早期腺癌和鳞状细胞癌肺癌之间的差异表达基因

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摘要

Lung adenocarcinoma (AC) and squamous cell lung carcinoma (SCC) are two major subtypes of non-small cell lung cancer (NSCLC). Previous studies have demonstrated that fundamental differences exist in the underlying mechanisms of tumor development, growth and invasion between these subtypes. The investigation of differentially-expressed genes (DEGs) between these two NSCLC subtypes is useful for determining and understanding such differences. The present study aimed to identify those DEGs using meta-analysis and the data from four microarray experiments, consisting of 164 AC and 161 SCC samples. Raw gene expression values were converted into the probability of expression (POE) representing the differentially-expressed probability of a gene and expression barcode values representing its expression status. The results indicated that when applying a meta-analysis using barcode values, heterogeneity in genes across studies was less severe than when applying a meta-analysis using POE values. DEGs in each meta-analysis method overlapped substantially (P=1.3x10(-4)), but the barcode method yielded a lower global false discovery rate. Based on this and several other performance statistics, it was concluded that the barcode approach outperformed the POE method. Finally, using those DEGs, ontology and pathway analyses vere conducted. A number of genes and enriched pathways were found to be closely associated with NSCLC.
机译:肺腺癌(AC)和鳞状细胞肺癌(SCC)是非小细胞肺癌(NSCLC)的两个主要亚型。以前的研究表明,这些亚型之间的肿瘤发育,生长和侵袭的潜在机制存在根本差异。这两个NSCLC亚型之间的差异表达基因(DEGS)的研究可用于确定和理解这种差异。本研究旨在使用Meta分析和来自四种微阵列实验的数据的DEG,由164个AC和161个SCC样品组成。将原始基因表达值转化为表示基因的差异表达概率的表达概率和表达条形码值表示其表达状态的概率。结果表明,当使用条形码值施加元分析时,在使用PoE值施加Meta分析时,基因中的基因的异质性较小。在每个META分析方法中的DEG在基本上重叠(P = 1.3×10(-4)),但条形码方法产生较低的全局假发现率。基于此和其他几个性能统计数据,得出结论,条形码方法优于PoE方法。最后,使用那些参数,本体和途径分析Vere进行。发现许多基因和富集的途径与NSCLC密切相关。

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