Sun Bingqing, Zhao Hongwen
Department of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of China Medical University, Shenyang, China.
Cancer Inform. 2022 Mar 22;21:11769351221082020. doi: 10.1177/11769351221082020. eCollection 2022.
To investigate the differential expression of genes and microRNAs (miRNAs) in patients with lung adenocarcinoma and the relationship between such changes and patient prognosis.
We analyzed the expression levels of genes and miRNAs in lung adenocarcinoma tissues and adjacent normal tissues using The Cancer Genome Atlas database (TCGA). We analyzed the function of the differentially expressed genes and miRNAs in a co-expression network. Finally, we performed survival analysis of differential genes and miRNAs in the co-expression network using clinical data from the TCGA database.
We successfully identified 6064 differentially expressed genes: 5324 upregulated genes and 740 downregulated genes. And we identified 161 differentially expressed miRNAs: 126 upregulated miRNAs and 35 downregulated miRNAs. We identified several genes that were related to each other in the co-expression network. Further analysis revealed that the high expression levels of , and genes were associated with poor prognosis. However, there was no significant correlation between the expression of with regards to patient prognosis.
Our data showed that and a number of related genes may affect the prognosis of patients with lung adenocarcinoma by regulating the cytoskeleton, thus promoting tumor angiogenesis and the metastasis of tumor cells. The high expression levels of some differentially expressed genes was associated with the low survival rate in patients with lung adenocarcinoma. However, the levels of were not correlated with patient prognosis.
研究肺腺癌患者中基因和微小RNA(miRNA)的差异表达,以及这些变化与患者预后的关系。
我们使用癌症基因组图谱数据库(TCGA)分析了肺腺癌组织和邻近正常组织中基因和miRNA的表达水平。我们在共表达网络中分析了差异表达基因和miRNA的功能。最后,我们使用TCGA数据库的临床数据对共表达网络中的差异基因和miRNA进行了生存分析。
我们成功鉴定出6064个差异表达基因:5324个上调基因和740个下调基因。我们还鉴定出161个差异表达的miRNA:126个上调的miRNA和35个下调的miRNA。我们在共表达网络中鉴定出了几个相互关联的基因。进一步分析表明, 、 和 基因的高表达与预后不良相关。然而, 基因的表达与患者预后之间没有显著相关性。
我们的数据表明, 及一些相关基因可能通过调节细胞骨架影响肺腺癌患者的预后,从而促进肿瘤血管生成和肿瘤细胞转移。一些差异表达基因的高表达与肺腺癌患者的低生存率相关。然而, 基因的水平与患者预后无关。