Gu Yanqin, Lu Linfeng, Wu Lingfeng, Chen Hao, Zhu Wei, He Yi
Department of Urology, The First Hospital of Jiaxing, Jiaxing, Zhejiang 314001, P.R. China.
Mol Med Rep. 2017 Apr;15(4):1661-1667. doi: 10.3892/mmr.2017.6194. Epub 2017 Feb 13.
The present study aimed to analyze RNA-seq data of kidney renal clear cell carcinoma (KIRC) to identify prognostic genes. RNA‑seq data were downloaded from The Cancer Genome Atlas. Feature genes with a coefficient of variation (CV) >0.5 were selected using the genefilter package in R. Gene co‑expression networks were constructed with the WGCNA package. Cox regression analysis was performed using the survive package. Furthermore, a functional enrichment analysis was conducted using Database for Annotation, Visualization and Integrated Discovery tools. A total of 533 KIRC samples were collected, from which 6,758 feature genes with a CV >0.5 were obtained for further analysis. The KIRC samples were divided into two sets: The training set (n=319 samples) and the validation set (n=214 samples). Subsequently, gene co‑expression networks were constructed for the two sets. A total of 12 modules were identified, and the green module was significantly associated with survival time. Genes from the green module were revealed to be implicated in the cell cycle and p53 signaling pathway. In addition, a total of 11 hub genes were revealed, and 10 of them (CCNA2, CDC20, CDCA8, GTSE1, KIF23, KIF2C, KIF4A, MELK, TOP2A and TPX2) were validated as possessing prognostic value, as determined by conducting a survival analysis on another gene expression dataset. In conclusion, a total of 10 prognostic genes were identified in KIRC. These findings may help to advance the understanding of this disease, and may also provide potential biomarkers for therapeutic development.
本研究旨在分析肾透明细胞癌(KIRC)的RNA测序数据,以鉴定预后基因。RNA测序数据从癌症基因组图谱下载。使用R语言中的genefilter包选择变异系数(CV)>0.5的特征基因。用WGCNA包构建基因共表达网络。使用survive包进行Cox回归分析。此外,使用注释、可视化和综合发现数据库工具进行功能富集分析。共收集了533个KIRC样本,从中获得6758个CV>0.5的特征基因用于进一步分析。将KIRC样本分为两组:训练集(n = 319个样本)和验证集(n = 214个样本)。随后,为这两组构建基因共表达网络。共鉴定出12个模块,绿色模块与生存时间显著相关。绿色模块中的基因被发现与细胞周期和p53信号通路有关。此外,共发现11个枢纽基因,其中10个(CCNA2、CDC20、CDCA8、GTSE1、KIF23、KIF2C、KIF4A、MELK、TOP2A和TPX2)经对另一个基因表达数据集进行生存分析确定具有预后价值。总之,在KIRC中鉴定出了10个预后基因。这些发现可能有助于增进对这种疾病的了解,也可能为治疗开发提供潜在的生物标志物。