Department of Colorectal Surgery, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou 310016, China.
Department of Oral Implantology and Prosthodontics, The Affiliated Stomatology Hospital, Zhejiang University School of Medicine, Hangzhou 310006, China.
Biomed Res Int. 2020 Mar 28;2020:2137319. doi: 10.1155/2020/2137319. eCollection 2020.
Clear cell renal cell carcinoma (ccRCC) is a major histological subtype of renal cell carcinoma and can be clinically divided into four stages according to the TNM criteria. Identifying clinical stage-related genes is beneficial for improving the early diagnosis and prognosis of ccRCC. By using bioinformatics analysis, we aim to identify clinical stage-relevant genes that are significantly associated with the development of ccRCC. First, we analyzed the gene expression microarray data sets: GSE53757 and GSE73731. We divided these data into five groups by staging information-normal tissue and ccRCC stages I, II, III, and IV-and eventually identified 500 differentially expressed genes (DEGs). To obtain precise stage-relevant genes, we subsequently applied weighted gene coexpression network analysis (WGCNA) to the GSE73731 dataset and KIRC data from The Cancer Genome Atlas (TCGA). Two modules from each dataset were identified to be related to the tumor TNM stage. Several genes with high inner connection inside the modules were considered hub genes. The intersection results between hub genes of key modules and 500 DEGs revealed UBE2C, BUB1B, RRM2, and TPX2 as highly associated with the stage of ccRCC. In addition, the candidate genes were validated at both the RNA expression level and the protein level. Survival analysis also showed that 4 genes were significantly correlated with overall survival. In conclusion, our study affords a deeper understanding of the molecular mechanisms associated with the development of ccRCC and provides potential biomarkers for early diagnosis and individualized treatment for patients at different stages of ccRCC.
透明细胞肾细胞癌(ccRCC)是肾细胞癌的主要组织学亚型,可根据 TNM 标准临床分为四期。鉴定与临床分期相关的基因有助于提高 ccRCC 的早期诊断和预后。通过使用生物信息学分析,我们旨在鉴定与 ccRCC 发生发展显著相关的临床分期相关基因。首先,我们分析了基因表达微阵列数据集:GSE53757 和 GSE73731。我们根据分期信息-正常组织和 ccRCC Ⅰ期、Ⅱ期、Ⅲ期和Ⅳ期-将这些数据分为五组,最终确定了 500 个差异表达基因(DEGs)。为了获得更精确的分期相关基因,我们随后应用加权基因共表达网络分析(WGCNA)对 GSE73731 数据集和 TCGA 中的 KIRC 数据进行分析。从每个数据集识别到两个与肿瘤 TNM 分期相关的模块。模块内具有高内部连接的几个基因被认为是枢纽基因。关键模块的枢纽基因与 500 个 DEGs 的交集结果揭示 UBE2C、BUB1B、RRM2 和 TPX2 与 ccRCC 的分期高度相关。此外,候选基因在 RNA 表达水平和蛋白质水平上均得到验证。生存分析还表明,4 个基因与总生存率显著相关。总之,我们的研究深入了解了与 ccRCC 发生发展相关的分子机制,并为不同分期的 ccRCC 患者的早期诊断和个体化治疗提供了潜在的生物标志物。