Department of Anesthesiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Institute of Anesthesia and Critical Care Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Curr Med Sci. 2020 Aug;40(4):773-785. doi: 10.1007/s11596-020-2245-6. Epub 2020 Aug 29.
Renal cancer is a common genitourinary malignance, of which clear cell renal cell carcinoma (ccRCC) has high aggressiveness and leads to most cancer-related deaths. Identification of sensitive and reliable biomarkers for predicting tumorigenesis and progression has great significance in guiding the diagnosis and treatment of ccRCC. Here, we identified 2397 common differentially expressed genes (DEGs) using paired normal and tumor ccRCC tissues from GSE53757 and The Cancer Genome Atlas (TCGA). Then, we performed weighted gene co-expression network analysis and protein-protein interaction network analysis, 17 candidate hub genes were identified. These candidate hub genes were further validated in GSE36895 and Oncomine database and 14 real hub genes were identified. All the hub genes were up-regulated and significantly positively correlated with pathological stage and histologic grade of ccRCC. Survival analysis showed that the higher expression level of each hub gene tended to predict a worse clinical outcome. ROC analysis showed that all the hub genes can accurately distinguish between tumor and normal samples, and between early stage and advanced stage ccRCC. Moreover, all the hub genes were positively associated with distant metastasis, lymph node infiltration, tumor recurrence and the expression of MKi67, suggesting these genes might promote tumor proliferation, invasion and metastasis. Furthermore, the functional annotation demonstrated that most genes were enriched in cell-cycle related biological function. In summary, our study identified 14 potential biomarkers for predicting tumorigenesis and progression, which might contribute to early diagnosis, prognosis prediction and therapeutic intervention.
肾癌是一种常见的泌尿生殖系统恶性肿瘤,其中透明细胞肾细胞癌(ccRCC)侵袭性高,导致大多数与癌症相关的死亡。鉴定用于预测肿瘤发生和进展的敏感和可靠的生物标志物对于指导 ccRCC 的诊断和治疗具有重要意义。在这里,我们使用 GSE53757 和癌症基因组图谱(TCGA)中的配对正常和肿瘤 ccRCC 组织鉴定了 2397 个常见的差异表达基因(DEGs)。然后,我们进行了加权基因共表达网络分析和蛋白质-蛋白质相互作用网络分析,鉴定出 17 个候选枢纽基因。在 GSE36895 和 Oncomine 数据库中进一步验证了这些候选枢纽基因,并鉴定出 14 个真实的枢纽基因。所有的枢纽基因均上调,并与 ccRCC 的病理分期和组织学分级显著正相关。生存分析表明,每个枢纽基因的表达水平越高,临床预后越差。ROC 分析表明,所有的枢纽基因都可以准确地区分肿瘤和正常样本,以及早期和晚期 ccRCC。此外,所有的枢纽基因都与远处转移、淋巴结浸润、肿瘤复发和 MKi67 的表达呈正相关,表明这些基因可能促进肿瘤的增殖、侵袭和转移。此外,功能注释表明,大多数基因富集在细胞周期相关的生物学功能中。总之,我们的研究鉴定了 14 个潜在的用于预测肿瘤发生和进展的生物标志物,这可能有助于早期诊断、预后预测和治疗干预。