共表达网络分析发现6个枢纽基因与人透明细胞肾细胞癌(ccRCC)的进展和预后相关

Lushun Yuan , Liang Chen , Kaiyu Qian , Guofeng Qian , Chin-Lee Wu , Xinghuan Wang , Yu Xiao
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引用次数: 74

摘要

人透明细胞肾细胞癌(ccRCC)是最常见的成人肾恶性肿瘤之一。我们构建了一个加权基因共表达网络来识别与ccRCC临床特征相关的基因模块(n = 97)。CCNB2、CDC20、CEP55、KIF20A、TOP2A和UBE2C 6个枢纽基因在共表达和蛋白-蛋白相互作用(PPI)网络中均存在,且与病理分期高度相关。枢纽基因在ccRCC中表达的意义在所有肿瘤中排名前4,且与预后不良相关。功能分析显示,中枢基因在细胞周期调控和细胞分裂中显著富集。基因集富集分析表明hub基因高表达的样品与细胞周期和p53信号通路相关。综上所述,我们发现6个中枢基因与ccRCC的进展和预后相关,它们可能通过调节p53信号通路导致预后不良。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Co-expression network analysis identified six hub genes in association with progression and prognosis in human clear cell renal cell carcinoma (ccRCC)

Co-expression network analysis identified six hub genes in association with progression and prognosis in human clear cell renal cell carcinoma (ccRCC)

Co-expression network analysis identified six hub genes in association with progression and prognosis in human clear cell renal cell carcinoma (ccRCC)

Co-expression network analysis identified six hub genes in association with progression and prognosis in human clear cell renal cell carcinoma (ccRCC)

Human clear cell renal cell carcinoma (ccRCC) is one of the most common types of malignant adult kidney tumors. We constructed a weighted gene co-expression network to identify gene modules associated with clinical features of ccRCC (n = 97). Six hub genes (CCNB2, CDC20, CEP55, KIF20A, TOP2A and UBE2C) were identified in both co-expression and protein-protein interaction (PPI) networks, which were highly correlated with pathologic stage. The significance of expression of the hub genes in ccRCC was ranked top 4 among all cancers and correlated with poor prognosis. Functional analysis revealed that the hub genes were significantly enriched in cell cycle regulation and cell division. Gene set enrichment analysis suggested that the samples with highly expressed hub gene were correlated with cell cycle and p53 signaling pathway. Taken together, six hub genes were identified to be associated with progression and prognosis of ccRCC, and they might lead to poor prognosis by regulating p53 signaling pathway.

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