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Bioinformatics Analysis Suggests the Combined Expression of AURKB and KIF18B Being an Important Event in the Development of Clear Cell Renal Cell Carcinoma

机译:生物信息学分析表明,Aurkb和KIF18B的组合表达成为透明细胞肾细胞癌发展中的重要事件

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Clear cell renal cell carcinoma (ccRCC) is the most common type of renal cell carcinoma with high metastatic rate and high mortality rate, needing to find potential therapeutic targets and develop new therapy methods. The bioinformatics analysis was used in this study to find the targets. Firstly, the expression profile of ccRCC obtained from The Cancer Genome Atlas (TCGA) database and GSE53757 dataset were used to identify the significant up-regulated genes. IL20RB, AURKB and KIF18B with the top efficiency of capable of diagnosis ccRCC from para cancer tissue, were over-expressed in ccRCC samples, and expressed increasedly with the development of ccRCC. There was the closest correlation between AURKB and KIF18B in these three over-expressed genes. AURKB (high) or KIF18B (high) were all significantly correlated with higher T, N, M stage, G grade and shorter overall survival (OS) of ccRCC patients. Furthermore, the ccRCC patients with AURKB (high) + KIF18B (high) showed worse clinical characteristics and prognosis. Multivariate COX regression analysis indicated AURKB (high) and KIF18B (high) were all the independent prognostic risk factor without considering the interaction of AURKB and KIF18B. Moreover, considering the combination of each other, only AURKB (high) + KIF18B (high) expression was an independent prognostic risk factor for ccRCC patients, but not other situations. Collectively, AURKB was closely associated with KIF18B, and the combined expression of AURKB and KIF18B may be of great significance in ccRCC.
机译:透明细胞肾细胞癌(CCRCC)是最常见的肾细胞癌,具有高转移性率和高死亡率,需要找到潜在的治疗靶点并开发新的治疗方法。在本研究中使用生物信息学分析以找到目标。首先,使用来自癌症基因组Atlas(TCGA)数据库和GSE53757数据集的CCRCC的表达谱用于鉴定显着的上调基因。 IL20RB,AurkB和KIF18B具有能够从对癌组织诊断CCRCC的效率,在CCRCC样品中过度表达,并随着CCRCC的发育而越来越多地表达。在这三种过表达基因中的Aurkb和Kif18b之间存在最近的相关性。 AURKB(高)或KIF18B(高)与CCRCC患者的较高的T,N,M阶段,G级和更短的整体存活(OS)显着相关。此外,具有Aurkb(高)+ KIF18B(高)的CCRCC患者表现出较差的临床特征和预后。多变量Cox回归分析表明Aurkb(高)和KIF18B(高)是所有独立的预后危险因素,而不考虑Aurkb和KIF18B的相互作用。此外,考虑到彼此的组合,只有Aurkb(高)+ KIF18B(高)表达是CCRCC患者的独立预后危险因素,而不是其他情况。统称,Aurkb与KIF18B密切相关,AurkB和KIF18B的组合表达在CCRCC中可能具有重要意义。

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