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首页> 外文期刊>European review for medical and pharmacological sciences. >Identified differently expressed genes in renal cell carcinoma by using multiple microarray datasets running head: differently expressed genes in renal cell carcinoma
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Identified differently expressed genes in renal cell carcinoma by using multiple microarray datasets running head: differently expressed genes in renal cell carcinoma

机译:使用多个微阵列数据集鉴定肾细胞癌中差异表达的基因:肾细胞癌中差异表达的基因

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OBJECTIVE: The purpose of this study was to identify differentially expressed genes and analysis biological processes related to renal cell carcinoma. METHODS: A meta-analysis was performed using the Rank Product package of Gene Expression Omnibus datasets of renal cell carcinoma. Then Gene Ontology enrichment analyses and pathway analysis were performed based on Gene Ontology website and Kyoto Encyclopedia of Genes and Genomes. Protein-protein interaction network was constructed used Cytoscape software. RESULTS: We identified a total of 1992 differentially expressed genes Rank Product package of renal cell carcinoma, 840 of them were not involved in individual DEGs. Gene Ontology enrichment analyses showed that those 840 genes enriched in terms such as response to hormone stimulus, endogenous stimulus, biological adhesion, and cell proliferation. Pathway analysis showed that significant pathways included pyruvate metabolism, glycerolipid metabolism, complement and coagulation cascades and so on. Protein-protein interaction network indicated that MT2A, MYC, CENPF and NEK2 has high degree which participated many interactions. CONCLUSIONS: Our study displayed genes that were consistently differentially expressed in renal cell carcinoma, and the biological pathways, protein-protein interaction network associated with those genes.
机译:目的:本研究旨在鉴定差异表达的基因并分析与肾细胞癌相关的生物学过程。方法:使用Gene Expression Omnibus肾细胞癌数据集的Rank Product软件包进行荟萃分析。然后根据基因本体论网站和《京都基因与基因组百科全书》进行基因本体论的富集分析和途径分析。使用Cytoscape软件构建蛋白质-蛋白质相互作用网络。结果:我们共鉴定了1992个肾细胞癌的差异表达基因Rank Product软件包,其中840个不参与单个DEG。基因本体论富集分析表明,这840个基因在对激素刺激,内源性刺激,生物粘附和细胞增殖等反应方面富集。途径分析表明,重要途径包括丙酮酸代谢,甘油脂代谢,补体和凝血级联等。蛋白质-蛋白质相互作用网络表明MT2A,MYC,CENPF和NEK2高度参与了许多相互作用。结论:我们的研究显示了在肾细胞癌中一致差异表达的基因,以及与这些基因相关的生物学途径,蛋白质-蛋白质相互作用网络。

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