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Identification of key genes affecting disease free survival time of pediatric acute lymphoblastic leukemia based on bioinformatic analysis

机译:基于生物信息学分析确定影响小儿急性淋巴细胞白血病无病生存时间的关键基因

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The poor prognosis of pediatric acute lymphoblastic leukemia (ALL) indicates the existence of key candidate genes that affect pediatric ALL and its prognosis. The limma package in R was applied to screen differentially expressed genes (DEGs), and the Survival package and KMsurv package in R were used to screen disease free survival time related genes (prognosis genes). Then, based on latent pathway identification analysis (LPIA), latent pathways were identified, and pathway-pathway interaction network was constructed and visualized by Cytoscape. Based on the expression values of 8284 genes in 126 chips, 2796 DEGs and 353 prognosis genes were screened out. After overlapping DEGs and prognosis genes, 75 key genes were identified, which were most significantly enriched in 25 GO functions and chronic myeloid leukemia pathway. For the 75 key genes, 27 disease risk sub-pathways were identified, and HK3, HNMT, SULT2B1, KYNU, and PTGS2 were the significant key genes which were enriched in these sub-pathways. Furthermore, based on pathway-pathway interaction analysis, HK3 and PTGS2 were predicted as the most important genes. Through glycolysis and arachidonic acid metabolism, HK3 and PTGS2 might play important roles in pediatric ALL and its prognosis, and thus, might be potential targets for therapeutic intervention to suppress pediatric ALL (C) 2014 Elsevier Inc. All rights reserved.
机译:小儿急性淋巴细胞白血病(ALL)的预后不良表明存在影响小儿ALL及其预后的关键候选基因。 R中的limma软件包用于筛选差异表达基因(DEG),R中的Survival软件包和KMsurv软件包用于筛选无病生存时间相关基因(预后基因)。然后,基于潜在途径识别分析(LPIA),识别潜在途径,并通过Cytoscape构建途径-途径相互作用网络并可视化。根据8284个基因在126个芯片中的表达值,筛选出2796个DEG和353个预后基因。在重叠DEG和预后基因后,鉴定出75个关键基因,这些基因最显着地丰富了25个GO功能和慢性粒细胞白血病途径。对于这75个关键基因,已鉴定出27个疾病风险子途径,其中HK3,HNMT,SULT2B1,KYNU和PTGS2是在这些子途径中富集的重要关键基因。此外,基于途径-途径相互作用分析,HK3和PTGS2被预测为最重要的基因。通过糖酵解和花生四烯酸代谢,HK3和PTGS2可能在小儿ALL及其预后中起重要作用,因此可能成为抑制小儿ALL的治疗性干预措施的目标(C)2014 Elsevier Inc.保留所有权利。

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