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Target genes prediction and functional analysis of microRNAs differentially expressed in gastric cancer stem cells MKN-45

机译:胃癌干细胞MKN-45中差异表达的微小RNA的靶基因预测及功能分析

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Context: Since mechanisms of microRNAs (miRNAs) in gastric cancer stem cells (CSCs) and their signaling pathways remain unknown, our aim was to predict the miRNA target genes that differentially expressed in gastric CSCs. Subjects and Methods: Using miRanda, PicTar, and TargetScan algorithm, target genes of miRNAs differentially expressed in gastric CSCs versus parental cells were predicted. Afterward, signaling pathways and biological functions of miRNAs in gastric CSCs were analyzed by the Database for Annotation, Visualization and Integrated Discovery (DAVID) database and DIANA tools. Results: Gene ontology (GO) tool indicated that most of miRNA target genes involved in regulation of cell cycle, apoptosis, cell migration, vasculogenesis, angiogenesis, etc. Some of miRNA target genes are connected to pivotal signaling pathways of the “stem cell genes,” such as Notch, Wnt/β-catenin. Conclusions: Bioinformatics analysis such as DAVID database, GO biological process, GO molecular function, Kyoto encyclopedia of genes and genomes pathways, BioCarta pathway, Panther pathway, and Reactome pathway revealed that target genes of differentially expressed miRNAs in gastric CSCs were connected to pivotal biological pathways that involved in cell cycle regulation, stemness properties, and differentiation.
机译:背景:由于胃癌干细胞(CSCs)中的microRNA(miRNA)的机制及其信号传导途径仍然未知,我们的目的是预测在胃CSCs中差异表达的miRNA靶基因。研究对象和方法:使用miRanda,PicTar和TargetScan算法,预测了在胃CSC与亲代细胞中差异表达的miRNA的靶基因。然后,通过注释,可视化和整合发现数据库(DAVID)和DIANA工具分析了胃CSC中miRNA的信号传导途径和生物学功能。结果:基因本体论(GO)工具表明,大多数miRNA靶基因都参与细胞周期,细胞凋亡,细胞迁移,血管生成,血管生成等的调控。一些miRNA靶基因与“干细胞基因”的关键信号通路相关。 ”,例如Notch,Wnt /β-catenin。结论:DAVID数据库,GO生物学过程,GO分子功能,Kyoto百科全书基因和基因组途径,BioCarta途径,Panther途径和Reactome途径等生物信息学分析表明,胃CSCs中差异表达的miRNA的靶基因与关键生物学相关。细胞周期调节,干性和分化过程中涉及的途径。

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