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Identification of miRNA and genes involving in osteosarcoma by comprehensive analysis of microRNA and copy number variation data

机译:通过微罗纳和拷贝数变异数据综合分析鉴定涉及骨肉瘤的miRNA和基因

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The aim of the present study was to understand the molecular mechanisms of osteosarcoma by comprehensive analysis of microRNA (miRNA/ miR) and copy number variation (CNV) microarray data. Microarray data (GSE65071 and GSE33153) were downloaded from the Gene Expression Omnibus. In GSE65071, differentially expressed miRNAs between the osteosarcoma and control groups were calculated by the Limma package. Target genes of differentially expressed miRNAs were identified by the starBase database. For GSE33153, PennCNV software was used to perform the copy number variation (CNV) analysis. Overlapping of the genes in CNV regions and the target genes of differentially expressed miRNAs were used to construct miRNA-gene regulatory network using the starBase database. A total of 149 differentially expressed miRNAs, including 13 downregulated and 136 upregulated, were identified. In the GSE33153 dataset, 987 CNV regions involving in 3,635 genes were identified. In total, 761 overlapping genes in 987 CNV regions and in the genes in 7,313 miRNA-gene pairs were obtained. miRNAs (hsa-miR-27a-3p, hsa-miR-124-3p, hsa-miR-9-5p, hsa-miR-182-5p, hsa-miR-26a-5p) and the genes [Fibroblast growth factor receptor substrate 2 (FRS2), coronin 1C (CORO1C), forkhead box P1 (FOXP1), cytoplasmic polyadenylation element binding protein 4 (CPEB4) and glucocorticoid induced 1 (GLCCI1)] with the highest degrees of association with osteosarcoma development were identified. Hsa-miR-27a-3p, hsa-miR-9-5p, hsa-miR-182-5p, FRS2, CORO1C, FOXP1 and CPEB4 may be involved in osteosarcoma pathogenesis, and development.
机译:本研究的目的是通过综合分析MicroRNA(miRNA / miR)和拷贝数变异(CNV)微阵列数据来了解骨肉瘤的分子机制。从基因表达综合症下载微阵列数据(GSE65071和GSE33153)。在GSE65071中,通过雷玛包计算骨肉瘤和对照组之间的差异表达的miRNA。 Starbase数据库鉴定了差异表达miRNA的靶基因。对于GSE33153,PennCNV软件用于执行副本数变型(CNV)分析。使用Starbase数据库使用STARBASE数据库来构建MiRNA-基因调节网络的CNV区内基因和差异表达的miRNA的靶基因的重叠。鉴定了总共149个差异表达的miRNA,包括下调和136个上调,上调。在GSE33153数据集中,确定了涉及3,635个基因的987个CNV区域。在987个CNV地区和7,313个miRNA-基因对中的基因中总共761个重叠基因。 miRNA(HSA-MIR-27A-3P,HSA-MIR-124-3P,HSA-MIR-9-5P,HSA-MIR-182-5P,HSA-MIR-26A-5P)和基因[成纤维细胞生长因子受体鉴定了衬底2(FRS2),冠状蛋白1C(Coro1C),叉头盒P1(FoxP1),细胞质多腺苷酸化元素结合蛋白4(CPEB4)和糖皮质激素诱导的1(GLCCI1)与与骨肉瘤发育的最高结合进行了诱导的1(GLCCI1)。 HSA-MIR-27A-3P,HSA-MIR-9-5P,HSA-MIR-182-5P,FRS2,CORO1C,FOXP1和CPEB4可参与骨肉瘤发病机制和发育。

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