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Analysis of altered microRNA expression profile in the reparative interface of the femoral head with osteonecrosis

机译:股骨头坏死股骨头修复界面微RNA表达谱变化的分析

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The reparative reaction is considered to be important during the occurrence of collapse in the femoral head with osteonecrosis (ONFH), but little is known about the long-term reparative process. The aim of this study was to determine and analyze the altered microRNA expression profile in the reparative interface of ONFH, and further validate the expression of the involved genes in the predicted pathways. Microarray analysis was performed comparing the reparative interface of patients with ONFH and normal tissue of patients with fresh femoral neck fracture (FNF) and partly validated by real-time PCR. Potential target genes of differentially expressed miRNAs were predicted by TargetScan and miRanda, and the target genes were used for further bioinformatics analysis such as Gene Ontology and Pathway assay. The filtered miRNAs and genes in the predict pathways were further examined by real-time PCR in another 6 independent ONFH patients. Among the 2578 miRNAs identified, 17 were consistently differentially expressed, 12 of which are up-regulated and 5 down-regulated. GO classification showed that the predicted target genes of these miRNAs are involved in signal transduction, cell differentiation, methylation, cell growth and apoptosis. The Kyoto Encyclopedia of Genes and Genomes (KEGG) classification indicated that these genes play a role in angiogenesis and Wnt signaling pathways. The expression of miR-34a and miR-146a and genes in the predict pathways were significantly up-regulated. This study presented a global view of miRNA expression in the reparative interface of osteonecrosis. In addition, our data provided novel and robust information for further researches in the pathogenesis and molecular events of ONFH. (C) 2015 Elsevier Inc. All rights reserved.
机译:在发生股骨头坏死(ONFH)的股骨头塌陷期间,修复反应被认为是重要的,但长期修复过程知之甚少。这项研究的目的是确定和分析ONFH修复界面中microRNA表达谱的改变,并进一步验证所预测途径中涉及基因的表达。进行了微阵列分析,比较了ONFH患者和新鲜股骨颈骨折(FNF)患者的正常组织的修复界面,并通过实时PCR进行了部分验证。通过TargetScan和miRanda预测了差异表达的miRNA的潜在靶基因,并将该靶基因用于进一步的生物信息学分析,如基因本体论和通路分析。通过实时PCR在另外6名独立的ONFH患者中进一步检查了预测途径中的过滤miRNA和基因。在鉴定出的2578个miRNA中,有17个一致地差异表达,其中12个上调而5个下调。 GO分类显示,这些miRNA的预测靶基因与信号转导,细胞分化,甲基化,细胞生长和凋亡有关。 《京都议定书》的基因和基因组百科全书(KEGG)分类表明,这些基因在血管生成和Wnt信号通路中起作用。 miR-34a和miR-146a的表达以及预测通路中的基因均显着上调。这项研究提出了骨坏死修复界面中的miRNA表达的全局视图。此外,我们的数据为ONFH的发病机理和分子事件的进一步研究提供了新颖而可靠的信息。 (C)2015 Elsevier Inc.保留所有权利。

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