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Reconstruction of the lncRNA-miRNA-mRNA network based on competitive endogenous RNA reveal functional lncRNAs in Cerebral Infarction

机译:基于竞争性内源RNA的lncRNA-miRNA-mRNA网络的重建揭示了脑梗死中的功能性nccRNA

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摘要

Functioning as miRNA sponges, long non-coding RNA (lncRNA) exert its pharmacological action via regulating expression of protein-coding genes. However, the lncRNA-mediated ceRNA in cerebral Infarction (CI) remains unclear. In this study, the expression recordsets of mRNA, lncRNA and miRNA of CI samples were obtained from the NCBI GEO datasets separately. The differentially expressed lncRNAs (DELs), miRNAs (DEMis) and mRNAs (DEMs) were identified by limma package in R platform. A total of 267 DELs, 26 DEMis, and 760 DEMs were identified as differentially expressed profiles, with which we constructed the ceRNA network composed of DELs-DEMis-DEMs. Further, clusterProfiler package in R platform is employed for performing Gene Ontology (GO) and KEGG pathway analysis. An aberrant ceRNA network was constructed according to node degrees in CI, including 28 DELs, 19 DEMs and 12 DEMis, from which we extracted the core network, in which 9 nodes were recognized as kernel genes including Tspan3, Eif4a2, rno-miR-208a-3p, rno-miR-194-5p, Pdpn, H3f3b, Stat3, Cd63 and Sdc4. Finally, with the DELs-DEMis-DEMs ceRNA network provided above, we can improve our understanding of the pathogenesis of CI mediated by lncRNA.
机译:长的非编码RNA(lncRNA)充当miRNA海绵,通过调节蛋白质编码基因的表达发挥其药理作用。但是,尚不清楚lncRNA介导的ceRNA在脑梗死(CI)中的作用。本研究分别从NCBI GEO数据集获得CI样品的mRNA,lncRNA和miRNA的表达记录集。通过limma程序包在R平台中鉴定出差异表达的lncRNA(DEL),miRNA(DEMis)和mRNA(DEM)。共有267个DEL,26个DEMis和760个DEM被鉴定为差异表达谱,我们用它们构建了由DELs-DEMis-DEM组成的ceRNA网络。此外,R平台中的clusterProfiler软件包用于执行基因本体论(GO)和KEGG途径分析。根据CI中的节点度构建了异常的ceRNA网络,包括28个DEL,19个DEM和12个DEMi,我们从中提取了核心网络,其中9个节点被识别为包括Tspan3,Eif4a2,rno-miR-208a在内的核心基因。 -3p,rno-miR-194-5p,Pdpn,H3f3b,Stat3,Cd63和Sdc4。最后,借助上面提供的DELs-DEMis-DEMs ceRNA网络,我们可以增进对lncRNA介导的CI发病机制的了解。

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