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Transcriptomic analysis delineates potential signature genes and miRNAs associated with the pathogenesis of asthma

机译:转录组分析描绘了与哮喘发病机制相关的潜在签名基因和miRNA

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Asthma is a multifarious disease affecting several million people around the world. It has a heterogeneous risk architecture inclusive of both genetic and environmental factors. This heterogeneity can be utilised to identify differentially expressed biomarkers of the disease, which may ultimately aid in the development of more localized and molecularly targeted therapies. In this respect, our study complies with meta-analysis of microarray datasets containing mRNA expression profiles of both asthmatic and control patients, to identify the critical Differentially Expressed Genes (DEGs) involved in the pathogenesis of asthma. We found a total of 30 DEGs out of which 13 were involved in the pathway and functional enrichment analysis. Moreover, 5 DEGs were identified as the hub genes by network centrality-based analysis. Most hub genes were involved in protease/antiprotease pathways. Also, 26 miRNAs and 20 TFs having an association with these hub genes were found to be intricated in a 3-node miRNA Feed-Forward Loop. Out of these, miR-34b and miR-449c were identified as the key miRNAs regulating the expression of SERPINB2 gene and SMAD4 transcription factor. Thus, our study is suggestive of certain miRNAs and unexplored pathways which may pave a way to unravel critical therapeutic targets in asthma.
机译:哮喘是一种影响世界各地数百万人的多种疾病。它具有包含遗传和环境因素的异质风险架构。这种异质性可用于鉴定疾病的差异表达的生物标志物,这可能最终有助于开发更局部和分子靶向疗法。在这方面,我们的研究符合含有哮喘和对照患者的mRNA表达谱的微阵列数据集的荟萃分析,以鉴定患有哮喘发病机制的临界差异表达基因(DEGS)。我们发现总共30次,其中13次涉及途径和功能性富集分析。此外,通过基于网络中心的分析鉴定为中心基因的5次。大多数轮毂基因参与蛋白酶/抗滴油性途径。此外,发现与这些轮毂基因相关的26 mIRNA和20 TFS在3节点miRNA馈送环中复杂。除此之外,MiR-34B和MIR-449C被鉴定为调节SerpinB2基因和Smad4转录因子的表达的关键miRNA。因此,我们的研究表达了某些MiRNA和未探究的途径,这可能会铺平哮喘危害临界治疗靶标的方法。

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