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Identification of hsa-miR-1275 as a Novel Biomarker Targeting MECP2 for Human Epilepsy of Unknown Etiology

机译:鉴定HSA-miR-1275作为靶向MECP2的新型生物标志物,用于未知病因的人癫痫

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Epilepsy affects around 70 million people worldwide, with a 65% rate of unknown etiology. This rate is known as epilepsy of unknown etiology (EUE). Dysregulation of microRNAs (miRNAs) is recognized to contribute to mental disorders, including epilepsy. However, miRNA dysregulation is poorly understood in EUE. Here, we conducted miRNA expression profiling of EUE by microarray technology and identified 57 pathogenic changed miRNAs with significance. The data and bioinformatic analysis results indicated that among these miRNAs, hsa-microRNA (miR)-1275 was highly associated with neurological disorders. Subsequently, new samples of serum and cerebrospinal fluid were collected for validation of hsa-miR-1275 expression by TaqMan assays. Results show that hsa-miR-1275 in serums of EUE were increased significantly, but in cerebrospinal fluid, the miRNA was decreased. Moreover, the MECP2 gene was selected as a hsa-miR-1275 target based on target prediction tools and gene ontology analysis. Validation of in?vitro tests proved that MECP2 expression was specifically inhibited by hsa-miR-1275. Additionally, overexpression of hsa-miR-1275 can elevate expression of nuclear factor κB (NF-κB) and promote cell apoptosis. Taken together, hsa-miR-1275 might represent a novel biomarker targeting MECP2 for human EUE.
机译:癫痫影响全世界约有7000万人,未知病因的65%。此速率被称为未知病因(EUE)的癫痫。 MicroRNAS的失调(MIRNA)被认识到为患有精神障碍有助于包括癫痫。然而,MiRNA失呼算法在EUE中明显不知情。在这里,我们通过微阵列技术进行了MiRNA表达分析,并确定了具有重要意义的57种致病性的miRNA。数据和生物信息分析结果表明,在这些miRNA中,HSA-microRNA(miR)-1275与神经系统疾病高度相关。随后,收集新的血清和脑脊液样品以通过Taqman测定验证HSA-miR-1275表达。结果表明,随着脑脊液中血清血清中的HSA-MIR-1275增加,但在脑脊液中,miRNA降低。此外,基于目标预测工具和基因本体分析,选择MECP2基因作为HSA-miR-1275靶。验证体外试验证明,MECP2表达被HSA-miR-1275特异性抑制。另外,HSA-MIR-1275的过表达可以提高核因子κB(NF-κB)的表达,促进细胞凋亡。占据,HSA-MIR-1275可能代表一个针对人类州的MECP2的新型生物标志物。

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