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miRNA expression analysis in cortical dysplasia: regulation of mTOR and LIS1 pathway.

机译:皮质发育异常中的miRNA表达分析:调节mTOR和LIS1途径。

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Cortical dysplasia (CD) is a common cause of epilepsy in children and is characterized by focal regions of malformed cerebral cortex. The pathogenesis and epileptogenesis of CD have not been fully elucidated, and in particular, the potential role of epigenetics has not been examined. miRNA microarray was performed on surgical specimens from CD (n=8) and normal control (n=2) children. A total of 10 differentially expressed miRNAs (DEmiRs) that were up-regulated in CD were identified including hsa-miR-21 and hsa-miR-155. The microarray results were validated using quantitative real-time PCR. After searching for the putative target genes of the DEmiRs, their biological significance was further evaluated by exploring the pathways in which the genes were enriched. The mammalian target of rapamycin (mTOR) signaling pathway was the most significantly associated, and the pathway of lissencephaly gene in neuronal migration and development was also noted. This study suggests a possible role for miRNAs in the pathogenesis of CD, especially in relation to the mTOR signaling pathway. Future studies on the epigenetic mechanisms underlying CD pathogenesis and epileptogenesis are needed.
机译:皮质发育不良(CD)是儿童癫痫的常见病因,其特征是畸形的大脑皮层的局灶性区域。 CD的发病机理和癫痫发生尚未完全阐明,尤其是表观遗传学的潜在作用尚未得到检验。对来自CD(n = 8)和正常对照(n = 2)儿童的手术标本进行了miRNA芯片分析。总共鉴定出10种在CD中上调的差异表达的miRNA(DEmiR),包括hsa-miR-21和hsa-miR-155。使用定量实时PCR验证了微阵列结果。在寻找DEmiRs的假定靶基因后,通过探索富集基因的途径进一步评估了它们的生物学意义。雷帕霉素(mTOR)信号转导通路的哺乳动物目标是最显着相关,并且还提到了lissencephaly基因在神经元迁移和发育中的通路。这项研究表明,miRNA在CD的发病机制中可能具有重要作用,特别是与mTOR信号通路有关。需要对CD发病机制和癫痫发生的表观遗传机制进行进一步的研究。

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