The mMiR-223: An inflammatory MicroRNA Involved in Pathogenesis of Multiple Sclerosis

S. Gharibi, Bahram Moghimi, M. Tahoori, M. Mahmoudi, Ensieh Shahvazian, E. F. Yazd
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引用次数: 1

Abstract

Multiple sclerosis (MS) is the most common autoimmune inflammatory demyelinating disease that affects the brain and spinal cord. Dysregulation or mutation of miRNA genes have been linked to the pathogenesis of MS. The miRNAs are short, 20-22 nucleotide long, single-stranded regulatory and non–protein coding RNAs that modulate the expression of multiple target genes. Among miRNAs, miR-223 has been reported to play a critical role in MS. This review concentrates on the emerging role of miR-223 in inflammatory responses and specifically discusses how alterations in miR-223 expression are associated with the development of MS. This review also suggests that miR-223 can be used as a biomarker for diagnosis of MS and discovering novel therapeutics for MS treatment.
mMiR-223:参与多发性硬化症发病的炎性MicroRNA
多发性硬化症(MS)是影响大脑和脊髓的最常见的自身免疫性炎症性脱髓鞘疾病。miRNA基因的失调或突变与ms的发病机制有关。miRNA是短的,长20-22个核苷酸,单链调节和非蛋白质编码rna,可调节多个靶基因的表达。在mirna中,miR-223已被报道在MS中发挥关键作用。这篇综述集中在miR-223在炎症反应中的新作用,并特别讨论了miR-223表达的改变如何与MS的发展相关。这篇综述还表明,miR-223可以用作MS诊断的生物标志物,并发现MS治疗的新疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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