Multiple sclerosis: The role of miRNAs and their implications in cellular pathways

IF 0.9 Q4 GENETICS & HEREDITY
Human Gene Pub Date : 2026-05-01 Epub Date: 2026-04-22 DOI:10.1016/j.humgen.2026.201562
Doha El-Sayed Ellakwa , Arwa Amer , Aya Ibrahim , Rana Aboeleneen , Al-Hassan Soliman Wadan , Takwa E. Ellakwa
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引用次数: 0

Abstract

Multiple sclerosis [MS] is a chronic autoimmune disorder characterized by inflammatory damage to the central nervous system, leading to progressive myelin degradation and neurological impairment. MicroRNAs [miRNAs] have been identified as key regulators in MS pathogenesis, with their expression being influenced by environmental, genetic, and immunological factors. Specific miRNAs, including miR-155, miR-150, and the miR-15a/16–1 cluster, are linked to dysregulated immune responses and disease progression. Moreover, the stability of miRNAs in bodily fluids positions them as potential non-invasive biomarkers for MS diagnosis. However, despite these advancements, MS remains a complex condition that is challenging to diagnose and treat effectively. The heterogeneity of the disease and the intricate regulatory mechanisms governing miRNA expression present significant barriers to the development of targeted therapies and reliable biomarkers. This review examines the diverse functions of miRNAs in MS, emphasizing their dual role as biomarkers and therapeutic targets. It discusses the distinct miRNA expression profiles identified in the serum and cerebrospinal fluid of MS patients, which may contribute to improved diagnostic precision. Additionally, advancements in miRNA delivery and modulation technologies are explored as promising therapeutic strategies to restore immune balance and reduce neuroinflammation. By harnessing these insights, researchers may refine diagnostic tools and develop targeted treatments, ultimately enhancing clinical outcomes for MS patients. This review highlights the necessity for further investigation into miRNA-based approaches, advocating for continued research to fully realize their potential in advancing MS diagnosis and therapeutic strategies.
多发性硬化症:mirna的作用及其在细胞通路中的意义
多发性硬化症(MS)是一种慢性自身免疫性疾病,其特征是中枢神经系统的炎症性损伤,导致髓磷脂进行性降解和神经功能障碍。MicroRNAs [miRNAs]已被确定为MS发病的关键调节因子,其表达受环境、遗传和免疫因素的影响。特异性mirna,包括miR-155、miR-150和miR-15a/ 16-1簇,与失调的免疫反应和疾病进展有关。此外,体液中mirna的稳定性使其成为MS诊断的潜在非侵入性生物标志物。然而,尽管取得了这些进展,多发性硬化症仍然是一种复杂的疾病,很难有效地诊断和治疗。该疾病的异质性和控制miRNA表达的复杂调控机制对靶向治疗和可靠生物标志物的开发构成了重大障碍。本文综述了microrna在多发性硬化症中的多种功能,强调了它们作为生物标志物和治疗靶点的双重作用。它讨论了在MS患者的血清和脑脊液中鉴定的不同miRNA表达谱,这可能有助于提高诊断精度。此外,miRNA传递和调节技术的进步被认为是恢复免疫平衡和减少神经炎症的有希望的治疗策略。通过利用这些见解,研究人员可以改进诊断工具并开发有针对性的治疗方法,最终提高多发性硬化症患者的临床疗效。这篇综述强调了进一步研究基于mirna的方法的必要性,提倡继续研究以充分发挥其在推进MS诊断和治疗策略方面的潜力。
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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来源期刊
Human Gene
Human Gene Biochemistry, Genetics and Molecular Biology (General), Genetics
CiteScore
1.60
自引率
0.00%
发文量
0
审稿时长
54 days
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