RNA Therapeutics: Focus on Antisense Oligonucleotides in the Nervous System.

IF 3.2 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Biomolecules & Therapeutics Pub Date : 2025-07-01 Epub Date: 2025-06-19 DOI:10.4062/biomolther.2025.022
Betül Ertural, Büşra Nur Çiçek, Işıl Aksan Kurnaz
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引用次数: 0

Abstract

RNA therapeutics represent a disruptive technology that has transformed drug discovery and manufacturing, gaining significant prominence during the COVID-19 pandemic. RNA therapeutics encompass diverse molecules like antisense oligonucleotides (ASOs), small interfering RNAs (siRNAs), microRNAs (miRNAs), RNA aptamers, and messenger RNAs (mRNAs), which can function through different mechanisms. RNA therapeutics are increasingly used to treat various diseases, including neurological disorders. For example, ASO therapies such as nusinersen for spinal muscular atrophy and eteplirsen for Duchenne muscular dystrophy are successful applications of RNA-based treatment. Emerging ASO treatments for Huntington's disease and amyotrophic lateral sclerosis are also promising, with ongoing clinical trials demonstrating significant reductions in disease-associated proteins. Still, delivery of these molecules remains a pivotal challenge in RNA therapeutics, especially for ASOs in penetrating the blood-brain barrier to target neurological disorders effectively. Nanoparticle-based formulations have emerged as leading strategies to enhance RNA stability, reduce immunogenicity, and improve cellular uptake. Despite these advances, significant hurdles remain, including optimizing pharmacokinetics, minimizing off-target effects, and ensuring sustained therapeutic efficacy. Regulatory frameworks are evolving to accommodate the unique challenges of RNA-based therapies, including ASOs with efforts underway to establish comprehensive guidelines for RNA therapeutics, yet there are also sustainable manufacturing issues that need to be considered for long-term feasibility. By addressing these challenges, RNA therapeutics hold immense potential to revolutionize treatment paradigms for neurological disorders. Looking forward, the future of RNA therapeutics in neurology appears promising but requires continued interdisciplinary collaboration and technological innovation.

RNA治疗:关注神经系统中的反义寡核苷酸。
RNA疗法是一种颠覆性的技术,它改变了药物发现和制造的格局,在最近的COVID-19大流行中,这种格局更加突出。RNA疗法包括反义寡核苷酸(ASOs)、小干扰RNA (sirna)、微RNA (miRNAs)、RNA适体和信使RNA (mrna)等多种分子,它们可以通过不同的机制发挥作用。RNA疗法在一系列疾病中的应用正在扩大,特别是在神经系统疾病的治疗中。例如,治疗脊髓性肌萎缩症的nusinersen和治疗杜氏肌营养不良症的eteplirsen等ASO疗法就是成功的RNA治疗策略的例子。新兴的ASO治疗亨廷顿氏病和肌萎缩侧索硬化症也很有希望,正在进行的临床试验表明,疾病相关蛋白的显著减少。尽管如此,这些分子的递送仍然是RNA治疗的关键挑战,特别是对于ASOs穿透血脑屏障以有效靶向神经系统疾病。基于纳米颗粒的配方已经成为增强RNA稳定性、降低免疫原性和改善细胞摄取的主要策略。尽管取得了这些进展,但仍存在重大障碍,包括优化药代动力学,最大限度地减少脱靶效应,并确保持续的治疗效果。监管框架正在不断发展,以适应基于RNA治疗的独特挑战,包括正在努力建立RNA治疗综合指南的aso,但也存在可持续生产问题,需要考虑长期可行性。通过解决这些挑战,RNA疗法具有巨大的潜力,可以彻底改变神经系统疾病的治疗模式。展望未来,RNA疗法在神经病学中的应用前景广阔,但仍需要持续的跨学科合作和技术创新。
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
CiteScore
6.60
自引率
8.10%
发文量
72
审稿时长
6-12 weeks
期刊介绍: Biomolecules & Therapeutics (Biomolecules & Therapeutics) (Print ISSN 1976-9148, Online ISSN 2005-4483) is an international, peer-reviewed, open access journal that covers pharmacological and toxicological fields related to bioactive molecules and therapeutics. It was launched in 1993 as "The Journal of Applied Pharmacology (ISSN 1225-6110)", and renamed "Biomolecules & Therapeutics" (Biomol Ther: abbreviated form) in 2008 (Volume 16, No. 1). It is published bimonthly in January, March, May, July, September and November. All manuscripts should be creative, informative, and contribute to the development of new drugs. Articles in the following categories are published: review articles and research articles.
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