RNA Therapeutics: Focus on Antisense Oligonucleotides in the Nervous System

dc.contributor.authorErtural, Betul
dc.contributor.authorCicek, Busra Nur
dc.contributor.authorKurnaz, Isil Aksan
dc.date.accessioned2025-10-29T11:08:07Z
dc.date.issued2025
dc.departmentEnstitüler, Lisansüstü Eğitim Enstitüsü, Biyomühendislik Ana Bilim Dalı
dc.description.abstractRNA 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.
dc.identifier.doi10.4062/biomolther.2025.022
dc.identifier.endpage581
dc.identifier.issn1976-9148
dc.identifier.issn2005-4483
dc.identifier.issue4
dc.identifier.pmid40534528
dc.identifier.scopus2-s2.0-105010112100
dc.identifier.scopusqualityQ2
dc.identifier.startpage572
dc.identifier.urihttps://doi.org/10.4062/biomolther.2025.022
dc.identifier.urihttps://hdl.handle.net/20.500.14854/5228
dc.identifier.volume33
dc.identifier.wosWOS:001526555800002
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherKorean Soc Applied Pharmacology
dc.relation.ispartofBiomolecules & Therapeutics
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20251020
dc.subjectRNA therapeutics
dc.subjectAntisense oligonucleotides
dc.subjectASOs
dc.subjectNervous system disorders
dc.subjectDrug delivery
dc.subjectBlood brain barrier
dc.titleRNA Therapeutics: Focus on Antisense Oligonucleotides in the Nervous System
dc.typeReview Article

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