Department of Physiology and Medical Physics, Royal College of Surgeons in Ireland, Dublin, Ireland; FutureNeuro, the SFI Research Centre for Chronic and Rare Neurological Diseases, Dublin, Ireland.
FutureNeuro, the SFI Research Centre for Chronic and Rare Neurological Diseases, Dublin, Ireland.
Trends Pharmacol Sci. 2021 Jul;42(7):605-616. doi: 10.1016/j.tips.2021.04.007. Epub 2021 May 12.
Epilepsy is a common and serious neurological disorder characterised by recurrent spontaneous seizures. Frontline pharmacotherapy includes small-molecule antiseizure drugs that typically target ion channels and neurotransmitter systems, but these fail in 30% of patients and do not prevent either the development or progression of epilepsy. An emerging therapeutic target is microRNA (miRNA), small noncoding RNAs that negatively regulate sets of proteins. Their multitargeting action offers unique advantages for certain forms of epilepsy with complex underlying pathophysiology, such as temporal lobe epilepsy (TLE). miRNA can be inhibited by designed antisense oligonucleotides (ASOs; e.g., antimiRs). Here, we outline the prospects for miRNA-based therapies. We review design considerations for nucleic acid-based approaches and the challenges and next steps in developing therapeutic miRNA-targeting molecules for epilepsy.
癫痫是一种常见且严重的神经系统疾病,其特征是反复发作的自发性癫痫发作。一线药物治疗包括针对离子通道和神经递质系统的小分子抗癫痫药物,但这些药物在 30%的患者中失败,并且不能预防癫痫的发展或进展。一个新兴的治疗靶点是 microRNA(miRNA),这是一种小分子非编码 RNA,可以负调控蛋白质组。它们的多靶向作用为某些具有复杂潜在病理生理学的癫痫形式(如颞叶癫痫(TLE))提供了独特的优势。miRNA 可以被设计的反义寡核苷酸(ASO;例如,antimiRs)抑制。在这里,我们概述了基于 miRNA 的治疗方法的前景。我们回顾了基于核酸的方法的设计注意事项,以及开发针对癫痫的治疗性 miRNA 靶向分子的挑战和下一步。