The therapeutic potential of siRNA in gene therapy of neurodegenerative disorders.

E Koutsilieri, A Rethwilm, C Scheller
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引用次数: 52

Abstract

RNA interference using small inhibitory RNA (siRNA) has become a powerful tool to downregulate mRNA levels by cellular nucleases that become activated when a sequence homology between the siRNA and a respective mRNA molecule is detected. Therefore siRNA can be used to silence genes involved in the pathogenesis of various diseases associated with a known genetic background. As for many neurodegenerative disorders a causative therapy is unavailable, siRNA holds a promising option for the development of novel therapeutic strategies. Here we discuss different siRNA target strategies aiming for an allele-specific degradation of disease-inducing mRNA and we review the literature in the field of siRNA and its application in animal models of neurodegenerative diseases, including Alzheimer's disease (AD), amyotrophic lateral sclerosis (ALS), Huntington's disease (HD) and spinocerebellar ataxia (SCA1).

siRNA在神经退行性疾病基因治疗中的治疗潜力。
使用小抑制RNA (siRNA)进行RNA干扰已经成为下调mRNA水平的有力工具,当检测到siRNA和相应mRNA分子之间的序列同源性时,细胞核酸酶会被激活。因此,siRNA可用于沉默与已知遗传背景相关的各种疾病发病机制相关的基因。由于许多神经退行性疾病没有病因治疗,siRNA为开发新的治疗策略提供了一个有希望的选择。在这里,我们讨论了不同的siRNA靶向策略,旨在等位基因特异性降解疾病诱导mRNA,并回顾了siRNA领域的文献及其在神经退行性疾病动物模型中的应用,包括阿尔茨海默病(AD)、肌萎缩性侧索硬化症(ALS)、亨廷顿病(HD)和脊髓小脑性共济失调(SCA1)。
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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