DNAzymes:扩大核酸治疗的潜力。

IF 4 2区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Leon M Larcher, Ianthe L Pitout, Niall P Keegan, Rakesh N Veedu, Sue Fletcher
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引用次数: 1

摘要

核酸药物已被临床证明是治疗遗传和获得性疾病的有力手段。然而,包括药物稳定性、肾脏清除率、细胞摄取和跨越生物屏障(主要是血脑屏障)的运动在内的关键挑战限制了基于核酸的疗法在全身和中枢神经系统中的转化和临床疗效。在这项研究中,我们提供了一个新兴的一类核酸治疗的概述,称为DNAzymes。特别地,我们回顾了在细胞和动物模型中使用化学修饰和载体分子来稳定和/或递送DNAzymes。虽然本综述侧重于DNAzymes,但所描述的策略广泛适用于大多数核酸技术。本文综述可作为选择化学修饰以提高DNAzymes治疗性能的一般指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

DNAzymes: Expanding the Potential of Nucleic Acid Therapeutics.

DNAzymes: Expanding the Potential of Nucleic Acid Therapeutics.

DNAzymes: Expanding the Potential of Nucleic Acid Therapeutics.

DNAzymes: Expanding the Potential of Nucleic Acid Therapeutics.

Nucleic acids drugs have been proven in the clinic as a powerful modality to treat inherited and acquired diseases. However, key challenges including drug stability, renal clearance, cellular uptake, and movement across biological barriers (foremost the blood-brain barrier) limit the translation and clinical efficacy of nucleic acid-based therapies, both systemically and in the central nervous system. In this study we provide an overview of an emerging class of nucleic acid therapeutic, called DNAzymes. In particular, we review the use of chemical modifications and carrier molecules for the stabilization and/or delivery of DNAzymes in cell and animal models. Although this review focuses on DNAzymes, the strategies described are broadly applicable to most nucleic acid technologies. This review should serve as a general guide for selecting chemical modifications to improve the therapeutic performance of DNAzymes.

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来源期刊
Nucleic acid therapeutics
Nucleic acid therapeutics BIOCHEMISTRY & MOLECULAR BIOLOGY-CHEMISTRY, MEDICINAL
CiteScore
7.60
自引率
7.50%
发文量
47
审稿时长
>12 weeks
期刊介绍: Nucleic Acid Therapeutics is the leading journal in its field focusing on cutting-edge basic research, therapeutic applications, and drug development using nucleic acids or related compounds to alter gene expression. The Journal examines many new approaches for using nucleic acids as therapeutic agents or in modifying nucleic acids for therapeutic purposes including: oligonucleotides, gene modification, aptamers, RNA nanoparticles, and ribozymes.
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