核酶
核糖核酸
小干扰RNA
适体
计算生物学
生物
RNA干扰
人类免疫缺陷病毒(HIV)
生物信息学
病毒学
遗传学
基因
作者
John Burnett,John J. Rossi
出处
期刊:Chemistry & Biology
[Elsevier BV]
日期:2012-01-01
卷期号:19 (1): 60-71
被引量:873
标识
DOI:10.1016/j.chembiol.2011.12.008
摘要
Recent advances of biological drugs have broadened the scope of therapeutic targets for a variety of human diseases. This holds true for dozens of RNA-based therapeutics currently under clinical investigation for diseases ranging from genetic disorders to HIV infection to various cancers. These emerging drugs, which include therapeutic ribozymes, aptamers, and small interfering RNAs (siRNAs), demonstrate the unprecedented versatility of RNA. However, RNA is inherently unstable, potentially immunogenic, and typically requires a delivery vehicle for efficient transport to the targeted cells. These issues have hindered the clinical progress of some RNA-based drugs and have contributed to mixed results in clinical testing. Nevertheless, promising results from recent clinical trials suggest that these barriers may be overcome with improved synthetic delivery carriers and chemical modifications of the RNA therapeutics. This review focuses on the clinical results of siRNA, RNA aptamer, and ribozyme therapeutics and the prospects for future successes.
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