RNA干扰
小干扰RNA
基因沉默
计算生物学
反式siRNA
生物
核糖核酸
基因
遗传学
作者
Tiejun Li,Meihua Wu,York Yuanyuan Zhu,Jian‐Xin Chen,Li Chen
出处
期刊:Nucleic Acid Therapeutics
[Mary Ann Liebert]
日期:2014-08-01
卷期号:24 (4): 302-312
被引量:23
标识
DOI:10.1089/nat.2014.0480
摘要
RNA interference (RNAi) has been proven in recent years to be a newly advanced and powerful tool for development of therapeutic agents toward various unmet medical needs such as cancer, in particular, a great attention has been paid to the development of antineoplastic agents. Recent success in clinical trials related to RNAi-based therapeutics on cancer and ocular disease has validated that small interfering RNAs (siRNAs) constitute a new promising class of therapeutics. Currently, a great wealth of multi-target based siRNA structural modifications is available for promoting siRNA-mediated gene silencing with low side effects. Here, the latest developments in RNAi-based therapeutics and novel structural modifications described for siRNAs—in particular multi-target siRNAs—are reviewed.
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