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siRNA Versus miRNA as Therapeutics for Gene Silencing. | LitMetric

siRNA Versus miRNA as Therapeutics for Gene Silencing.

Mol Ther Nucleic Acids

Department of Pharmacology & Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong.

Published: September 2015

AI Article Synopsis

  • Small interfering RNAs (siRNAs) and microRNAs (miRNAs) are noncoding RNAs discovered over 20 years ago that play crucial roles in regulating genes and are being explored as potential treatments for various diseases, including cancer.
  • Both siRNAs and miRNAs are short RNA molecules that silence gene expression by targeting mRNA, but siRNAs are specific to a single target mRNA, while miRNAs can target multiple mRNAs, leading to different therapeutic strategies.
  • This review compares siRNAs and miRNAs regarding their mechanisms, properties, delivery methods, clinical uses, and the challenges faced in developing them as therapeutic agents.

Article Abstract

Discovered a little over two decades ago, small interfering RNAs (siRNAs) and microRNAs (miRNAs) are noncoding RNAs with important roles in gene regulation. They have recently been investigated as novel classes of therapeutic agents for the treatment of a wide range of disorders including cancers and infections. Clinical trials of siRNA- and miRNA-based drugs have already been initiated. siRNAs and miRNAs share many similarities, both are short duplex RNA molecules that exert gene silencing effects at the post-transcriptional level by targeting messenger RNA (mRNA), yet their mechanisms of action and clinical applications are distinct. The major difference between siRNAs and miRNAs is that the former are highly specific with only one mRNA target, whereas the latter have multiple targets. The therapeutic approaches of siRNAs and miRNAs are therefore very different. Hence, this review provides a comparison between therapeutic siRNAs and miRNAs in terms of their mechanisms of action, physicochemical properties, delivery, and clinical applications. Moreover, the challenges in developing both classes of RNA as therapeutics are also discussed.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4877448PMC
http://dx.doi.org/10.1038/mtna.2015.23DOI Listing

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