| Literature DB >> 29617640 |
Stanley T Crooke1, Joseph L Witztum2, C Frank Bennett3, Brenda F Baker3.
Abstract
RNA-targeted therapies represent a platform for drug discovery involving chemically modified oligonucleotides, a wide range of cellular RNAs, and a novel target-binding motif, Watson-Crick base pairing. Numerous hurdles considered by many to be impassable have been overcome. Today, four RNA-targeted therapies are approved for commercial use for indications as diverse as Spinal Muscular Atrophy (SMA) and reduction of low-density lipoprotein cholesterol (LDL-C) and by routes of administration including subcutaneous, intravitreal, and intrathecal delivery. The technology is efficient and supports approaching "undruggable" targets. Three additional agents are progressing through registration, and more are in clinical development, representing several chemical and structural classes. Moreover, progress in understanding the molecular mechanisms by which these drugs work has led to steadily better clinical performance and a wide range of mechanisms that may be exploited for therapeutic purposes. Here we summarize the progress, future challenges, and opportunities for this drug discovery platform.Entities:
Keywords: GalNAc; RNAi; anti-miRs; antisense; oligonucleotide; siRNA
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Year: 2018 PMID: 29617640 DOI: 10.1016/j.cmet.2018.03.004
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287