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RNA 靶向治疗药物。

RNA-Targeted Therapeutics.

机构信息

Ionis Pharmaceuticals, Inc., 2855 Gazelle Court, Carlsbad, CA 92010, USA.

University of California San Diego, 9500 Gilman Drive, La Jolla, CA 92093, USA.

出版信息

Cell Metab. 2018 Apr 3;27(4):714-739. doi: 10.1016/j.cmet.2018.03.004.

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.

摘要

RNA 靶向疗法代表了一种药物发现平台,涉及化学修饰的寡核苷酸、广泛的细胞 RNA 以及一种新型的靶标结合基序——沃森-克里克碱基配对。许多被许多人认为无法逾越的障碍已经被克服。如今,有四种 RNA 靶向疗法被批准用于商业用途,适应症包括脊髓性肌萎缩症(SMA)和降低低密度脂蛋白胆固醇(LDL-C),给药途径包括皮下、眼内和鞘内给药。该技术高效,并支持接近“不可成药”的靶标。另外三种药物正在注册过程中,还有更多的药物处于临床开发阶段,代表了多种化学和结构类别。此外,对这些药物作用机制的理解方面的进展,导致了临床疗效的稳步提高,以及可能用于治疗目的的广泛机制。在这里,我们总结了这个药物发现平台的进展、未来的挑战和机遇。

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