Contemporary Progress and Opportunities in RNA-Targeted Drug Discovery

被引:19
|
作者
Garner, Amanda L. [1 ]
机构
[1] Univ Michigan, Coll Pharm, Dept Med Chem, Ann Arbor, MI 48109 USA
来源
ACS MEDICINAL CHEMISTRY LETTERS | 2023年 / 14卷 / 03期
基金
美国国家卫生研究院;
关键词
RNAs; RNA structure; RNA-targeted drug discovery; small molecules; SMALL-MOLECULE INHIBITION; BINDING SMALL MOLECULES; TAR RNA; INTERNAL LOOPS; RIBOSOMAL-RNA; DISPLACEMENT ASSAY; SPLICING MODIFIER; HOECHST; 33258; DESIGN; SELECTION;
D O I
10.1021/acsmedchemlett.3c00020
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The surprising discovery that RNAs are the predominant gene products to emerge from the human genome catalyzed a renaissance in RNA biology. It is now well-understood that RNAs act as more than just a messenger and comprise a large and diverse family of ribonucleic acids of differing sizes, structures, and functions. RNAs play expansive roles in the cell, contributing to the regulation and fine-tuning of nearly all aspects of gene expression and genome architecture. In line with the significance of these functions, we have witnessed an explosion in discoveries connecting RNAs with a variety of human diseases. Consequently, the targeting of RNAs, and more broadly RNA biology, has emerged as an untapped area of drug discovery, making the search for RNA-targeted therapeutics of great interest. In this Microperspective, I highlight contemporary learnings in the field and present my views on how to catapult us toward the systematic discovery of RNA-targeted medicines.
引用
收藏
页码:251 / 259
页数:9
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