Center for Genetic Diseases, Chicago Medical School, Rosalind Franklin University of Medicine and Science, North Chicago, IL, USA.
Methods Mol Biol. 2022;2537:21-36. doi: 10.1007/978-1-0716-2521-7_2.
Targeting of pre-mRNA splicing has yielded a rich variety of strategies for altering gene expression as a treatment for disease. The search for therapeutics that can modulate splicing has been dominated by antisense oligonucleotides (ASOs) and small molecule compounds, with each platform achieving remarkably effective results in the clinic. The success of RNA-targeting drugs has led to the exploration of new strategies to expand the repertoire of this type of therapeutic. Here, we discuss some of the more common causes of faulty gene expression and provide examples of approaches that have been developed to target and correct these defects for therapeutic value.
靶向前体 mRNA 剪接为改变疾病治疗中的基因表达提供了丰富多样的策略。寻找能够调节剪接的治疗方法一直以反义寡核苷酸 (ASO) 和小分子化合物为主导,每种平台在临床上都取得了非常有效的结果。RNA 靶向药物的成功导致了探索新策略来扩展这种治疗类型的治疗 repertoire 的探索。在这里,我们讨论了一些常见的导致基因表达错误的原因,并提供了一些针对这些缺陷进行靶向和纠正的方法示例,以实现治疗价值。