RNA编辑
阿达尔
核糖核酸
计算生物学
基因组编辑
腺苷脱氨酶
清脆的
小RNA
生物
计算机科学
人类疾病
生物信息学
引导RNA
腺苷
RNA沉默
RNA剪接
Cas9
小发夹RNA
核酶
非编码RNA
遗传学
钥匙(锁)
作者
Jinsil Kim,Hyuk Gyoon Lee,Minwook Shin
出处
期刊:Nucleic Acid Therapeutics
[Mary Ann Liebert, Inc.]
日期:2026-04-01
卷期号:36 (2): 61-83
标识
DOI:10.1177/21593337251415115
摘要
Adenosine deaminase acting on RNA (ADAR)-mediated RNA editing has emerged as a powerful and precise technology for modifying RNA transcripts, enabling correction of disease-causing mutations without permanent changes to the genome. Recent advances in ADAR protein engineering, guide RNA design, and delivery methods have significantly improved editing efficiency and specificity, overcoming many initial limitations. These developments have expanded the therapeutic potential of ADAR-based editing across a range of conditions, including genetic disorders, cancer, metabolic diseases, and neurodegenerative disorders. Notably, several ADAR-based therapeutics have now entered early clinical trials, marking a critical milestone in translating this technology from bench to bedside. Moreover, its inherent programmability, reversibility, and transient nature make ADAR-mediated RNA editing a highly attractive platform for personalized medicine, enabling tailored interventions based on individual genetic profiles and disease contexts. This review provides a comprehensive comparison of recent innovative advancements in ADAR-based RNA editing technologies, their use in diverse contexts pertinent to human diseases, the key challenges that remain, and future directions for their therapeutic implementation.
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