腺嘌呤碱基编辑作为一种有前途的治疗心血管疾病的方法

Lu-jia Yang, Zihao Tao, X. Ma, Xuanhui Zhang, Yuxuan Guo, Fei Gao
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摘要

心血管疾病(cvd)是全世界人类死亡的主要原因。遗传变异是心血管疾病的主要危险因素,在临床实践中治疗干预有限。最近基因组编辑技术的激增为纠正基因变异和治愈遗传疾病带来了希望。在众多基因组编辑工具中,腺嘌呤碱基编辑器(adenine base editors, abe)以高效率、高特异性、低脱靶效应等特点,成功进入临床试验,展现出改变现代心血管治疗的巨大潜力。在本文中,我们总结了ABE的基本知识,展示了在实验动物中使用ABE改善或治疗心血管疾病的三个标志性研究,最后讨论了未来应该解决的关键技术问题,以充分发挥ABE的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adenine base editing as a promising therapy for cardiovascular diseases
Cardiovascular diseases (CVDs) are the leading causes of human death worldwide. Genetic variants serve as the major risk factor for CVDs, with limited therapeutic interventions in clinical practice. The recent surge of genome editing technologies offers the hope to correct genetic variants and to cure genetic diseases. Among the diverse genome editing tools, adenine base editors (ABEs) exhibit high efficiency, high specificity, and low off-target effects, successfully entering a clinical trial and demonstrating the tremendous potential to transform modern cardiovascular therapy. In this review, we summarize the basic knowledge about ABE, showcase three hallmark studies using ABE to ameliorate or treat CVDs in experimental animals, and lastly discuss about the key technical concerns that should be addressed to achieve the full potential of ABEs in the future.
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