基因组编辑
领域
疾病
遗传增强
知识库
计算机科学
工程伦理学
计算生物学
医学
清脆的
生物
遗传学
基因
万维网
病理
政治学
工程类
法学
作者
Fang Xu,Caiyan Zheng,Weihui Xu,Shiyao Zhang,Shanshan Liu,Xiaopeng Chen,Kai Yao
标识
DOI:10.3389/fphar.2024.1364135
摘要
The rapid evolution of gene editing technology has markedly improved the outlook for treating genetic diseases. Base editing, recognized as an exceptionally precise genetic modification tool, is emerging as a focus in the realm of genetic disease therapy. We provide a comprehensive overview of the fundamental principles and delivery methods of cytosine base editors (CBE), adenine base editors (ABE), and RNA base editors, with a particular focus on their applications and recent research advances in the treatment of genetic diseases. We have also explored the potential challenges faced by base editing technology in treatment, including aspects such as targeting specificity, safety, and efficacy, and have enumerated a series of possible solutions to propel the clinical translation of base editing technology. In conclusion, this article not only underscores the present state of base editing technology but also envisions its tremendous potential in the future, providing a novel perspective on the treatment of genetic diseases. It underscores the vast potential of base editing technology in the realm of genetic medicine, providing support for the progression of gene medicine and the development of innovative approaches to genetic disease therapy.
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