解锁CRISPR-Cas9治疗囊性纤维化的潜力:详细综述

IF 2.6 3区 生物学 Q2 GENETICS & HEREDITY Gene Pub Date : 2025-03-20 Epub Date: 2025-01-18 DOI:10.1016/j.gene.2025.149257
Hudson Harris, Javeed Kittur
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引用次数: 0

摘要

CRISPR-Cas9技术彻底改变了基因工程,提供了精确高效的基因组编辑能力。本文综述了CRISPR-Cas9在囊性纤维化(CF)中的应用,特别是针对CFTR基因突变。CF是一种多器官疾病,主要影响肺部、胃肠系统(如CF相关糖尿病(CFRD)、CF相关肝病(CFLD))、骨骼(CF-bone disease)和生殖系统。CF是一种以离子转运缺陷导致粘稠粘液积聚为特征的遗传性疾病,通常由CFTR基因ΔF508等突变引起。本综述采用系统的方法,结合多个学术数据库(包括PubMed、Web of Science和ScienceDirect)的广泛文献检索,确定了40项高质量的研究,重点关注CRISPR-Cas9在CFTR基因编辑中的应用。数据收集过程涉及针对实验方法、基因编辑结果、传递方法和验证技术的预定义纳入标准。数据分析综合了编辑效率、脱靶效应和传递系统优化方面的发现,对该领域进行了全面的概述。这篇综述重点介绍了CRISPR-Cas9的历史发展、其机制及其在基因工程和医学中的变革作用。对CRISPR-Cas9在CFTR基因校正中的应用的详细研究强调了治疗干预的潜力,同时解决了脱靶效应、传递效率和伦理考虑等挑战。未来的方向包括优化输送系统,整合高级编辑工具,如主要和基础编辑,以及扩展个性化医疗方法以改善治疗结果。通过系统分析目前的情况,本综述为推进CRISPR-Cas9技术治疗囊性纤维化及相关疾病提供了基础。
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Unlocking the potential of CRISPR-Cas9 for cystic fibrosis: A systematic literature review.

CRISPR-Cas9 technology has revolutionized genetic engineering, offering precise and efficient genome editing capabilities. This review explores the application of CRISPR-Cas9 for cystic fibrosis (CF), particularly targeting mutations in the CFTR gene. CF is a multiorgan disease primarily affecting the lungs, gastrointestinal system (e.g., CF-related diabetes (CFRD), CF-associated liver disease (CFLD)), bones (CF-bone disease), and the reproductive system. CF, a genetic disorder characterized by defective ion transport leading to thick mucus accumulation, is often caused by mutations like ΔF508 in the CFTR gene. This review employs a systematic methodology, incorporating an extensive literature search across multiple academic databases, including PubMed, Web of Science, and ScienceDirect, to identify 40 high-quality studies focused on CRISPR-Cas9 applications for CFTR gene editing. The data collection process involved predefined inclusion criteria targeting experimental approaches, gene-editing outcomes, delivery methods, and verification techniques. Data analysis synthesized findings on editing efficiency, off-target effects, and delivery system optimization to present a comprehensive overview of the field. The review highlights the historical development of CRISPR-Cas9, its mechanism, and its transformative role in genetic engineering and medicine. A detailed examination of CRISPR-Cas9's application in CFTR gene correction emphasizes the potential for therapeutic interventions while addressing challenges such as off-target effects, delivery efficiency, and ethical considerations. Future directions include optimizing delivery systems, integrating advanced editing tools like prime and base editing, and expanding personalized medicine approaches to improve treatment outcomes. By systematically analyzing the current landscape, this review provides a foundation for advancing CRISPR-Cas9 technologies for cystic fibrosis treatment and related disorders.

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来源期刊
Gene
Gene 生物-遗传学
CiteScore
6.10
自引率
2.90%
发文量
718
审稿时长
42 days
期刊介绍: Gene publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses.
期刊最新文献
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