清脆的
基因组编辑
计算生物学
生物
突变
染色体工程
基因组
遗传学
染色体易位
Cas9
基因组工程
生物信息学
突变
基因
作者
Clotilde Aussel,Toni Cathomen,Carla Fuster‐García
标识
DOI:10.1038/s41467-025-62606-z
摘要
CRISPR/Cas technology has revolutionized genome engineering, unlocking unprecedented therapeutic potential. However, beyond well-documented concerns of off-target (OT) mutagenesis, recent studies reveal a more pressing challenge: large structural variations (SVs), including chromosomal translocations and megabase-scale deletions, particularly in cells treated with DNA-PKcs inhibitors. These undervalued genomic alterations raise substantial safety concerns for clinical translation. As more CRISPR-based therapies progress toward the clinic, understanding and mitigating these risks is paramount. Here, we review emerging evidence on on-target aberrations and chromosomal translocations, identify key gaps in our understanding of the DNA repair pathways underlying these adverse effects, and discuss strategies to improve the safety of genome editing.
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