Aussel Clotilde, Cathomen Toni, Fuster-García Carla
Institute for Transfusion Medicine and Gene Therapy, Medical Center - University of Freiburg, Freiburg, Germany.
Center for Cell and Gene Therapy Freiburg (CGF), Medical Center - University of Freiburg, Freiburg, Germany.
Nat Commun. 2025 Aug 5;16(1):7208. doi: 10.1038/s41467-025-62606-z.
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.
CRISPR/Cas技术彻底改变了基因组工程,释放出了前所未有的治疗潜力。然而,除了有充分记录的脱靶(OT)诱变问题外,最近的研究揭示了一个更为紧迫的挑战:大规模结构变异(SVs),包括染色体易位和兆碱基规模的缺失,尤其是在用DNA-PKcs抑制剂处理的细胞中。这些被低估的基因组改变给临床转化带来了重大的安全问题。随着越来越多基于CRISPR的疗法进入临床阶段,了解并减轻这些风险至关重要。在此,我们综述了关于靶向异常和染色体易位的新证据,确定了我们对这些不良反应背后的DNA修复途径理解上的关键空白,并讨论了提高基因组编辑安全性的策略。