Bohne Jens, Cathomen Toni
Hannover Medical School, Department of Virology, OE 5230, Carl-Neuberg-Str 1, D-30625 Hannover, Germany.
Curr Opin Mol Ther. 2008 Jun;10(3):214-23.
Genotoxicity is a collective term that includes any process which affects the integrity of genomic DNA. With regard to gene therapy, the insertion of genetic elements and the expression of DNA-modifying proteins are the main mediators of genotoxic side effects. The practicability of gene-addition-type gene therapy protocols has been demonstrated in several successful clinical trials, but the risk of insertional mutagenesis remains a major obstacle. Targeted strategies aimed at correcting a mutation directly in the genome can preserve temporal and tissue-specific expression of the afflicted gene. However, sufficient gene targeting frequency can only be achieved upon expression of tailor-made nucleases. Partly because of insufficient specificity, such designer nucleases can challenge genome integrity. Here, the origin and the consequences of genotoxicity are reviewed, with a focus on assays that have been developed to assess genotoxicity. In addition, approaches to reduce toxicity associated with the major gene therapy strategies are discussed.
基因毒性是一个统称,包括任何影响基因组DNA完整性的过程。就基因治疗而言,遗传元件的插入和DNA修饰蛋白的表达是基因毒性副作用的主要介导因素。基因添加型基因治疗方案的实用性已在多项成功的临床试验中得到证明,但插入诱变的风险仍然是一个主要障碍。旨在直接纠正基因组中突变的靶向策略可以保留患病基因的时间和组织特异性表达。然而,只有在表达定制核酸酶后才能实现足够的基因靶向频率。部分由于特异性不足,这种设计核酸酶可能会挑战基因组完整性。在此,对基因毒性的起源和后果进行综述,重点关注已开发用于评估基因毒性的检测方法。此外,还讨论了降低与主要基因治疗策略相关毒性的方法。