Division of Genetic and Molecular Toxicology, National Center for Toxicological Research, Jefferson, AR, USA.
J Environ Sci Health C Toxicol Carcinog. 2024;42(3):214-237. doi: 10.1080/26896583.2024.2331956. Epub 2024 Apr 2.
There has been growing interest in the use of human-derived metabolically competent cells for genotoxicity testing. The HepaRG cell line is considered one of the most promising cell models because it is TP53-proficient and retains many characteristics of primary human hepatocytes. In recent years, HepaRG cells, cultured in both a traditional two-dimensional (2D) format and as more advanced in-vivo-like 3D spheroids, have been employed in assays that measure different types of genetic toxicity endpoints, including DNA damage, mutations, and chromosomal damage. This review summarizes published studies that have used HepaRG cells for genotoxicity assessment, including cell model evaluation studies and risk assessment for various compounds. Both 2D and 3D HepaRG models can be adapted to several high-throughput genotoxicity assays, generating a large number of data points that facilitate quantitative benchmark concentration modeling. With further validation, HepaRG cells could serve as a unique, human-based new alternative methodology for genotoxicity testing.
人们对使用来源于人类的具有代谢能力的细胞进行遗传毒性测试越来越感兴趣。HepaRG 细胞系被认为是最有前途的细胞模型之一,因为它具有 TP53 功能,并且保留了许多原代人肝细胞的特征。近年来,HepaRG 细胞在传统的二维(2D)培养和更先进的类器官 3D 球体中被用于测量不同类型的遗传毒性终点的测定,包括 DNA 损伤、突变和染色体损伤。本综述总结了已使用 HepaRG 细胞进行遗传毒性评估的已发表研究,包括细胞模型评估研究和各种化合物的风险评估。二维和三维 HepaRG 模型都可以适应多种高通量遗传毒性测定,生成大量数据点,有利于定量基准浓度建模。经过进一步验证,HepaRG 细胞可以作为一种独特的、基于人类的遗传毒性测试新替代方法。