Toxys B.V., 2333 CG Leiden, The Netherlands.
Toxicol Sci. 2020 Sep 1;177(1):202-213. doi: 10.1093/toxsci/kfaa103.
Understanding the mode-of-action (MOA) of genotoxic compounds and differentiating between direct DNA interaction and indirect genotoxicity is crucial for their reliable safety assessment. ToxTracker is a stem cell-based reporter assay that detects activation of various cellular responses that are associated with genotoxicity and cancer. ToxTracker consists of 6 different GFP reporter cell lines that can detect the induction of DNA damage, oxidative stress, and protein damage in a single test. The assay can thereby provide insight into the MOA of compounds. Genotoxicity is detected in ToxTracker by activation of 2 independent GFP reporters. Activation of the Bscl2-GFP reporter is associated with induction of DNA adducts and subsequent inhibition of DNA replication and the Rtkn-GFP reporter is activated following the formation of DNA double-strand breaks. Here, we show that the differential activation of these 2 genotoxicity reporters could be used to further differentiate between a DNA reactive and clastogenic or a non-DNA-reactive aneugenic MOA of genotoxic compounds. For further classification of aneugenic and clastogenic compounds, the ToxTracker assay was extended with cell cycle analysis and aneuploidy assessment. The extension was validated using a selection of 16 (genotoxic) compounds with a well-established MOA. Furthermore, indirect genotoxicity related to the production of reactive oxygen species was investigated using the DNA damage and oxidative stress ToxTracker reporters in combination with different reactive oxygen species scavengers. With these new extensions, ToxTracker was able to accurately classify compounds as genotoxic or nongenotoxic and could discriminate between DNA-reactive compounds, aneugens, and indirect genotoxicity caused by oxidative stress.
了解遗传毒性化合物的作用模式(MOA)并区分直接 DNA 相互作用和间接遗传毒性对于其可靠的安全性评估至关重要。ToxTracker 是一种基于干细胞的报告基因检测试剂盒,可检测与遗传毒性和癌症相关的各种细胞反应的激活。ToxTracker 由 6 种不同的 GFP 报告细胞系组成,可以在单次检测中检测 DNA 损伤、氧化应激和蛋白质损伤的诱导。该检测试剂盒可提供有关化合物 MOA 的信息。ToxTracker 中的遗传毒性通过 2 个独立的 GFP 报告基因的激活来检测。Bscl2-GFP 报告基因的激活与 DNA 加合物的诱导及其随后的 DNA 复制抑制有关,而 Rtkn-GFP 报告基因则在 DNA 双链断裂形成后被激活。在这里,我们表明,这 2 个遗传毒性报告基因的差异激活可用于进一步区分遗传毒性化合物的 DNA 反应性和断裂剂或非 DNA 反应性的致整倍性作用模式。为了进一步对致整倍体和断裂剂化合物进行分类,ToxTracker 检测试剂盒通过细胞周期分析和非整倍体评估进行了扩展。该扩展使用一组具有明确 MOA 的 16 种(遗传毒性)化合物进行了验证。此外,还使用 DNA 损伤和氧化应激 ToxTracker 报告基因与不同的活性氧清除剂组合,研究了与活性氧产生相关的间接遗传毒性。通过这些新的扩展,ToxTracker 能够准确地将化合物分类为遗传毒性或非遗传毒性,并能够区分 DNA 反应性化合物、致整倍体和由氧化应激引起的间接遗传毒性。