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A novel genotoxin-specific qPCR array based on the metabolically competent human HepaRG (TM) cell line as a rapid and reliable tool for improved in vitro hazard assessment

机译:一种基于代谢态有患者肝脏(TM)细胞系的新型基因毒素特异性QPCR阵列作为一种快速可靠的工具,可改善体外危害评估

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摘要

Although the value of the regulatory accepted batteries for in vitro genotoxicity testing is recognized, they result in a high number of false positives. This has a major impact on society and industries developing novel compounds for pharmaceutical, chemical, and consumer products, as afflicted compounds have to be (prematurely) abandoned or further tested on animals. Using the metabolically competent human HepaRG (TM) cell line and toxicogenomics approaches, we have developed an upgraded, innovative, and proprietary gene classifier. This gene classifier is based on transcriptomic changes induced by 12 genotoxic and 12 non-genotoxic reference compounds tested at sub-cytotoxic concentrations, i.e., IC10 concentrations as determined by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. The resulting gene classifier was translated into an easy-to-handle qPCR array that, as shown by pathway analysis, covers several different cellular processes related to genotoxicity. To further assess the predictivity of the tool, a set of 5 known positive and 5 known negative test compounds for genotoxicity was evaluated. In addition, 2 compounds with debatable genotoxicity data were tested to explore how the qPCR array would classify these. With an accuracy of 100%, when equivocal results were considered positive, the results showed that combining HepaRG (TM) cells with a genotoxin-specific qPCR array can improve (geno)toxicological hazard assessment. In addition, the developed qPCR array was able to provide additional information on compounds for which so far debatable genotoxicity data are available. The results indicate that the new in vitro tool can improve human safety assessment of chemicals in general by basing predictions on mechanistic toxicogenomics information.
机译:虽然认识到用于体外遗传毒性测试的监管所接受的电池的价值,但它们导致误报率大。这对社会和行业产生了重大影响,该社会和行业为制药,化学品和消费产品开发了新型化合物,因为患有患病的化合物必须(过早)被遗弃或进一步测试动物。使用代谢态有态性的人类肝细胞系和毒源组合方法,我们开发了升级,创新和专有的基因分类器。该基因分类器基于12个基因毒性和12个非遗传毒性参考化合物在亚细胞毒性浓度下测试的转录组变化,即IC10浓度,如3-(4,5-二甲基噻唑-2-基)-2, 5-二苯基四唑鎓溴(MTT)测定。将得到的基因分类器转化为易于处理的QPCR阵列,如通过途径分析所示,涵盖与遗传毒性有关的几种不同的细胞过程。为了进一步评估工具的预测性,评价了一组已知的阳性和5个已知的用于基因毒性的负测试化合物。此外,测试了2种具有易毒性遗传毒性数据的化合物,以探索QPCR阵列如何对这些进行分类。当准确性为100%时,当阳性结果被认为是阳性时,结果表明,将Heparg(TM)细胞与遗传毒素特异性QPCR阵列组合可以改善(Geno)毒理学危害评估。此外,发达的QPCR阵列能够提供有关该化合物的额外信息,因此可获得的可易脱毒性毒性数据。结果表明,新的体外工具通过基于机械毒物学信息的预测来改善化学品的人性安全评估。

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