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Improved Identification of Human Hepatotoxic Potential by Summary Variables of Gene Expression.

ALTEX(2025)

Department of Statistics | German Federal Institute for Risk Assessment | Certara Simcyp Division

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Abstract
Prediction of hepatotoxicity in humans remains an unresolved challenge. Recently, an in-vitro/in-silico-method was established to predict blood concentrations of test compounds with an increased risk of causing human hepatotoxicity. In the present study, we addressed the question whether gene expression data can improve the quality of hepatotoxicity prediction compared to cytotoxicity analysis alone. A particular challenge is that high-dimensional gene expression data must be summarized into variables that allow for the determination of the lowest test compound concentration that causes altered gene expression. To address this challenge, we analyzed 60 hepatotoxic and non-hepatotoxic substances in a concentration dependent manner for cytotoxicity and expression of 3,524 probes, whose expression were previously reported to be influenced by hepatotoxicants. The toxicity separation index (TSI) was applied to quantify how well specific summary variables of gene expression are able to differentiate between the set of hepatotoxic and non-hepatotoxic substances. The best TSI was obtained when the lowest concentration of a test compound was considered positive that led to differential expression of two genes when compared to vehicle controls. Furthermore, the best gene expression-based summary variable was superior to cytotoxicity-based variables alone, and the combination of the best summary variables of gene expression and cytotoxicity data further improved the TSI compared to each category alone. In conclusion, the method used to derive summary variables of gene expression is critical and the best summary variables improve the prediction of hepatotoxic substances in relation to oral doses and blood concentrations in humans.
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要点】:本研究通过总结变量分析基因表达数据,提高了对人类肝毒性的预测质量,相较于单独的细胞毒性分析具有显著优势。

方法】:研究采用将高维基因表达数据汇总为可确定引起基因表达变化的最小测试化合物浓度的变量,并使用毒性分离指数(TSI)来评估这些变量的区分效果。

实验】:实验分析了60种肝毒性和非肝毒性物质在浓度依赖性下的细胞毒性和3,524个探针的表达,这些探针的表达先前报道受到肝毒物影响。实验结果显示,考虑测试化合物引起两个基因表达差异的最低浓度作为阳性标准时,得到的TSI最佳,且基因表达总结变量优于单独的细胞毒性变量,两者的结合进一步提高了TSI。