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Prediction of Non-genotoxic Hepatocarcinogenicity Using Chemical-Protein Interactions

机译:使用化学蛋白质相互作用预测非遗传毒性肝癌发生性

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The assessment of non-genotoxic hepatocarcinogenicity of chemicals is currently based on 2-year rodent bioassays. It is desirable to develop a fast and effective method to accelerate the identification of potential hepatocarcinogenicity of non-genotoxic chemicals. In this study, a novel method CPI is proposed to predict potential hepatocarcinogenicity of non-genotoxic chemicals. The CPI method is based on chemical-protein interactions and interpretable decision tree classifiers. The interpretable rules generated by the CPI method are analyzed to provide insights into the mechanism and biomarkers of non-genotoxic hepatocarcinogenicity. The CPI method with an independent test accuracy of 86% using only 1 protein biomarker outperforms the state-of-the-art methods of gene expression profile-based toxicogenomics using 90 gene biomarkers. A protein ABCC3 was identified as a potential protein biomarker for further exploration. This study presents the potential application of CPI method for assessing non-genotoxic hepatocarcinogenicity of chemicals.
机译:目前基于2年的啮齿动物生物测定的化学品的非基因毒性肝癌的评估。期望开发一种快速有效的方法,以加速非遗传毒性化学品的潜在肝癌性的方法。在该研究中,提出了一种新的方法CPI,以预测非遗传毒性化学品的潜在肝癌性。 CPI方法基于化学蛋白质相互作用和可解释的决策树分类器。分析了CPI方法产生的可解释规则,以提供对非基因毒性肝癌的机制和生物标志物的见解。使用仅使用90个基因生物标志物的基因表达谱的基因表达毒源组学的独立测试精度为86%的CPI方法。蛋白ABCC3被鉴定为潜在的蛋白质生物标志物,以进一步探索。本研究介绍了CPI方法评估化学品的非基因毒性肝癌的潜在应用。

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