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Predictability of drug-induced liver injury by machine learning

机译:机器学习药物诱导肝损伤的可预测性

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Drug-induced liver injury (DILI) is a major concern in drug development, as hepatotoxicity may not be apparent at early stages but can lead to life threatening consequences. The ability to predict DILI from in vitro data would be a crucial advantage. In 2018, the Critical Assessment Massive Data Analysis group proposed the CMap Drug Safety challenge focusing on DILI prediction. The challenge data included Affymetrix GeneChip expression profiles for the two cancer cell lines MCF7 and PC3 treated with 276 drug compounds and empty vehicles. Binary DILI labeling and a recommended train/test split for the development of predictive classification approaches were also provided. We devised three deep learning architectures for DILI prediction on the challenge data and compared them to random forest and multi-layer perceptron classifiers. On a subset of the data and for some of the models we additionally tested several strategies for balancing the two DILI classes and to identify alternative informative train/test splits. All the models were trained with the MAQC data analysis protocol (DAP), i.e., 10x5 cross-validation over the training set. In all the experiments, the classification performance in both cross-validation and external validation gave Matthews correlation coefficient (MCC) values below 0.2. We observed minimal differences between the two cell lines. Notably, deep learning approaches did not give an advantage on the classification performance. We extensively tested multiple machine learning approaches for the DILI classification task obtaining poor to mediocre performance. The results suggest that the CMap expression data on the two cell lines MCF7 and PC3 are not sufficient for accurate DILI label prediction. This article was reviewed by Maciej Kandula and Pawe? P. Labaj.
机译:药物诱导的肝损伤(Dili)是药物开发的主要关注点,因为肝毒性在早期阶段可能不明显,但会导致危及生命的后果。从体外数据预测DILI的能力将是至关重要的优势。 2018年,批判性评估大规模数据分析集团提出了重点关注帝力预测的CMAP药物安全挑战。挑战数据包括两种癌细胞系MCF7和PC3的Affymetrix GeneChip表达曲线,用276种药物化合物和空载体处理。还提供了二环帝国标签和推荐的火车/测试分裂,用于开发预测分类方法。我们为挑战数据进行了三个深入的学习架构,并将其与随机森林和多层的Perceptron分类器进行了比较。在数据的子集和某些型号的子集上,我们另外测试了若干策略,用于平衡两个DILI类,并识别替代的信息列车/测试分裂。所有模型都培训了MAQC数据分析协议(DAP),即通过训练集的10x5交叉验证。在所有实验中,交叉验证和外部验证中的分类性能使Matthews相关系数(MCC)值低于0.2。我们观察到两种细胞系之间的最小差异。值得注意的是,深入学习方法并未对分类性能产生优势。我们广泛测试了帝力分类任务的多机器学习方法,从而获得差的平庸性能。结果表明,两个单元线MCF7和PC3上的CMAP表达数据不足以准确的帝力标签预测。本文由Maciej Kandula和Pawe审核? P. Labaj。

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