A Systems Toxicology Approach for the Prediction of Kidney Toxicity and Its Mechanisms In Vitro. (15th January 2019)

• Record Type: Journal Article
• Authors: Ramm, Susanne; Todorov, Petar; Chandrasekaran, Vidya; Dohlman, Anders; Monteiro, Maria B; Pavkovic, Mira; Muhlich, Jeremy; Shankaran, Harish; Chen, William W; Mettetal, Jerome T; Vaidya, Vishal S
• Is Part Of: Toxicological sciences. Volume 169:Number 1(2019)
• Page Start: 54
• Page End: 69
• Publication Date: 2019-01-15
• Subjects: kidney toxicity -- prediction -- systems toxicology -- in vitro -- mechanism; Toxicology -- Periodicals; Toxicology -- Periodicals; Toxicology; Periodicals; 615.9
• DOI: 10.1093/toxsci/kfz021
• Languages: English
• ISSNs: 1096-6080

Abstract

Abstract: The failure to predict kidney toxicity of new chemical entities early in the development process before they reach humans remains a critical issue. Here, we used primary human kidney cells and applied a systems biology approach that combines multidimensional datasets and machine learning to identify biomarkers that not only predict nephrotoxic compounds but also provide hints toward their mechanism of toxicity. Gene expression and high-content imaging-derived phenotypical data from 46 diverse kidney toxicants were analyzed using Random Forest machine learning. Imaging features capturing changes in cell morphology and nucleus texture along with mRNA levels of HMOX1 and SQSTM1 were identified as the most powerful predictors of toxicity. These biomarkers were validated by their ability to accurately predict kidney toxicity of four out of six candidate therapeutics that exhibited toxicity only in late stage preclinical/clinical studies. Network analysis of similarities in toxic phenotypes was performed based on live-cell high-content image analysis at seven time points. Using compounds with known mechanism as reference, we could infer potential mechanisms of toxicity of candidate therapeutics. In summary, we report an approach to generate a multidimensional biomarker panel for mechanistic de-risking and prediction of kidney toxicity in in vitro for new therapeutic candidates and chemical entities.