Abstract

The ability to computationally predict the effects of toxic compounds on humans could help address the deficiencies of current chemical safety testing. Here, we report the results from a community-based DREAM challenge to predict toxicities of environmental compounds with potential adverse health effects for human populations. We measured the cytotoxicity of 156 compounds in 884 lymphoblastoid cell lines for which genotype and transcriptional data are available as part of the Tox21 1000 Genomes Project. The challenge participants developed algorithms to predict interindividual variability of toxic response from genomic profiles and population-level cytotoxicity data from structural attributes of the compounds. 179 submitted predictions were evaluated against an experimental data set to which participants were blinded. Individual cytotoxicity predictions were better than random, with modest correlations (Pearson's r < 0.28), consistent with complex trait genomic prediction. In contrast, predictions of population-level response to different compounds were higher (r < 0.66). The results highlight the possibility of predicting health risks associated with unknown compounds, although risk estimation accuracy remains suboptimal.

Original languageEnglish
Pages (from-to)933-940
Number of pages8
JournalNature Biotechnology
Volume33
Issue number9
DOIs
Publication statusPublished - 10 Sept 2015
MoE publication typeA1 Journal article-refereed

Funding

This research was supported in part by the US National Institutes of Health (NIH), National Institute of Environmental Health Sciences (NIEHS). This work was made possible by US Environmental Protection Agency grants STAR RD83516601 and RD83382501, NIH grants R01CA161608 and R01HG006292, and through an interagency agreement (IAG #Y2-ES-7020-01) from NIEHS to NCATS. F.E. thanks European Molecular Biology Laboratory Interdisciplinary Post-Docs (EMBL EIPOD) and Marie Curie Actions (COFUND) for funding. Best performing team was funded by NIH grants 5R01CA152301 and 1R01CA172211.

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