bioRxivBioinformaticsPreprint
Leveraging High-Throughput Screening Data and Conditional Generative Adversarial Networks to Advance Predictive Toxicology
Adrian J. GreeniD, Martin J. MohlenkampiD, Jhuma DasiD, Meenal ChaudhariiD, Lisa TruongiD, Robyn L. Tanguay, David M. ReifiD
Abstract
There are currently 85,000 chemicals registered with the Environmental Protection Agency (EPA) under the Toxic Substances Control Act, but only a small fraction have measured toxicological data. To address this gap, high-throughput screening (HTS) methods are vital. As part of one such HTS effort, embryonic zebrafish were used to examine a suite of morphological and mortality endpoints at six concentrations from over 1,000 unique chemicals found in the ToxCast library (phase 1 and 2). We hypothesized that by using a conditional Generative Adversarial Network (cGAN) and leveraging this large set of toxicity data, plus chemical structure information, we could efficiently predict toxic outcomes of untested chemicals. CAS numbers for each chemical were used to generate textual files containing three-dimensional structural information for each chemical. Utilizing a novel method in this space, we converted the 3D structural information into a weighted set of points while retaining all information about the structure. In vivo toxicity and chemical data were used to train two neural network generators. The first used regression (Go-ZT) while the second utilized cGAN architecture (GAN-ZT) to train a generator to produce toxicity data. Our results showed that both Go-ZT and GAN-ZT models produce similar results, but the cGAN achieved a higher sensitivity (SE) value of 85.7% vs 71.4%. Conversely, Go-ZT attained higher specificity (SP), positive predictive value (PPV), and Kappa results of 67.3%, 23.4%, and 0.21 compared to 24.5%, 14.0%, and 0.03 for the cGAN, respectively. By combining both Go-ZT and GAN-ZT, our consensus model improved the SP, PPV, and Kappa, to 75.5%, 25.0%, and 0.211, respectively, resulting in an area under the receiver operating characteristic (AUROC) of 0.663. Considering their potential use as prescreening tools, these models could provide in vivo toxicity predictions and insight into untested areas of the chemical space to prioritize compounds for HT testing. SummaryA conditional Generative Adversarial Network (cGAN) can leverage a large chemical set of experimental toxicity data plus chemical structure information to predict the toxicity of untested compounds.
- organism: zebrafish
- research focus: drug response / drug discovery
- approach: deep learning
- approach: statistical model
- Citations
- 1
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