Development, Validation and Integration of in Silico Models to Identify Androgen Active Chemicals

Chemosphere. 2019 Apr;220:204-215. doi: 10.1016/j.chemosphere.2018.12.131. Epub 2018 Dec 19.

Abstract

Humans are exposed to large numbers of environmental chemicals, some of which potentially interfere with the endocrine system. The identification of potential endocrine disrupting chemicals (EDCs) has gained increasing priority in the assessment of environmental hazards. The U.S. Environmental Protection Agency (U.S. EPA) has developed the Endocrine Disruptor Screening Program (EDSP) which aims to prioritize and screen potential EDCs. The Toxicity Forecaster (ToxCast) program has generated data using in vitro high-throughput screening (HTS) assays measuring activity of chemicals at multiple points along the androgen receptor (AR) activity pathway. In the present study, using a large and diverse data set of 1667 chemicals provided by the U.S. EPA from the combined ToxCast AR assays in the framework of the Collaborative Modeling Project for Androgen Receptor Activity (CoMPARA). Two models were built using ADMET Predictor™; one is based on Artificial Neural Networks (ANNs) technology and the other uses a Support Vector Machine (SVM) algorithm; one model is a Decision Tree (DT) developed in R; and two models make use of differently combined sets of structural alerts (SAs) automatically extracted by SARpy. We used two strategies to integrate predictions from single models; one is based on a majority vote approach and the other on prediction convergence. These strategies led to enhanced statistical performance in most cases. Moreover, the majority vote approach improved prediction coverage when one or more single models were not able to provide any estimations. This study integrates multiple in silico approaches as a virtual screening tool for use in risk assessment of endocrine disrupting chemicals.

Keywords: Androgen receptor; Artificial neural networks; Decision tree; Endocrine disrupting chemicals; High-throughput screening; In silico; Support vector machine.

Publication types

  • Validation Study

MeSH terms

  • Algorithms*
  • Androgens / metabolism*
  • Computer Simulation
  • Endocrine Disruptors / analysis*
  • Endocrine Disruptors / metabolism
  • Endocrine Disruptors / toxicity
  • Endocrine System / drug effects*
  • High-Throughput Screening Assays / methods*
  • Humans
  • Models, Statistical*
  • Receptors, Androgen / metabolism*
  • United States
  • United States Environmental Protection Agency

Substances

  • Androgens
  • Endocrine Disruptors
  • Receptors, Androgen