CardioDPi: An explainable deep-learning model for identifying cardiotoxic chemicals targeting hERG, Cav1.2, and Nav1.5 channels

J Hazard Mater. 2024 Aug 5:474:134724. doi: 10.1016/j.jhazmat.2024.134724. Epub 2024 May 24.

Abstract

The cardiotoxic effects of various pollutants have been a growing concern in environmental and material science. These effects encompass arrhythmias, myocardial injury, cardiac insufficiency, and pericardial inflammation. Compounds such as organic solvents and air pollutants disrupt the potassium, sodium, and calcium ion channels cardiac cell membranes, leading to the dysregulation of cardiac function. However, current cardiotoxicity models have disadvantages of incomplete data, ion channels, interpretability issues, and inability of toxic structure visualization. Herein, an interpretable deep-learning model known as CardioDPi was developed, which is capable of discriminating cardiotoxicity induced by the human Ether-à-go-go-related gene (hERG) channel, sodium channel (Na_v1.5), and calcium channel (Ca_v1.5) blockade. External validation yielded promising area under the ROC curve (AUC) values of 0.89, 0.89, and 0.94 for the hERG, Na_v1.5, and Ca_v1.5 channels, respectively. The CardioDPi can be freely accessed on the web server CardioDPipredictor (http://cardiodpi.sapredictor.cn/). Furthermore, the structural characteristics of cardiotoxic compounds were analyzed and structural alerts (SAs) can be extracted using the user-friendly CardioDPi-SAdetector web service (http://cardiosa.sapredictor.cn/). CardioDPi is a valuable tool for identifying cardiotoxic chemicals that are environmental and health risks. Moreover, the SA system provides essential insights for mode-of-action studies concerning cardiotoxic compounds.

Keywords: Cardiotoxicity; Environmental pollutants; Metal ion channels; Multilayer perceptron; Structural alerts.

MeSH terms

  • Calcium Channels, L-Type / chemistry
  • Calcium Channels, L-Type / drug effects
  • Calcium Channels, L-Type / metabolism
  • Cardiotoxicity / etiology
  • Cardiotoxins / chemistry
  • Cardiotoxins / toxicity
  • Deep Learning*
  • ERG1 Potassium Channel / antagonists & inhibitors
  • ERG1 Potassium Channel / metabolism
  • Humans
  • NAV1.5 Voltage-Gated Sodium Channel* / genetics
  • NAV1.5 Voltage-Gated Sodium Channel* / metabolism

Substances

  • NAV1.5 Voltage-Gated Sodium Channel
  • ERG1 Potassium Channel
  • Calcium Channels, L-Type
  • Cardiotoxins
  • SCN5A protein, human
  • KCNH2 protein, human