3.8 Article

In silico approaches in organ toxicity hazard assessment: Current status and future needs for predicting heart, kidney and lung toxicities

Journal

COMPUTATIONAL TOXICOLOGY
Volume 20, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.comtox.2021.100188

Keywords

In Silico; Computational toxicology; Organ toxicity; In Silico toxicology protocols; Kidney; Heart; Lung; Hazard identification; Risk assessment; QSAR; Expert alerts; Read-across

Categories

Funding

  1. National Institute of Environmental Health Sciences of the National Institutes of Health [R44ES026909]

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Current methodologies are being developed to predict kidney, heart, and lung toxicities based on in vitro and in silico approaches, but face obstacles such as a lack of comprehensive mechanistic understanding, limited in vitro testing approaches, and limited in vivo databases suitable for modeling.
The kidneys, heart and lungs are vital organ systems evaluated as part of acute or chronic toxicity assessments. New methodologies are being developed to predict these adverse effects based on in vitro and in silico approaches. This paper reviews the current state of the art in predicting these organ toxicities. It outlines the biological basis, processes and endpoints for kidney toxicity, pulmonary toxicity, respiratory irritation and sensitization as well as functional and structural cardiac toxicities. The review also covers current experimental approaches, including off-target panels from secondary pharmacology batteries. Current in silico approaches for prediction of these effects and mechanisms are described as well as obstacles to the use of in silico methods. Ultimately, a commonly accepted protocol for performing such assessment would be a valuable resource to expand the use of such approaches across different regulatory and industrial applications. However, a number of factors impede their widespread deployment including a lack of a comprehensive mechanistic understanding, limited in vitro testing approaches and limited in vivo databases suitable for modeling, a limited understanding of how to incorporate absorption, distribution, metabolism, and excretion (ADME) considerations into the overall process, a lack of in silico models designed to predict a safe dose and an accepted framework for organizing the key characteristics of these organ toxicants.

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