1. A tiered approach to investigate the inhalation toxicity of cobalt substances. Tier 2 b: Reactive cobalt substances induce oxidative stress in ToxTracker and activate hypoxia target genes.
- Author
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Derr R, Moelijker N, Hendriks G, and Brandsma I
- Subjects
- Administration, Inhalation, Cell Line, Cell Survival drug effects, Dose-Response Relationship, Drug, Genotype, Mutagenicity Tests, Oxidoreductases Acting on Sulfur Group Donors genetics, Particle Size, Carcinogens chemistry, Carcinogens pharmacology, Cobalt chemistry, Cobalt pharmacology, Oxidative Stress drug effects, Oxidative Stress genetics
- Abstract
Cobalt metal and cobalt sulfate are carcinogenic in rodents following inhalation exposure. The pre-carcinogenic effects associated with exposure to these cobalt substances include oxidative stress and genotoxicity. Some, but not all, cobalt substances induce in vitro clastogenicity or an increase in micronuclei. As a result, these substances are classified genotoxic carcinogens, having major impacts on their risk assessment, e.g. assumption of a non-thresholded dose response. Here, we investigated the potential of nine cobalt substances to cause genotoxicity and oxidative stress using the ToxTracker assay, with an extension to measure biomarkers of hypoxia. None of the nine tested substances activated the DNA damage markers in ToxTracker, and five substances activated the oxidative stress response reporters. The same five substances also activated the expression of several hypoxia target genes. Consistent with the lower tier of testing found in the preceding paper of this series, these compounds can be grouped based on their ability to release bioavailable cobalt ion and to trigger subsequent key events., (Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.)
- Published
- 2022
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