Benchmark Dose Analysis of DNA Damage Biomarker Responses Provides Compound Potency and Adverse Outcome Pathway Information for the Topoisomerase II Inhibitor Class of Compounds
| Autor: | Jeffrey C. Bemis, George E. Johnson, Derek T. Bernacki, Stephen D. Dertinger, Ryan P Wheeldon, Steven M. Bryce |
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| Rok vydání: | 2020 |
| Předmět: |
Epidemiology
DNA damage Health Toxicology and Mutagenesis Mutagen 010501 environmental sciences Biology Pharmacology medicine.disease_cause 01 natural sciences Cell Line 03 medical and health sciences Adverse Outcome Pathway medicine Humans Topoisomerase II Inhibitors Potency Mode of action Genetics (clinical) 030304 developmental biology 0105 earth and related environmental sciences 0303 health sciences Adverse Outcome Pathways Mutagenicity Tests Topoisomerase Cell Cycle biology.protein Topoisomerase-II Inhibitor Genotoxicity DNA Damage Mutagens |
| Zdroj: | Environmental and Molecular Mutagenesis. 61:396-407 |
| ISSN: | 1098-2280 0893-6692 |
| DOI: | 10.1002/em.22360 |
| Popis: | Genetic toxicology data have traditionally been utilized for hazard identification to provide a binary call for a compound's risk. Recent advances in the scientific field, especially with the development of high-throughput methods to quantify DNA damage, have influenced a change of approach in genotoxicity assessment. The in vitro MultiFlow® DNA Damage Assay is one such method which multiplexes γH2AX, p53, phospho-histone H3 biomarkers into a single-flow cytometric analysis (Bryce et al., [2016]: Environ Mol Mutagen 57:546-558). This assay was used to study human TK6 cells exposed to each of eight topoisomerase II poisons for 4 and 24 hr. Using PROAST v65.5, the Benchmark Dose approach was applied to the resulting flow cytometric datasets. With "compound" serving as covariate, all eight compounds were combined into a single analysis, per time point and endpoint. The resulting 90% confidence intervals, plotted in Log scale, were considered as the potency rank for the eight compounds. The in vitro MultiFlow data showed a maximum confidence interval span of 1Log, which indicates data of good quality. Patterns observed in the compound potency rank were scrutinized by using the expert rule-based software program Derek Nexus, developed by Lhasa Limited. Compound sub-classification and structural alerts were considered contributory to the potencies observed for the topoisomerase II poisons studied herein. The Topo II poison Adverse Outcome Pathway was evaluated with MultiFlow endpoints serving as Key Events. The step-wise approach described herein can be considered as a foundation for risk assessment of compounds within a specific mode of action of interest. Environ. Mol. Mutagen. 2020. © 2020 Wiley Periodicals, Inc. |
| Databáze: | OpenAIRE |
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