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An Adverse Outcome Pathway Network for Chemically Induced Oxidative Stress Leading to (Non)genotoxic Carcinogenesis
[Image: see text] Nongenotoxic (NGTX) carcinogens induce cancer via other mechanisms than direct DNA damage. A recognized mode of action for NGTX carcinogens is induction of oxidative stress, a state in which the amount of oxidants in a cell exceeds its antioxidant capacity, leading to regenerative...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10283045/ https://www.ncbi.nlm.nih.gov/pubmed/37156502 http://dx.doi.org/10.1021/acs.chemrestox.2c00396 |
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author | Veltman, Christina H. J. Pennings, Jeroen L. A. van de Water, Bob Luijten, Mirjam |
author_facet | Veltman, Christina H. J. Pennings, Jeroen L. A. van de Water, Bob Luijten, Mirjam |
author_sort | Veltman, Christina H. J. |
collection | PubMed |
description | [Image: see text] Nongenotoxic (NGTX) carcinogens induce cancer via other mechanisms than direct DNA damage. A recognized mode of action for NGTX carcinogens is induction of oxidative stress, a state in which the amount of oxidants in a cell exceeds its antioxidant capacity, leading to regenerative proliferation. Currently, carcinogenicity assessment of environmental chemicals primarily relies on genetic toxicity end points. Since NGTX carcinogens lack genotoxic potential, these chemicals may remain undetected in such evaluations. To enhance the predictivity of test strategies for carcinogenicity assessment, a shift toward mechanism-based approaches is required. Here, we present an adverse outcome pathway (AOP) network for chemically induced oxidative stress leading to (NGTX) carcinogenesis. To develop this AOP network, we first investigated the role of oxidative stress in the various cancer hallmarks. Next, possible mechanisms for chemical induction of oxidative stress and the biological effects of oxidative damage to macromolecules were considered. This resulted in an AOP network, of which associated uncertainties were explored. Ultimately, development of AOP networks relevant for carcinogenesis in humans will aid the transition to a mechanism-based, human relevant carcinogenicity assessment that involves a substantially lower number of laboratory animals. |
format | Online Article Text |
id | pubmed-10283045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-102830452023-06-22 An Adverse Outcome Pathway Network for Chemically Induced Oxidative Stress Leading to (Non)genotoxic Carcinogenesis Veltman, Christina H. J. Pennings, Jeroen L. A. van de Water, Bob Luijten, Mirjam Chem Res Toxicol [Image: see text] Nongenotoxic (NGTX) carcinogens induce cancer via other mechanisms than direct DNA damage. A recognized mode of action for NGTX carcinogens is induction of oxidative stress, a state in which the amount of oxidants in a cell exceeds its antioxidant capacity, leading to regenerative proliferation. Currently, carcinogenicity assessment of environmental chemicals primarily relies on genetic toxicity end points. Since NGTX carcinogens lack genotoxic potential, these chemicals may remain undetected in such evaluations. To enhance the predictivity of test strategies for carcinogenicity assessment, a shift toward mechanism-based approaches is required. Here, we present an adverse outcome pathway (AOP) network for chemically induced oxidative stress leading to (NGTX) carcinogenesis. To develop this AOP network, we first investigated the role of oxidative stress in the various cancer hallmarks. Next, possible mechanisms for chemical induction of oxidative stress and the biological effects of oxidative damage to macromolecules were considered. This resulted in an AOP network, of which associated uncertainties were explored. Ultimately, development of AOP networks relevant for carcinogenesis in humans will aid the transition to a mechanism-based, human relevant carcinogenicity assessment that involves a substantially lower number of laboratory animals. American Chemical Society 2023-05-08 /pmc/articles/PMC10283045/ /pubmed/37156502 http://dx.doi.org/10.1021/acs.chemrestox.2c00396 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Veltman, Christina H. J. Pennings, Jeroen L. A. van de Water, Bob Luijten, Mirjam An Adverse Outcome Pathway Network for Chemically Induced Oxidative Stress Leading to (Non)genotoxic Carcinogenesis |
title | An Adverse
Outcome Pathway Network for Chemically
Induced Oxidative Stress Leading to (Non)genotoxic Carcinogenesis |
title_full | An Adverse
Outcome Pathway Network for Chemically
Induced Oxidative Stress Leading to (Non)genotoxic Carcinogenesis |
title_fullStr | An Adverse
Outcome Pathway Network for Chemically
Induced Oxidative Stress Leading to (Non)genotoxic Carcinogenesis |
title_full_unstemmed | An Adverse
Outcome Pathway Network for Chemically
Induced Oxidative Stress Leading to (Non)genotoxic Carcinogenesis |
title_short | An Adverse
Outcome Pathway Network for Chemically
Induced Oxidative Stress Leading to (Non)genotoxic Carcinogenesis |
title_sort | adverse
outcome pathway network for chemically
induced oxidative stress leading to (non)genotoxic carcinogenesis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10283045/ https://www.ncbi.nlm.nih.gov/pubmed/37156502 http://dx.doi.org/10.1021/acs.chemrestox.2c00396 |
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