An Adverse Outcome Pathway Network for Chemically Induced Oxidative Stress Leading to (Non)genotoxic Carcinogenesis.
Christina H J VeltmanJeroen L A PenningsBob van de WaterMirjam LuijtenPublished in: Chemical research in toxicology (2023)
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.
Keyphrases
- oxidative stress
- dna damage
- papillary thyroid
- ischemia reperfusion injury
- diabetic rats
- induced apoptosis
- squamous cell
- hydrogen peroxide
- endothelial cells
- signaling pathway
- network analysis
- gene expression
- young adults
- squamous cell carcinoma
- single cell
- dna methylation
- mesenchymal stem cells
- emergency department
- adverse drug
- mass spectrometry
- single molecule
- copy number
- endoplasmic reticulum stress
- lymph node metastasis
- induced pluripotent stem cells
- life cycle