Portal:AOP/Mission
From WikiPathways
The purpose of this portal is to create a collection of AOPs on the molecular level for the AOPs that are, or will be created for the EU-ToxRisk program, in which Open PHACTS Foundation (OPF) is responsible for AOP creation. The subjects of the first AOPs are linked to the use cases of the EU-ToxRisk program, and there will be a team of experts involved in the creation of each AOP.
The proposed list of the first set of AOPs to be created, some are more defined than others:
- Reduced mitochondrial activity leads to cholestasis
- Liver fibrosis
- Unfolded protein response-mediated liver toxicity
- Mitotoxicity-mediated hepatotoxicity
- Inhibition of mitochondrial complex I of nigra-striatal neurons leads to parkinsonian motor deficits
- Peripheral neuropathy caused by microtubule interacting drugs
- Oxidative reactivity leads to chemical-induced fanconi syndrome
- Oxidative reactivity leads to acceleration of chronic kidney disease
- Compound accumulation via Megalin/Cubilin uptake leads to acute and chronic kidney disease
- Renal proximal tubular uptake via organic cation transporters leads to...
- Oxidant-induced pulmonary emphysema
- α-diketone-induced bronchiolitis obliterans
- HDAC inhibition leads to neural tube defects
- Cyt p450 inhibition leads to Feminization and Masculinization
- Estrogen/androgen ...
- Oxidative stress-induced hepatoxicity
- Inflammatory cytokine-induced cell death
- HDAC inhibition leads to impaired craniofacial development
Basic strategies and principles for general AOPs are described in this paper:
Villeneuve et al. (2014). Adverse Outcome Pathway (AOP) Development I: Strategies and Principles. Toxicological Sciences PubMed
