| Literature DB >> 25070415 |
Ted W Simon1, S Stoney Simons, R Julian Preston, Alan R Boobis, Samuel M Cohen, Nancy G Doerrer, Penelope A Fenner-Crisp, Tami S McMullin, Charlene A McQueen, J Craig Rowlands.
Abstract
The HESI RISK21 project formed the Dose-Response/Mode-of-Action Subteam to develop strategies for using all available data (in vitro, in vivo, and in silico) to advance the next-generation of chemical risk assessments. A goal of the Subteam is to enhance the existing Mode of Action/Human Relevance Framework and Key Events/Dose Response Framework (KEDRF) to make the best use of quantitative dose-response and timing information for Key Events (KEs). The resulting Quantitative Key Events/Dose-Response Framework (Q-KEDRF) provides a structured quantitative approach for systematic examination of the dose-response and timing of KEs resulting from a dose of a bioactive agent that causes a potential adverse outcome. Two concepts are described as aids to increasing the understanding of mode of action-Associative Events and Modulating Factors. These concepts are illustrated in two case studies; 1) cholinesterase inhibition by the pesticide chlorpyrifos, which illustrates the necessity of considering quantitative dose-response information when assessing the effect of a Modulating Factor, that is, enzyme polymorphisms in humans, and 2) estrogen-induced uterotrophic responses in rodents, which demonstrate how quantitative dose-response modeling for KE, the understanding of temporal relationships between KEs and a counterfactual examination of hypothesized KEs can determine whether they are Associative Events or true KEs.Entities:
Keywords: Q-KEDRF; associative event; key event; mode of action; modulating factor; risk assessment
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Year: 2014 PMID: 25070415 DOI: 10.3109/10408444.2014.931925
Source DB: PubMed Journal: Crit Rev Toxicol ISSN: 1040-8444 Impact factor: 5.635