| Literature DB >> 29850905 |
Daniel L Villeneuve1, Brigitte Landesmann2, Paola Allavena3, Noah Ashley4, Anna Bal-Price2, Emanuela Corsini5, Sabina Halappanavar6, Tracy Hussell7, Debra Laskin8, Toby Lawrence9, David Nikolic-Paterson10, Marc Pallardy11, Alicia Paini2, Raymond Pieters12, Robert Roth13, Florianne Tschudi-Monnet14.
Abstract
Inflammation is an important biological process involved in many target organ toxicities. However, there has been little consensus on how to represent inflammatory processes using the adverse outcome pathway (AOP) framework. In particular, there were concerns that inflammation was not being represented in a way that it would be recognized as a highly connected, central node within the global AOP network. The consideration of salient features common to the inflammatory process across tissues was used as a basis to propose 3 hub key events (KEs) for use in AOP network development. Each event, "tissue resident cell activation", "increased pro-inflammatory mediators", and "leukocyte recruitment/activation," is viewed as a hallmark of inflammation, independent of tissue, and can be independently measured. Using these proposed hub KEs, it was possible to link together a series of AOPs that previously had no shared KEs. Significant challenges remain with regard to accurate prediction of inflammation-related toxicological outcomes even if a broader and more connected network of inflammation-centered AOPs is developed. Nonetheless, the current proposal addresses one of the major hurdles associated with representation of inflammation in AOPs and may aid fit-for-purpose evaluations of other AOPs operating in a network context.Entities:
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Year: 2018 PMID: 29850905 PMCID: PMC6309953 DOI: 10.1093/toxsci/kfy047
Source DB: PubMed Journal: Toxicol Sci ISSN: 1096-0929 Impact factor: 4.849