Using Quantitative Systems Toxicology to Investigate Observed Species Differences in CKA-Mediated Hepatotoxicity

Author:

Battista Christina12ORCID,Yang Kyunghee1,Stahl Simone H3ORCID,Mettetal Jerome T4,Watkins Paul B2,Siler Scott Q1,Howell Brett A15

Affiliation:

1. DILIsym Services, Inc., Research Triangle Park, North Carolina

2. Division of Pharmacotherapy and Experimental Therapeutics, UNC Institute for Drug Safety Sciences, UNC Eshelman School of Pharmacy, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina

3. Safety and ADME Translational Sciences, Drug Safety and Metabolism, IMED Biotech Unit, Astra Zeneca R&D, Cambridge CB4 0WG, UK

4. Safety and ADME Translational Sciences, Drug Safety and Metabolism, IMED Biotech Unit, Astra Zeneca R&D, Waltham, Massachusetts

5. DILIsym Services, Inc., Six Davis Drive, PO BOX 12317, Research Triangle Park, NC 27709

Funder

DILI-sim Initiative

Research Participation Program at the Center for Drug Evaluation and Research

U.S. Food and Drug Administration

Oak Ridge Institute for Science and Education

U.S. Department of Energy and Food and Drug Administration

Publisher

Oxford University Press (OUP)

Subject

Toxicology

Reference29 articles.

1. Hepatotoxicity in drug development: detection, significance and solutions;Ballet;J. Hepatol,1997

2. Modeling drug- and chemical-induced hepatotoxicity with systems biology approaches;Bhattacharya;Front Physiol,2012

3. Angiogenesis and chemokines in rheumatoid arthritis and other systemic inflammatory rheumatic diseases;Bodolay;J Cell Mol Med,2002

4. Intracellular drug concentrations and transporters: measurement, modeling, and implications for the liver;Chu;Clin Pharmacol Ther,2013

5. A combined in vitro approach to improve the prediction of mitochondrial toxicants;Eakins;Toxicol In Vitro,2016

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