TY - JOUR T1 - <strong>Quantitative CYP3A4 induction risk assessment using human hepatocytes complemented with pregnane X receptor (PXR)-activating profiles </strong> JF - Drug Metabolism and Disposition JO - Drug Metab Dispos DO - 10.1124/dmd.122.001132 SP - DMD-AR-2022-001132 AU - Aynur Ekiciler AU - Wen Li Kelly Chen AU - Yan Bo AU - Alessandra Pugliano AU - Massimiliano Donzelli AU - Neil Parrott AU - Kenichi Umehara Y1 - 2022/01/01 UR - http://dmd.aspetjournals.org/content/early/2022/12/02/dmd.122.001132.abstract N2 - Reliable in vitro to in vivo translation of CYP3A4 induction potential is essential to support risk mitigation for compounds during pharmaceutical discovery and development. In this study, a linear correlation of CYP3A4 mRNA induction potential in human hepatocytes with the respective PXR activation in a reporter gene assay using DPX2 cells was successfully demonstrated for 13 clinically used drugs. Based on this correlation, using rifampicin as a positive control, the magnitude of CYP3A4 mRNA induction for 71 internal compounds at several concentrations up to 10 µM (n=90), was predicted within 2-fold error for 64% of cases with only a few false positives (19%). Furthermore, the in vivo AUC reduction of probe CYP substrates was reasonably predicted for 8 marketed drugs (carbamazepine, dexamethasone, enzalutamide, nevirapine, phenobarbital, phenytoin, rifampicin and rufinamide) using the static net effect model using both the PXR activation and CYP3A4 mRNA induction data. The liver exit concentrations were used for the model in place of the inlet concentrations to avoid false positive predictions and the concentration achieving 2-fold induction (F2) was used to compensate for the lack of full induction kinetics due to cytotoxicity and solubility limitations in vitro. These findings can complement the currently available induction risk mitigation strategy and potentially influence the drug interaction modeling work conducted at clinical stages. Significance Statement The established correlation of CYP3A4 mRNA in human hepatocytes to PXR activation provides a clear cut-off to identify a compound showing an in vitro induction risk, complementing current regulatory guidance. Also, the demonstrated in vitro-in vivo translation of induction data strongly supports clinical development program although limitations remain for drug candidates showing complex disposition pathways such as involvement of auto-inhibition/induction, active transport and high protein binding. ER -