Determination of CYP3A4 Inducing Properties of Compounds Using a Laboratory-Developed Cell-Based Assay

Int J Toxicol. 2015 Sep-Oct;34(5):454-68. doi: 10.1177/1091581815599335. Epub 2015 Aug 12.

Abstract

A cell-based assay to measure cytochrome P450 3A4 (CYP3A4) induction was developed to screen for potential CYP3A4 inducers. This 96-well format assay utilizes HepG2 cells transfected with a gene construct of CYP3A4 proximal promoter linked to green fluorescence protein (GFP) gene, and the expression of the GFP is then measured quantitatively. Bergamottin at 5 to 25 µmol/L produced low induction relative to the positive control. Both curcumin and lycopene were not found to affect the expression of GFP, suggesting no induction properties toward CYP3A4. Interestingly, resveratrol produced significant induction from 25 µmol/L onward, which was similar to omeprazole and may warrant further studies. In conclusion, the present study demonstrated that this cell-based assay can be used as a tool to evaluate the potential CYP3A4 induction properties of compounds. However, molecular docking data have not provided satisfactory pointers to differentiate between CYP3A4 inducers from noninducers or from inhibitors, more comprehensive molecular screening may be indicated.

Keywords: CYP3A4 induction; cell-based assay; drug–drug interaction; drug–herb interaction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Assay*
  • Cytochrome P-450 CYP3A / biosynthesis*
  • Cytochrome P-450 CYP3A / genetics
  • Cytochrome P-450 Enzyme Inducers / pharmacology*
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Hep G2 Cells
  • Humans
  • Laboratories
  • Molecular Docking Simulation
  • Promoter Regions, Genetic

Substances

  • Cytochrome P-450 Enzyme Inducers
  • Green Fluorescent Proteins
  • Cytochrome P-450 CYP3A
  • CYP3A4 protein, human