کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5861473 | 1133760 | 2015 | 7 صفحه PDF | دانلود رایگان |
- Assays for human AhR, CAR and PXR ligand screening have been improved and validated.
- Reverse transfection is a robust and reproducible method for xenosensor activation.
- The assays can be used to predict CYP induction in early drug discovery.
Discovery of receptor-dependent mechanisms for regulation of drug metabolism has provided a new way to evaluate the propensity of drug candidates to cause induction of cytochrome P450 enzymes. Therefore, receptor-based reporter assays have become common in early stages of drug development projects and in mechanistic studies. Here, we report a reverse transfection system to conduct activation assays for human xenosensors AhR, CAR and PXR. The assay format is based on long-term stability and uniformity of DNA/carrier complexes on culture plates, avoiding multiple stages and variation inherent in conventional transfection methods. Consequently, these improved assays are streamlined, reproducible and formally validated with Zâ² factors exceeding 0.5. This novel reverse transfection system is expected to find use in diverse areas of early drug development such prediction of CYP induction, evaluation of species differences and in mechanistic studies.
Journal: Toxicology in Vitro - Volume 29, Issue 7, October 2015, Pages 1759-1765