Table 1.
Cell lines examined and EGFR turnover rate (t 1/2).
| Cell line | Mutation | Cell doubling time (hrs) | Compound | Inhibitor conc. (nM) | Turnover (t 1/2 hrs) |
|---|---|---|---|---|---|
| A431 | WT | 31 | N/A | 28 | |
| H3255 | L858R | 42 | N/A | 10 | |
| H1975 | L858R T790M | 23 | N/A | 9.2 | |
| PC-9 | Del 746–750 | 16 | DMSO | 0 | 7.5 |
| PC-9 | Del 746–750 | N/A | Dacomitinib | 18 | 5.8–9.1 |
| PC-9 | Del 746–750 | N/A | Compound A | 360 | 6.9–12 |
One wild-type and three mutant EGFR cell lines were analyzed. Cell lines with wild-type EGFR (A431), EGFR with a single activating mutant Del 746–750 (PC-9) or L858R (H3255), and the drug-resistant double mutant L858R/T790M (H1975) EGFR had turnover rate half-lives from 28 to 7.5 hours. These rates were not adjusted for amino acid recycling effects. The EGFR turnover rate half-lives in PC-9 cells dosed with inhibitors compound A and dacomitinib were reported as a range to include impact of cell viability on the measurement.