Skip to main content
. 2015 Nov 24;2015:798936. doi: 10.1155/2015/798936

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.