Table 3.
Uptake of radiolabeled compounds in the presence of 10 μM Verapamil
| A431
|
NCI/Adr
|
|||
|---|---|---|---|---|
| − Verapamil | + Verapamil* | − Verapamil | + Verapamil | |
| Paclitaxel (70 nM) | 34.2 ± 0.8† | 7‡ | 2.2 ± 0.2 | 404 |
| pED (70 nM) | 19.0 ± 0.6 | 82 | 8.3 ± 0.8 | 306 |
| pEB (70 nM) | 58.7 ± 2.7 | 2 | 49.0 ± 1.1 | 5 |
| Paclitaxel (3.5 nM) | 3.3 ± 0.1 | −14 | 0.1 ± 0.0 | 188 |
| pED (3.5 nM) | 0.6 ± 0.0 | 174 | 0.2 ± 0.0 | 795 |
| pEB (3.5 nM) | 3.9 ± 0.1 | 22 | 4.7 ± 0.2 | 122 |
Tumor cells were incubated for 2 h with the indicated concentrations of tritiated compounds in the presence or absence, respectively, of 10 μM Verapamil. After washing, cells were solubilized and the radioactivity measured and normalized to the cell numbers.
10 μM Verapamil.
Mean ± SD (pmol/106 tumor cells).
Percent of additional uptake in the presence of Verapamil.