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. 2024 Jan 2;43:4. doi: 10.1186/s13046-023-02879-8

Fig. 3.

Fig. 3

ABCB1 inhibition restores PR cell lines paclitaxel sensitivity. Representative confocal images of PDAC PR cell lines treated O/N with either 10 μM verapamil or DMSO as a control and stained with 1 μg/mL of Hoechst33342 for 2 h at 37 °C in growth medium. Scale bar: 100 μm. Quantification of Hoechst signal total intensity with CellProfiler upon DMSO (red) or 10 μM verapamil (green) treatment. Representative growth curves of the 3 PR resistant cell models exposed for 72 h to paclitaxel concentration ranges, combined with 0.1% DMSO (red triangles), 5 μM verapamil (black diamonds) or 10 μM verapamil (green squares). Mean and SD of triplicates is shown. Concentrations of paclitaxel causing 50% reduction in cell growth determined in absence or presence of 5 μM or 10 μM verapamil. Mean ± SEM for 3 independent experiments is displayed. As 50% growth inhibition was not fully reached in PR cells exposed to only paclitaxel, values from Supplemental Table S2 are displayed. Relative proliferation (compared to siKINASEpool control) of Patu-T PR cells 72 h post-treatment with the indicated siRNA SMARTpools (50 nM) and paclitaxel concentrations, analyzed by SRB assay. Verapamil is used as positive control for ABCB1 inhibition