Skip to main content
. 2020 Jan 1;10(1):151–165. doi: 10.7150/thno.37098

Table 1.

Values for cytotoxic concentration (IC50, μM) of kinase inhibitors on human pancreatic cancer cell lines, BxPC3, Capan 2, Suit 2 and MIA PaCa-2.

Cell line Drug IC5024h μM (95% CI) IC5048h μM (95% CI) IC5072h μM (95% CI)
BxPC3 crizotinib 15.60 (10.03 - 25.28) 0.005 (indeterminate)* 7.01 (4.67 - 10.29)
cabozantinib 18.99 (13.95 - 27.12) 17.33 (12.08 - 27.05) 13.76 (9.97 - 19.35)
Capmatinib (INC280) indeterminate indeterminate indeterminate
Capan 2 crizotinib 29.25 (26.22 - 32.26) 19.37 (? - 23.31) 12.08 (9.60 - 14.80)
cabozantinib indeterminate 38.20 (?- 66.08) 40.5 (29.90 - 93.93)
capmatinib (INC280) indeterminate indeterminate indeterminate
Suit 2 crizotinib 18.97 (? - 24.03) 13.44 (8.438 - 19.89) 11.46 (9.868 - 13.27)
cabozantinib 25.41 (19.81 - 36.70) 36.66 (26.00 - 63.36) 20.81 (14.10 - 36.80)
capmatinib (INC280) indeterminate indeterminate indeterminate
MIA PaCa-2 crizotinib indeterminate 10.14 (5.787 - 16.21) 6.41 (4.177 - 9.254)
cabozantinib indeterminate indeterminate 14.30 (10.30 - 20.65)
capmatinib (INC280) indeterminate indeterminate indeterminate

IC50: concentration of kinase inhibitors required to reduce cell viability by 50% as compared to the control cells. CI: confidence interval. Estimated using non-linear fit variable slope four parameters, bottom=0, with Graphpad Prism. ? = not available due to poor curve fit. *no range reported by software, suggesting poor fit and unreliable IC50 value. “?” represents no reportable value by software, suggesting poor fit and unreliable IC50 estimate.