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. 2019 Aug 22;20(17):4095. doi: 10.3390/ijms20174095

Table 2.

MK-8776-sensitized doxorubicin and paclitaxel in SW620/Ad300 cells.

Compounds IC50 ± SD a (μM) (RF b)
SW620 SW620/Ad300
Doxorubicin 0.031 ± 0.014 (1.00) 9.950 ± 2.023 (320.97)
+ MK-8776 (0.3 μM) 0.028 ± 0.016 (0.90) 1.362 ± 0.122 (43.94) *
+ MK-8776 (1 μM) 0.035 ± 0.012 (1.13) 0.426 ± 0.184 (13.74) *
+ Verapmil (3 μM) 0.038 ± 0.021 (1.23) 0.096 ± 0.023 (3.10) *
Paclitaxel 0.091 ± 0.015 (1.00) 21.19 ± 6.25 (232.86)
+ MK-8776 (0.3 μM) 0.076 ± 0.038 (0.84) 1.784 ± 0.125 (19.60) *
+ MK-8776 (1 μM) 0.074 ± 0.003 (0.81) 0.597 ± 0.566 (6.56) *
+ Verapamil (3 μM) 0.113 ± 0.006 (1.24) 0.639 ± 0.023 (7.03) *
Cisplatin 1.481 ± 0.676 (1.00) 1.514 ± 0.398 (1.02)
+ MK-8776 (0.3 μM) 1.329 ± 0.156 (0.90) 1.423 ± 0.438 (0.94)
+ MK-8776 (1 μM) 1.228 ± 0.181(0.83) 1.266 ± 0.295 (0.84)
+ Verapamil (3 μM) 1.164 ± 0.107 (0.79) 1.851 ± 0.364 (1.25)

* p < 0.05 vs. control. a Three independent experiments that were performed in triplicate. b IC50 values of substrates in the resistant cell lines in the presence or absence of MK-8776 or verapamil divided by the IC50 values of substrates in the parental cells without MK-8776 or verapamil.