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. 2021 Jun 25;4:799. doi: 10.1038/s42003-021-02215-w

Fig. 5. The cell viability and MCL1/BCL-2 protein expression analysis in MV4-11/MOLM-13 Midostaurin-resistant cells treated with the triple combination Eht1864/Venetoclax/Midostaurin.

Fig. 5

a BCL-2 and MCL1 protein expression analysis in MV4-11/MOLM-13 MID-Res compared to MID-Sens cells, in MV4-11/MOLM-13 MID-Res ± 50 nM Mid compared to MID-Sens ± 50 nM Mid. b Venetoclax (Ve) IC50 analysis in MV4-11/MOLM-13 MID-Sens and MID-Res cells treated with Ve during 48 h. c BCL-2 and MCL1 protein expression analysis in MV4-11/MOLM-13 MID-Res treated with Mid and Eht alone/combination. d Cell viability and synergy analysis in MV4-11/MOLM-13 MID-Res treated with Mid, Ve, and Eht alone/combination during 48 h. e BCL-2 and MCL1 protein expression and cell death analysis (Annexin V + /PI- + Annexin V + PI+) in DMSO (control), Mid (p = 0.76, t = 0.34, df = 2.3), Ve (p = 0.054, t = 2.7, df = 3.6), Eht (p < 0.05, 3.1, df = 3.7) and Mid + Eht (p < 0.01, t = 10.29, df = 3) Mid + Ve (p < 0.01, t = 8, df = 3.8) Ve + Eht (p < 0.001, t = 14, df = 3.9) and Eht + Ven + Mid (p < 0.001, t = 16.1, df = 3.2) during 24 h. f Cell death analysis by flow cytometry in REF001/REF002 AML samples and in PBMCs obtained from Healthy Donors HD4/HD5/HD6 treated with Mid, Eht, and Ve alone/combination during 24 h. The western blot results are normalized by loading control (GAPDH) and are expressed as fold change relative to the control. Data are shown as means ± SDs (error bars) from three independent experiments.