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. 2022 Mar 15;12(3):1102–1115.

Figure 2.

Figure 2

High throughput drug screening to identify candidates for overcoming venetoclax resistance. (A) Schematic illustration of the high-throughput drug screen. The drug screen was performed over a library consisting of 320 drugs in two parental and venetoclax-resistant paired cell lines by a 72 h cell viability test with one dose (5 μM) as first round screen followed by 2nd round drug validation via 4-dose viability assay in the same cell lines to identify the top candidates in overcoming venetoclax resistance. (B) 1st round drug screen at 5 μM by a cell viability inhibition assay in Mino, Mino-Re, Rec-1 and Rec1-Re cells. Each treatment for the cell viability assay was set up in triplicate. Relative cell viability was normalized to DMSO control. Cell viability less than 20% was considered as positive (red box). (C) 2nd round drug validation for the top candidates (six drugs) was performed by a four-dose (three-fold dilution) cell viability assay at 72 h in the same cell lines. The heatmap shown represents the IC50 values (µM). Each treatment for the cell viability assay was set up in triplicate and the experiment was repeated three times.