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. 2016 Aug 12;17(10):1094–1106. doi: 10.1080/15384047.2016.1219820

Figure 1.

Figure 1.

(A) Romidepsin alone inhibited cell viability in a time- and dose-dependent manner in Hut-78 and Karpas-299 cells (see Table 1 for IC50 values of romidepsin). (B) Lenalidomide alone slightly inhibited cell viability in TCL cell lines, but did not reach the IC50 even after 72 h of treatment. (C) Isobologram analysis of combination treatment with both romidepsin (0.5, 1, 2.5 nM) and lenalidomide (2, 4, 10 µM) for 24 hours (see Table 2 for combination index values) and cell viability from cell lines treated with romidepsin (2.5 nM) and lenalidomide (10 µM) either alone and in combination for 24 hours (*P < 0.003; **P < 0.001; ***P < 0.02; ****P < 0.002). (D) Cell viability from PBMCs from 3 healthy subjects treated with romidepsin (2.5 nM) and lenalidomide (10 µM) alone and in combination. (E) Cytotoxicity of TCL cells after treatment with romidepsin (2.5 nM) for 6 hours followed by washout and the addition of lenalidomide (10 µM) for 24 hours.