Figure 5
Figure 5. MKC-3946 enhances MM cytotoxicity of bortezomib or 17-AAG, even in the presence of BMSCs or exogenous IL-6. (A-B) INA6 cells were treated with bortezomib (A) or 17-AAG (B) in combination with MKC-3946 0μM (□), 5μM (▩), or 10μM (■), in the presence or absence of BMSCs for 48 hours. (C-D) INA6 cells were treated with bortezomib (C) or 17-AAG (D) in combination with MKC-3946 0μM (□), 5μM (▩), or 10μM (■), with 2.5 ng/mL or 10 ng/mL of IL-6 for 48 hours. Cell proliferation was assessed by [3H]-thymidine uptake of quadruplicate cultures. Data represent the mean ± SD of [3H]-thymidine incorporation (CPM).

MKC-3946 enhances MM cytotoxicity of bortezomib or 17-AAG, even in the presence of BMSCs or exogenous IL-6. (A-B) INA6 cells were treated with bortezomib (A) or 17-AAG (B) in combination with MKC-3946 0μM (□), 5μM (▩), or 10μM (■), in the presence or absence of BMSCs for 48 hours. (C-D) INA6 cells were treated with bortezomib (C) or 17-AAG (D) in combination with MKC-3946 0μM (□), 5μM (▩), or 10μM (■), with 2.5 ng/mL or 10 ng/mL of IL-6 for 48 hours. Cell proliferation was assessed by [3H]-thymidine uptake of quadruplicate cultures. Data represent the mean ± SD of [3H]-thymidine incorporation (CPM).

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