Figure 7
Figure 7. Efficacy of CBS9106 in human MM xenograft models. Subcutaneous tumor growth curves (A) and the body weight change (B) of subcutaneous xenograft model of RPMI-8226 (n = 8). Mice were treated orally with vehicle (Gum Arabic, ●) or CBS9106 (31.25 mg/kg, 5 times weekly, □; 62.5 mg/kg, 5 times weekly, ▵; or 125 mg/kg, 3 times weekly, ○) for 2 weeks. (C) Tumors from RPMI-8226 cell xenografts were harvested at 24 or 48 hours from the mice treated orally with vehicle (Gum Arabic, Gum) or CBS9106 (125 mg/kg, A-C). Protein extracts prepared from the tumors were analyzed by immunoblotting to detect indicated proteins. (D) Survival analysis of the MM.1S xenograft model mice (n = 10) with oral CBS9106 treatment (125 mg/kg, 3 times weekly, dotted line) for 2 weeks. (E) Body weight change for panel D. Error bars represent SE.

Efficacy of CBS9106 in human MM xenograft models. Subcutaneous tumor growth curves (A) and the body weight change (B) of subcutaneous xenograft model of RPMI-8226 (n = 8). Mice were treated orally with vehicle (Gum Arabic, ●) or CBS9106 (31.25 mg/kg, 5 times weekly, □; 62.5 mg/kg, 5 times weekly, ▵; or 125 mg/kg, 3 times weekly, ○) for 2 weeks. (C) Tumors from RPMI-8226 cell xenografts were harvested at 24 or 48 hours from the mice treated orally with vehicle (Gum Arabic, Gum) or CBS9106 (125 mg/kg, A-C). Protein extracts prepared from the tumors were analyzed by immunoblotting to detect indicated proteins. (D) Survival analysis of the MM.1S xenograft model mice (n = 10) with oral CBS9106 treatment (125 mg/kg, 3 times weekly, dotted line) for 2 weeks. (E) Body weight change for panel D. Error bars represent SE.

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