Figure 1.
Figure 1. Effects of CC-5013, rapamycin, and their combination on proliferation of MM cell lines and PBMCs. (A) Time- and dose-dependent inhibition of proliferation in sensitive MM cell lines (MM1.S, OPM2, SB645), demonstrated by measuring thymidine [3H-TdR] uptake during the last 8 hours of 48-hour cultures, in the presence of CC-5013 (μM), rapamycin (nM), or both in fixed-dose treatment. (B) Time- and dose-dependent inhibition of proliferation demonstrated by MTT in MM1.S cells. (C) Inhibition of DNA synthesis as measured by 3H-TdR uptake in resistant MM cell lines treated with CC-5013 and rapamycin. (D) Lack of toxicity of combined therapy on PBMCs, demonstrated by MTT assay. Error bars indicate one standard deviation.

Effects of CC-5013, rapamycin, and their combination on proliferation of MM cell lines and PBMCs. (A) Time- and dose-dependent inhibition of proliferation in sensitive MM cell lines (MM1.S, OPM2, SB645), demonstrated by measuring thymidine [3H-TdR] uptake during the last 8 hours of 48-hour cultures, in the presence of CC-5013 (μM), rapamycin (nM), or both in fixed-dose treatment. (B) Time- and dose-dependent inhibition of proliferation demonstrated by MTT in MM1.S cells. (C) Inhibition of DNA synthesis as measured by 3H-TdR uptake in resistant MM cell lines treated with CC-5013 and rapamycin. (D) Lack of toxicity of combined therapy on PBMCs, demonstrated by MTT assay. Error bars indicate one standard deviation.

Close Modal

or Create an Account

Close Modal
Close Modal