Figure 2
Figure 2. Zalypsis overcomes the protective effects of IL-6, IGF-I, and adherence to patient BMSCs. (A,B) MM1S cells were treated for 48 hours with the indicated concentrations of Zalypsis in the presence or absence of IL-6 (A) or IGF-I (B), and DNA synthesis was determined by measuring BrdU incorporation during the last 8 hours of 48-hour cultures. (C) MM1S-luc cells were treated for 48 hours with the indicated concentrations of Zalypsis in the presence or absence of BMSCs derived from a MM patient, and proliferation was analyzed by bioluminescence (photons/sec). (D) BMSCs were cultured with different doses of Zalypsis for 48 hours, and the cytotoxicity was analyzed by MTT assay. Data are mean plus or minus SD of quadruplicates.

Zalypsis overcomes the protective effects of IL-6, IGF-I, and adherence to patient BMSCs. (A,B) MM1S cells were treated for 48 hours with the indicated concentrations of Zalypsis in the presence or absence of IL-6 (A) or IGF-I (B), and DNA synthesis was determined by measuring BrdU incorporation during the last 8 hours of 48-hour cultures. (C) MM1S-luc cells were treated for 48 hours with the indicated concentrations of Zalypsis in the presence or absence of BMSCs derived from a MM patient, and proliferation was analyzed by bioluminescence (photons/sec). (D) BMSCs were cultured with different doses of Zalypsis for 48 hours, and the cytotoxicity was analyzed by MTT assay. Data are mean plus or minus SD of quadruplicates.

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