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The proliferation of MCF7 (breast cancer cells) was inhibited by DAP without cell toxicity. a Effect of DAP on the proliferation of MCF7 cells was measured up to 3 days. DAP was treated in triplicate at each concentration. b Effect of DAP on the viability of MCF7 cells was investigated by using a trypan blue staining assay (p = 0.003, one-way ANOVA). c The growth rates from (a) (t = 3 d) plotted against log[DAP]. 100% equal the growth rate of untreated cells
