Figure 1.

Inhibition of cell proliferation induced by hydroethanolic extract of C. album leaves (ECAL) in MDA-MB-231 and MCF-12A cells. Cells were treated with increasing concentrations of ECAL (1.7–1730 μg/mL) for (A) 24 h, (B) 48 h and (C) 72 h. Label-free kinetic live monitoring of cell proliferation was performed using a LionheartFX automated microscope with the direct image acquisition of cells in microplates at 0, 24, 48 and 72 h of the post-addition of the tested compounds.