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. Author manuscript; available in PMC: 2021 Jul 19.
Published in final edited form as: Assay Drug Dev Technol. 2016 Sep 22;14(8):489–510. doi: 10.1089/adt.2016.727

Figure 2. Graphical representation of IC50 values of Prestwick Library Hits in MCF7-Casp3 and MCF7-Bcl2.

Figure 2

MCF7-Casp3 and MCF7-Bcl2 cells were exposed to the 51 compound selected in the primary screen. Cells were treated with 8 different concentrations for 24hs and cell death was measured with the HT PI Cytotoxicity Assay. The percentage of dead cells was plotted with GraphPad Prism 5.0 to calculate the LC50 values. Top-left panel. Graphic representation of the calculated LC50 for each compound on both cell lines. The solid black line correspond to an artificial line with slope = 1 representing the ideal situation where the LC50 is identical on both cell lines. Green dots = LC50 for siramesine calculated form 9 concertation-response curves distributed across the screen plates, blue dots = LC50 for staurosporine, black dots = LC50 for Prestwick library Hits, red dots= LC50 for Prestwick library Hits for which concertation-response curves are showed in the middle and bottom panels. The similar LC50 in both cell lines suggest that cell death induced by most of this compound is indeed Casp3 independent (see also Figure S3). The top-right panel. Concertation-response curves for siramesine (average of 9 curves) and staurosporine. LC50 ± 95% CI are shown. LC50 values for siramesine in both cell lines were compared with an F-test and show no significant difference (p-value = 0.48). Middle and bottom panel. Concertation-response curves for representative compound. LC50 ± 95% CI are shown. F-test and show no significant difference (p-value = > 0.05). The curves for the other compounds are shown in Figure S2.