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. Author manuscript; available in PMC: 2020 Aug 1.
Published in final edited form as: Mol Cancer Ther. 2019 May 29:10.1158/1535-7163.MCT-18-1258. doi: 10.1158/1535-7163.MCT-18-1258

Figure 2.

Figure 2.

EC359 decrease cell viability, colony formation, invasion and promote apoptosis of TNBC cells that express LIF and LIFR. The expression of LIF and LIFR in TNBC (A), ER+ BC and normal mammary epithelial cells (B) was determined by western blotting. Effect of increasing doses of EC359 on the cell viability of TNBC (C) ER+BC and normal mammary epithelial cells (D) was determined using the MTT cell viability assay (n=3). E, Effect of inducible CRISPR/Cas9 mediated KO of LIFR on EC359 induced cell viability was determined using MTT assays in BT-549 cells (n=3). F, Effect of EC359 (20 nM) on cell survival was measured using colony formation assays. G, Effect of EC359 (25 nM) on cell invasion of MDA-MB-231 and BT-549 model cells was determined using matrigel invasion chamber assays (n=3). Representative images of invaded cells are shown and the number of invaded cells in five random fields was quantitated. H, Effect of indicated doses of EC359 on caspase 3/7 activity (Caspase-Glo3/7 assay) and I, Annexin V staining in MDA-MB-231 and BT-549 cells (n=3) was determined. ** P<0.01, ****p<0.0001.