Fig. 3From: Metabolic adaptation towards glycolysis supports resistance to neoadjuvant chemotherapy in early triple negative breast cancersMitochondrial oxidative metabolism is decreased in TNBC cells upon treatment with chemotherapy. A–C Oxygen consumption rates (OCR) upon sequential treatment with 1 µM oligomycin, 2 µM FCCP and 0.5 µM rotenone/antimycin A (A), and OCR at basal (B) and maximal levels (C) in HCC1143 cells treated with 9 nM paclitaxel or 600 nM epirubicin for 24 h. D–I OCR values in HCC38 (D–F) and HCC1937 (G–I) in the same experimental conditions than indicated for HCC1143 cells (except that 4 and 300 nM paclitaxel as well as 25 and 800 nM epirubicin were used for HCC38 and HCC1937 cells, respectively). Data are plotted as the means ± SEM from n = 6 cultures, performed each time with ≥ 3 technical replicates (A–I). Significance was determined by one-way ANOVA (B, C, E, F, and H, I) with Tukey’s multiple comparison test. *p < 0.05; **p < 0.01; ***p < 0.001; ns, not significantBack to article page