Fig. 6From: A systematic flux analysis approach to identify metabolic vulnerabilities in human breast cancer cell linesInhibition of glutamine oxidation reduced Hs578T cell viability. a Cell viability in Hs578T cells treated with 3 μM BPTES for 2 days. b Cell viability in MCF10a cells treated with 3 μM BPTES for 2 days. c AMPK-mTORC1 signalling in Hs578T cells treated with 3 μM BPTES for 2 days. All data are mean ± SEM, n = 3–4 biological replicates/group. *p < 0.05 vs. vehicleBack to article page