Fig. 1From: Short term starvation potentiates the efficacy of chemotherapy in triple negative breast cancer via metabolic reprogrammingDifferential sensitivity of cancer cells to STS and DXR is associated with enhanced ROS production in triple negative breast cancer cells. a Starvation in combination with 100 nM DXR treatment selectively inhibits cellular proliferation (Hoechst) in MDA-MB-231, MDA-MB-468 and HS578 cancer cells but not in the near normal MCF-10 cell line. Scale bar: 1 mm. b Starvation in combination with 100 nM DXR treatment selectively increases cell death (PI) in MDA-MB-231, MDA-MB-468 and HS578 cancer cells but not in the near normal MCF-10 cell line. c Assessment of intracellular ROS production. Data are presented as mean of the fold change ± SD of intracellular ROS production in MDA-MB-231, MDA-MB-468 and HS578 and MCF-10A cells upon STS, DXR or combined STS + DXR treatment. *P ≤ 0.05. d Assessment of intracellular ROS production. Data are presented as mean of the fold change ± SD in MDA-MB-231 cells treated with STS with or without the MTH1 inhibitor TH1579. *P ≤ 0.05Back to article page