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. 2011 Oct 13;3(10):839–857. doi: 10.3390/nu3100839

Figure 2.

Figure 2

(a) Intracellular reactive oxygen species (ROS) in breast cells treated for 24 h with HT or TY; (b) Increase of the cellular ROS level after an oxidative burn with H2O2; (c) Intracellular ROS in breast cells treated for 24 h with HT or TY followed by an oxidative burst with H2O2. Inhibitory effects of HT and TY are shown as percent inhibition of untreated or H2O2-stimulated fluorescence and represented as the mean ± SEM of three independent replicates carried out in triplicate. MCF7; MDA-MB-231; * MCF10A indicates significant differences.