Activation of Nrf2 and Noxa up-regulation by ATO are not mediated by
ATO-induced ROS. A, KMS11 was incubated with 100 μm
BHA for 16 h. Control and BHA-treated cells were then treated with 1
μm ATO for 6 h. DHE was used for ROS determination. The
shaded histogram represents untreated cells while the bold-lined
open histograms represent the indicated treatment. B, KMS11 was
treated as in A and protein lysates were subjected to Western blot
analysis of HO-1, NQO1, Nrf2, Keap1, Noxa, and actin. C, KMS11 was
treated as in A, and cell viability was measured by Annexin-V-FITC/PI
staining after 48 h of ATO treatment. Percent (%) of control viability was
calculated, and data are presented as mean ± S.D. of four independent
experiments.