Skip to main content
. 2011 Oct 15;15(8):2175–2184. doi: 10.1089/ars.2010.3378

FIG. 2.

FIG. 2.

Suppression of RAGE expression by shRNA increases pancreatic tumor cell sensitivity to oxidative injury. (A) Suppression of RAGE expression increases H2O2-induced oxidative cytotoxicity. After transfection with RAGE shRNA or control shRNA for 48 h, Panc2.03 and Panc02 cells were treated with H2O2 at indicated dose for 24 h and then the cell viability was analyzed (n = 3, *p < 0.05 versus control shRNA group). A representative Western blot of RAGE level after shRNA is depicted (inset). (B) NF-κB inhibitors increase H2O2-induced oxidative injury. Panc2.03 and Panc02 cells were treated with H2O2 (0.25 mM) for 24 h with or without NF-κB inhibitors: Bay 11-7085 (“Bay”, 10 μM) and curcumin (50 μM), and the cell viability was analyzed (n = 3, #p < 0.05 versus control shRNA group, *p < 0.05 versus H2O2 group).