CD95 and TRAIL receptor-mediated activation of protein kinase C and NF-kappa B contributes to apoptosis resistance in ductal pancreatic adenocarcinoma cells

The molecular alterations in tumour cells leading to resistance towards apo ptosis induced by CD95 and TRAIL-receptors are not fully understood. We rep ort here that the stimulation of the CD95- and TRAIL-resistant human pancre atic adenocarcinoma cell line PancTuI with an agonistic anti-CDW antibody o r TRAIL resulted in activation of protein kinase C and NF-kappaB, Inhibitio n of protein kinase C by Go6983 sensitized these cells to apoptotic challen ges and strongly diminished activation of NF-kappaB by anti-CD95 and TRAIL. Similarly, inhibition of NF-kappaB by MG132 or by transient transfection w ith a dominant negative mutant of I kappaB alpha restored the responsivenes s of PancTuI cells to both death ligands. In the CD95 and TRAIL-sensitive c ell line Colo357 the induction of protein kinase C and NF-KB following acti vation of CD95 and TRAIL-R was very moderate compared with PancTuI cells. H owever, pre-incubation of these cells with PMA strongly reduced their apopt otic response to anti-CD95 and TRAIL. Taken together, we show that activati on of protein kinase C operates directly in a death receptor-dependent mann er in PancTuI cells and protect pancreatic tumour cells from anti-CD95 and TRAIL-mediated apoptosis by preventing the loss Delta Psim and Cytochrome c release as well as by induction of NF-kappaB.