We have previously reported that the pro-apoptotic pyrrolobenzoxazepine, PBOX-6, induces apoptosis in chronic myelogenous
leukaemia (CML) cells which is accompanied by oligonucleosomal DNA fragmentation. In this study we show that PBOX-6-induced
oligonucleosomal DNA fragmentation occurs in the absence of caspase and CAD activation in CML cells. Dissection of the signalling
pathway has revealed that induction of apoptosis requires the upstream activation of a trypsin-like serine protease that promotes
the phosphorylation and inactivation of anti-apoptotic Bcl-2. In addition, in this system chymotrypsin-like serine proteases
are dispensable for high molecular weight DNA fragmentation, however are required for the activation of a relatively small
manganese-dependent acidic endonuclease that is responsible for oligonucleosomal fragmentation of DNA. Furthermore, we demonstrate
mitochondrial involvement during PBOX-6-induced apoptosis and suggest the existence of unidentified mitochondrial effectors
of apoptosis.
Keywords Caspase-independent - Pyrrolobenzoxazepine - Apoptosis - Serine proteases - Endonuclease
This work was supported by the Irish Research Council for Science, Technology and Engineering (IRCSET).