Kinetic studies of the effects of Temodal and quercetin on astrocytoma cells

The aim of the present study was to investigate the kinetics of the effects exerted by temodal and quercetin on the survival of the human astrocytoma moggccm cell line. our results indicate that quercetin was toxic and induced necrosis,whereas temodal induced autophagy-mediated cell death most effectively. the amount of cell death directly correlated with drug concentration and length of exposure. during combined administration of both drugs,temodal attenuated the cytotoxic effects of quercetin. combinations of both drugs were effective in inducing programmed cell death,but the type of cell death was concentration-dependent. co-administration of temodal (100 μm) with a low quercetin concentration (5 μm) resulted in a very significant induction of autophagy; however,after treatment with quercetin at a higher concentration (30 μm),apoptosis became the primary mechanism of cell death. the sequence of drug administration was also important. the highest number of dead cells was observed after simultaneous administration of both drugs or after pre-incubation with temodal followed by treatment with quercetin. apoptosis was identified through activation of the mitochondrial pathway including cleavage of caspase-3 and release of cytochrome c. autophagy was identified through increased levels of lc3ii. our results indicate that temodal and quercetin are synergistic inducers of programmed cell death,better together than applied separately. this drug combination appears to be a potent and promising therapeutic relevant to the treatment of gliomas. copyright © by institute of pharmacology polish academy of sciences.