PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 16048438-13 2005 DN-STAT3 induced the activation of caspase-3 and PARP [poly(ADP-ribose) polymerase] cleavage in polyamine-depleted cells. Polyamines 96-105 caspase 3 Homo sapiens 35-44 20940027-6 2011 Increase of the Bax/Bcl-2 ratio and activation of caspase-3 might be due to intracellular polyamine depletion. Polyamines 90-99 caspase 3 Homo sapiens 50-59 15024023-7 2004 Inactivation of Akt by either treatment with LY294002 or ectopic expression of a dominant negative Akt mutant (DNMAkt) not only enhanced the caspase-3 activation in polyamine-deficient cells but also prevented the increased resistance to tumor necrosis factor-alpha/cycloheximide-induced apoptosis. Polyamines 165-174 caspase 3 Homo sapiens 141-150 15941855-7 2005 The effect of polyamine depletion on caspase-3 activity was evaluated in BMSCs after treatment with 500 U/ml tumor necrosis factor-alpha (TNFalpha) and 5 microM MG132, an inhibitor of proteasome. Polyamines 14-23 caspase 3 Homo sapiens 37-46 15941855-9 2005 The effect of DFMO on TNFalpha/MG132-induced upregulation of caspase-3 activity was reversed by the addition of 100 microM putrescine, confirming that polyamines were really involved in the apoptotic process. Polyamines 151-161 caspase 3 Homo sapiens 61-70 15685629-6 2005 Real time PCR revealed that addition of polyamines to the culture media decreased the ratio of mRNA expression of Bak/Bcl-xL, Fas/Bcl-xL, and caspase 3, and enhanced mRNA expression of ornithine decarboxylase (ODC) and spermidine synthase, enzymes of polyamine biosynthesis. Polyamines 40-50 caspase 3 Homo sapiens 142-151 15994315-10 2005 These results indicate that polyamines regulate PP2A activity, and inhibition of PP2A in response to polyamine depletion increases steady state levels of Bad and Bcl-2 proteins and their phosphorylation and thereby prevents cytochrome c release, caspase-9, and caspase-3 activation. Polyamines 28-38 caspase 3 Homo sapiens 261-270 15994315-10 2005 These results indicate that polyamines regulate PP2A activity, and inhibition of PP2A in response to polyamine depletion increases steady state levels of Bad and Bcl-2 proteins and their phosphorylation and thereby prevents cytochrome c release, caspase-9, and caspase-3 activation. Polyamines 28-37 caspase 3 Homo sapiens 261-270 15685629-6 2005 Real time PCR revealed that addition of polyamines to the culture media decreased the ratio of mRNA expression of Bak/Bcl-xL, Fas/Bcl-xL, and caspase 3, and enhanced mRNA expression of ornithine decarboxylase (ODC) and spermidine synthase, enzymes of polyamine biosynthesis. Polyamines 40-49 caspase 3 Homo sapiens 142-151 15024023-0 2004 Akt kinase activation blocks apoptosis in intestinal epithelial cells by inhibiting caspase-3 after polyamine depletion. Polyamines 100-109 caspase 3 Homo sapiens 84-93 15024023-9 2004 These results indicate that polyamine depletion induces the Akt activation mediating suppression of apoptosis via inhibition of caspase-3 in normal intestinal epithelial cells. Polyamines 28-37 caspase 3 Homo sapiens 128-137 15106734-5 2004 Increase of Fas/Apo-1 expression and caspase-8 and caspase-3 activation focused two typical steps in the pathway of the pro-apoptotic mechanism exhibited by polyamines, even if to a different extent: spermine > spermidine > putrescine. Polyamines 157-167 caspase 3 Homo sapiens 51-60 11978014-8 2002 Depletion of polyamines induced activation of caspase-3 and disruption of the mitochondrial membrane potential (Delta psi m). Polyamines 13-23 caspase 3 Homo sapiens 46-55 9661878-1 1998 The polyamine analogue, N1-ethyl-N11-[(cycloheptyl)methyl]-4,8-diazaundecane (CHENSpm)-induced programmed cell death in NCI H157 cells is accompanied by cytochrome c release, the loss of mitochondrial membrane potential, activation of caspase-3, caspase-mediated poly(ADP-ribose) polymerase cleavage, G2-M arrest, and DNA and nuclear fragmentation. Polyamines 4-13 caspase 3 Homo sapiens 235-244 11698350-0 2001 Activation of caspase-3 activity and apoptosis in MDA-MB-468 cells by N(omega)-hydroxy-L-arginine, an inhibitor of arginase, is not solely dependent on reduction in intracellular polyamines. Polyamines 179-189 caspase 3 Homo sapiens 14-23 11698350-2 2001 These actions of NOHA were abolished in the presence of exogenous L-ornithine suggesting that a reduction in the intracellular polyamine content might be responsible for the activation of caspase-3 and apoptotic actions of NOHA. Polyamines 127-136 caspase 3 Homo sapiens 188-197 11698350-7 2001 Our results, therefore, indicate that the activation of caspase-3 and apoptosis observed with NOHA cannot be solely explained by a reduction in intracellular polyamine levels and that other mechanisms need to be also considered. Polyamines 158-167 caspase 3 Homo sapiens 56-65