PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 11010810-3 2000 Fenretinide induced high levels of caspase-dependent apoptosis accompanied by an increase in free radicals and the release of cytochrome c in the absence of mitochondrial permeability transition. Fenretinide 0-11 cytochrome c, somatic Homo sapiens 126-138 15326375-6 2004 4HPR-induced apoptosis in these cells was associated with stimulation of reactive oxygen species generation, decreased levels of Bcl-2 protein, release of cytochrome c into the cytosol, increased caspase-3 activity, and poly(ADP-ribose) polymerase cleavage. Fenretinide 0-4 cytochrome c, somatic Homo sapiens 155-167 12815470-0 2003 Fenretinide induces cytochrome c release, caspase 9 activation and apoptosis in the absence of mitochondrial membrane depolarisation. Fenretinide 0-11 cytochrome c, somatic Homo sapiens 20-32 15650234-2 2004 Fenretinide-induced cell death of neuroblastoma cells is caspase dependent and results in the release of cytochrome c from mitochondria independently of changes in permeability transition. Fenretinide 0-11 cytochrome c, somatic Homo sapiens 105-117 11010810-7 2000 These results suggest that the effector pathway of fenretinide-induced apoptosis of neuroblastoma is caspase dependent, involving mitochondrial release of cytochrome c independently of permeability changes, and mediated by specific RARs. Fenretinide 51-62 cytochrome c, somatic Homo sapiens 155-167 17216584-1 2007 Fenretinide-induced apoptosis of neuroectodermal tumour cells is mediated through generation of reactive oxygen species (ROS), endoplasmic reticulum (ER) stress, mitochondrial cytochrome c release and caspase activation. Fenretinide 0-11 cytochrome c, somatic Homo sapiens 176-188 18549809-4 2008 4-HPR-induced mitochondrial translocation of Bax, release of mitochondrial cytochrome c, and activation of caspase-3 were markedly attenuated in U373MG cells that stably expressed COX6A1. Fenretinide 0-5 cytochrome c, somatic Homo sapiens 75-87 17700534-5 2008 Furthermore, inhibition of p38(MAPK) activity and knockdown of EWS-Fli1 reduced fenretinide-induced mitochondrial permeabilization, cytochrome c release, caspase and PARP cleavage, consistent with the hypothesis that p38(MAPK) is critical for activation of the death cascade by fenretinide in ESFT cells. Fenretinide 80-91 cytochrome c, somatic Homo sapiens 132-144 10597238-0 1999 Implication of mitochondria-derived reactive oxygen species, cytochrome C and caspase-3 in N-(4-hydroxyphenyl)retinamide-induced apoptosis in cervical carcinoma cells. Fenretinide 91-120 cytochrome c, somatic Homo sapiens 61-73 16407847-5 2006 SP600125, a JNK inhibitor, suppressed 4HPR-induced c-Jun phosphorylation, cytochrome c release from mitochondria and apoptosis. Fenretinide 38-42 cytochrome c, somatic Homo sapiens 74-86