Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1999-4-19
pubmed:abstractText
We have previously shown that treatment by anticancer drugs sensitized tumor cells to Fas (APO-1/CD95)-mediated cell death. The present study demonstrates that the cytotoxic drugs cisplatin, doxorubicin and mitomycin C induce the accumulation of the Fas receptor, the FADD adaptor molecule, the procaspases-8, -3 and -2L and the proapoptotic molecule Bax in several human colon cancer cells. This upregulation is also observed in U3A myeloblastoma cells that do not express STAT-1, a transcription factor involved in the constitutive expression of procaspases. We conclude that anticancer drugs sensitize tumor cells to Fas-mediated cell death by a STAT-1-independent upregulation of molecules involved in this apoptotic pathway.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Adaptor Proteins, Signal Transducing, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD95, http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents, http://linkedlifedata.com/resource/pubmed/chemical/BAX protein, human, http://linkedlifedata.com/resource/pubmed/chemical/CASP3 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/CASP8 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/CASP9 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Caspase 2, http://linkedlifedata.com/resource/pubmed/chemical/Caspase 3, http://linkedlifedata.com/resource/pubmed/chemical/Caspase 8, http://linkedlifedata.com/resource/pubmed/chemical/Caspase 9, http://linkedlifedata.com/resource/pubmed/chemical/Caspases, http://linkedlifedata.com/resource/pubmed/chemical/Cisplatin, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Dactinomycin, http://linkedlifedata.com/resource/pubmed/chemical/Doxorubicin, http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Precursors, http://linkedlifedata.com/resource/pubmed/chemical/FADD protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Fas-Associated Death Domain Protein, http://linkedlifedata.com/resource/pubmed/chemical/Isoenzymes, http://linkedlifedata.com/resource/pubmed/chemical/Mitomycin, http://linkedlifedata.com/resource/pubmed/chemical/Poly(ADP-ribose) Polymerases, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-bcl-2, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Tumor Necrosis Factor, http://linkedlifedata.com/resource/pubmed/chemical/STAT1 Transcription Factor, http://linkedlifedata.com/resource/pubmed/chemical/STAT1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators, http://linkedlifedata.com/resource/pubmed/chemical/bcl-2-Associated X Protein
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0006-291X
pubmed:author
pubmed:copyrightInfo
Copyright 1999 Academic Press.
pubmed:issnType
Print
pubmed:day
24
pubmed:volume
256
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
603-7
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:10080945-Adaptor Proteins, Signal Transducing, pubmed-meshheading:10080945-Antigens, CD95, pubmed-meshheading:10080945-Antineoplastic Agents, pubmed-meshheading:10080945-Apoptosis, pubmed-meshheading:10080945-Carrier Proteins, pubmed-meshheading:10080945-Caspase 2, pubmed-meshheading:10080945-Caspase 3, pubmed-meshheading:10080945-Caspase 8, pubmed-meshheading:10080945-Caspase 9, pubmed-meshheading:10080945-Caspases, pubmed-meshheading:10080945-Cisplatin, pubmed-meshheading:10080945-Colonic Neoplasms, pubmed-meshheading:10080945-DNA-Binding Proteins, pubmed-meshheading:10080945-Dactinomycin, pubmed-meshheading:10080945-Doxorubicin, pubmed-meshheading:10080945-Enzyme Precursors, pubmed-meshheading:10080945-Fas-Associated Death Domain Protein, pubmed-meshheading:10080945-Gene Expression Regulation, Neoplastic, pubmed-meshheading:10080945-Humans, pubmed-meshheading:10080945-Isoenzymes, pubmed-meshheading:10080945-Mitomycin, pubmed-meshheading:10080945-Poly(ADP-ribose) Polymerases, pubmed-meshheading:10080945-Proto-Oncogene Proteins, pubmed-meshheading:10080945-Proto-Oncogene Proteins c-bcl-2, pubmed-meshheading:10080945-RNA, Messenger, pubmed-meshheading:10080945-Receptors, Tumor Necrosis Factor, pubmed-meshheading:10080945-STAT1 Transcription Factor, pubmed-meshheading:10080945-Trans-Activators, pubmed-meshheading:10080945-Transcription, Genetic, pubmed-meshheading:10080945-Tumor Cells, Cultured, pubmed-meshheading:10080945-Up-Regulation, pubmed-meshheading:10080945-bcl-2-Associated X Protein
pubmed:year
1999
pubmed:articleTitle
STAT-1-independent upregulation of FADD and procaspase-3 and -8 in cancer cells treated with cytotoxic drugs.
pubmed:affiliation
Department of Biology and Therapy of Cancer (JE 515), Faculty of Medicine and Pharmacy, 7 boulevard Jeanne d'Arc, Dijon Cédex, 21033, France.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't