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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
10
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pubmed:dateCreated |
2001-10-11
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pubmed:abstractText |
The antitumor effect of T cells is executed either through CD95 or Perforin (PFN)/Granzyme B (GrB) pathways. Induction of apoptosis by either mode requires activation of caspase family members. However, recent studies have suggested that cell death can proceed in the absence of caspase induction and apoptotic events. We investigated the contribution of CD95 and PFN/GrB-mediated cytotoxicity to apoptotic and necrotic mechanisms of cell death in human renal cell carcinoma. Although freshly isolated and cultured tumors expressed CD95 on their surface, they were resistant to CD95-mediated apoptosis. CD95 resistance coincided with decreased levels of FADD protein and diminished caspase-3-like activity. In contrast, we demonstrated that tumor cell death mediated by PFN/GrB can be achieved in the absence of functional caspase activity and is accompanied by a dramatic accumulation of nonapoptotic necrotic cells.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Adaptor Proteins, Signal Transducing,
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD95,
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 8,
http://linkedlifedata.com/resource/pubmed/chemical/Caspase 9,
http://linkedlifedata.com/resource/pubmed/chemical/Caspases,
http://linkedlifedata.com/resource/pubmed/chemical/FADD protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/FASLG protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Fas Ligand Protein,
http://linkedlifedata.com/resource/pubmed/chemical/Fas-Associated Death Domain Protein,
http://linkedlifedata.com/resource/pubmed/chemical/GZMB protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Granzymes,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Perforin,
http://linkedlifedata.com/resource/pubmed/chemical/Pore Forming Cytotoxic Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Serine Endopeptidases
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1078-0432
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3276-81
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:11595725-Adaptor Proteins, Signal Transducing,
pubmed-meshheading:11595725-Antibodies, Monoclonal,
pubmed-meshheading:11595725-Antigens, CD95,
pubmed-meshheading:11595725-Apoptosis,
pubmed-meshheading:11595725-Carcinoma, Renal Cell,
pubmed-meshheading:11595725-Carrier Proteins,
pubmed-meshheading:11595725-Caspase 8,
pubmed-meshheading:11595725-Caspase 9,
pubmed-meshheading:11595725-Caspases,
pubmed-meshheading:11595725-Drug Resistance, Neoplasm,
pubmed-meshheading:11595725-Enzyme Activation,
pubmed-meshheading:11595725-Fas Ligand Protein,
pubmed-meshheading:11595725-Fas-Associated Death Domain Protein,
pubmed-meshheading:11595725-Granzymes,
pubmed-meshheading:11595725-Humans,
pubmed-meshheading:11595725-Jurkat Cells,
pubmed-meshheading:11595725-Membrane Glycoproteins,
pubmed-meshheading:11595725-Necrosis,
pubmed-meshheading:11595725-Perforin,
pubmed-meshheading:11595725-Pore Forming Cytotoxic Proteins,
pubmed-meshheading:11595725-Serine Endopeptidases,
pubmed-meshheading:11595725-T-Lymphocytes, Cytotoxic,
pubmed-meshheading:11595725-Tumor Cells, Cultured
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pubmed:year |
2001
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pubmed:articleTitle |
The T cell death knell: immune-mediated tumor death in renal cell carcinoma.
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pubmed:affiliation |
Department of Immunology, The Cleveland Clinic Foundation, Cleveland, OH 44195, USA. R_Uzzo@fccc.edu
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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