rdf:type |
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lifeskim:mentions |
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pubmed:issue |
28
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pubmed:dateCreated |
2008-7-8
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pubmed:abstractText |
Targeting TRAIL receptors with either recombinant TRAIL or agonistic DR4- or DR5-specific antibodies has been considered a promising treatment for cancer, particularly due to the preferential apoptotic susceptibility of tumor cells over normal cells to TRAIL. However, the realization that many tumors are unresponsive to TRAIL treatment has stimulated interest in identifying apoptotic agents that when used in combination with TRAIL can sensitize tumor cells to TRAIL-mediated apoptosis. Our studies suggest that various apoptosis defects that block TRAIL-mediated cell death at different points along the apoptotic signaling pathway shift the signaling cascade from default apoptosis toward cytoprotective autophagy. We also obtained evidence that inhibition of such a TRAIL-mediated autophagic response by specific knockdown of autophagic genes initiates an effective mitochondrial apoptotic response that is caspase-8-dependent. Currently, the molecular mechanisms linking disabled autophagy to mitochondrial apoptosis are not known. Our analysis of the molecular mechanisms involved in the shift from protective autophagy to apoptosis in response to TRAIL sheds new light on the negative regulation of apoptosis by the autophagic process and by some of its individual components.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/18375389-10321738,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18375389-10625637,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18375389-10894160,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/18375389-9930856
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies,
http://linkedlifedata.com/resource/pubmed/chemical/CASP8 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Caspase 8,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, TNF-Related...,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Tumor Necrosis Factor,
http://linkedlifedata.com/resource/pubmed/chemical/TNF-Related Apoptosis-Inducing...,
http://linkedlifedata.com/resource/pubmed/chemical/TNFRSF10A protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/TNFSF10 protein, human
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
|
pubmed:issn |
0021-9258
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pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
11
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pubmed:volume |
283
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
19665-77
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:18375389-Antibodies,
pubmed-meshheading:18375389-Apoptosis,
pubmed-meshheading:18375389-Autophagy,
pubmed-meshheading:18375389-Caspase 8,
pubmed-meshheading:18375389-Drug Resistance, Neoplasm,
pubmed-meshheading:18375389-Humans,
pubmed-meshheading:18375389-Jurkat Cells,
pubmed-meshheading:18375389-Mitochondria,
pubmed-meshheading:18375389-Neoplasms,
pubmed-meshheading:18375389-Receptors, TNF-Related Apoptosis-Inducing Ligand,
pubmed-meshheading:18375389-Receptors, Tumor Necrosis Factor,
pubmed-meshheading:18375389-TNF-Related Apoptosis-Inducing Ligand
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pubmed:year |
2008
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pubmed:articleTitle |
Involvement of protective autophagy in TRAIL resistance of apoptosis-defective tumor cells.
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pubmed:affiliation |
Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213, USA.
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