Source:http://linkedlifedata.com/resource/pubmed/id/18297401
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2008-3-25
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pubmed:abstractText |
Vinorelbine is a chemotherapeutic vinca alkaloid clinically prescribed for non-small cell lung cancer and breast cancer. Here we studied the mechanism for vinorelbine-induced apoptosis in a human T-cell lymphoma. Although vinorelbine induces DNA fragmentation that is inhibited by specific peptide inhibitors for caspases-9 and -3 in Jurkat cells, caspase-8 deficiency retards vinorelbine-induced apoptosis. Activation of caspase-8 is also observed in vinorelbine-treated cells, and the activity is diminished when the caspase-3 activity is blocked by a specific peptide inhibitor, Ac-DNLC-CHO. Blocking of the Fas receptor with an antagonistic anti-Fas antibody does not affect vinorelbine-induced DNA fragmentation. These results suggest that vinorelbine-induced apoptosis is enhanced by the activation of caspase-8 via caspase-9-mediated activation of caspase-3, but not through a Fas-triggered signal. Western blotting suggests that vinorelbine cleaves caspase-3, -9 and -8 and reduces the amount of mitochondrial cytochrome c. Caspase-8 deficiency suppresses all of these events. A downstream substrate for caspase-8, Bid, is also cleaved in vinorelbine-treated cells, but the Bid truncation is also observed in caspase-8-deficient Jurkat cells. Importantly, recombinant caspases-3 and -9, as well as caspase-8, directly cleaves recombinant Bid in vitro. These results suggest that caspases-3 and -9 participate in Bid truncation, indicating a new mechanism for vinorelbine-induces apoptosis.
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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/BH3 Interacting Domain Death...,
http://linkedlifedata.com/resource/pubmed/chemical/BID protein, human,
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/Cytochromes c,
http://linkedlifedata.com/resource/pubmed/chemical/Vinblastine,
http://linkedlifedata.com/resource/pubmed/chemical/vinorelbine
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1573-675X
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
13
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
523-30
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pubmed:meshHeading |
pubmed-meshheading:18297401-Apoptosis,
pubmed-meshheading:18297401-BH3 Interacting Domain Death Agonist Protein,
pubmed-meshheading:18297401-Caspase 3,
pubmed-meshheading:18297401-Caspase 8,
pubmed-meshheading:18297401-Caspase 9,
pubmed-meshheading:18297401-Cell Line, Tumor,
pubmed-meshheading:18297401-Cytochromes c,
pubmed-meshheading:18297401-Humans,
pubmed-meshheading:18297401-Jurkat Cells,
pubmed-meshheading:18297401-Lymphoma, T-Cell,
pubmed-meshheading:18297401-Vinblastine
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pubmed:year |
2008
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pubmed:articleTitle |
Bid truncation mediated by caspases-3 and -9 in vinorelbine-induced apoptosis.
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pubmed:affiliation |
Faculty of Science and Engineering, Tokyo University of Science, Yamaguchi, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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