Source:http://linkedlifedata.com/resource/pubmed/id/20696234
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2010-9-29
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pubmed:abstractText |
The pro-apoptotic activity of J-7, a synthetic methyl jasmonate derivative, on the Hep3B human hepatocarcinoma cell line was investigated. Treatment of Hep3B cells with J-7 resulted in growth inhibition and the induction of apoptosis as measured by trypan blue-excluding cells, MTT assay, nuclear staining, DNA fragmentation, and flow cytometry analysis. The increased apoptotic events in Hep3B cells caused by J-7 were associated with the alteration in the ratio of Bax/Bcl-2 protein expression. J-7 treatment induced the expression of death receptor-related proteins such as death receptor 5, which triggered the activation of caspase-8 and the down-regulation of the whole Bid expression. In addition, the apoptosis induction by J-7 was correlated with the activation of caspase-9 and caspase-3, down-regulation IAP family proteins such as XIAP and cIAP-1, and concomitant degradation of poly (ADP-ribose) polymerase. However, the cytotoxic and apoptotic effects induced by J-7 were significantly inhibited by z-DEVD-fmk, a caspase-3 inhibitor, which demonstrates the important role that caspase-3 plays in the process. Furthermore, blocking the extracellular signal-regulated protein kinase and c-Jun N-terminal kinase pathways showed increased apoptosis and the activation of caspases in J-7-induced apoptosis. The results indicated that J-7 induces the apoptosis of Hep3B cells through a signaling cascade of death-receptor-mediated extrinsic as well as mitochondria-mediated intrinsic caspase pathways, which are associated with the activation of the mitogen-activated protein kinases signal pathway.
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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/Antineoplastic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Caspases,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclopentanes,
http://linkedlifedata.com/resource/pubmed/chemical/Fatty Acids, Unsaturated,
http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Death Domain
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1879-3177
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2010 Elsevier Ltd. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
24
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1920-6
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pubmed:meshHeading |
pubmed-meshheading:20696234-Antineoplastic Agents,
pubmed-meshheading:20696234-Apoptosis,
pubmed-meshheading:20696234-Carcinoma, Hepatocellular,
pubmed-meshheading:20696234-Caspases,
pubmed-meshheading:20696234-Cell Line, Tumor,
pubmed-meshheading:20696234-Cyclopentanes,
pubmed-meshheading:20696234-DNA Fragmentation,
pubmed-meshheading:20696234-Fatty Acids, Unsaturated,
pubmed-meshheading:20696234-Flow Cytometry,
pubmed-meshheading:20696234-Humans,
pubmed-meshheading:20696234-Liver Neoplasms,
pubmed-meshheading:20696234-Mitochondria,
pubmed-meshheading:20696234-Mitogen-Activated Protein Kinases,
pubmed-meshheading:20696234-Receptors, Death Domain,
pubmed-meshheading:20696234-Signal Transduction
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pubmed:year |
2010
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pubmed:articleTitle |
A methyl jasmonate derivative, J-7, induces apoptosis in human hepatocarcinoma Hep3B cells in vitro.
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pubmed:affiliation |
Blue-Bio Industry Regional Innovation Center, Dongeui University, Busan 614-714, South Korea.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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