Source:http://linkedlifedata.com/resource/pubmed/id/16792412
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2006-6-23
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pubmed:abstractText |
Three new butanolides, kotomolide A (1), isokotomolide A (2), and kotomolide B (3), and a new secobutanolide, secokotomolide A (4), along with 21 known compounds were isolated from the leaves of Cinnamomum kotoense. Their structures were determined by spectroscopic analyses. Compound 4 was found to induce significant cell death in the human HeLa cell line. Apoptotic-related DNA damage can be positively related to the dose of compound 4. The DNA damage was measured by the percentage of subG1 (24 h after the treatment of compound 4) as determined by cell cycle analysis and TUNEL assay. Treatment with 4 significantly increased intracellular H2O2 and/or peroxide, nitric oxide (NO) at 1, 3, and 24 h. Our results also showed that compound 4 induced (a) noticeable reduction of mitochondrial transmembrane potential (DeltaPsi(m)), (b) activation of caspase 3/7, and (c) up-regulation of the p53 expression. Compound 4-induced DNA damage was found to markedly decrease when the cells were pretreated with an intracellular glutathione supplement (glutathione ethyl ester). These results suggest that an increase of H2O2 and/or peroxide by compound 4 is the initial apoptotic event. The intracellular GSH depletion is a critical event in compound 4-induced apoptosis in HeLa cells.
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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/4-Butyrolactone,
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/CASP3 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/CASP7 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Caspase 3,
http://linkedlifedata.com/resource/pubmed/chemical/Caspase 7,
http://linkedlifedata.com/resource/pubmed/chemical/Caspases,
http://linkedlifedata.com/resource/pubmed/chemical/DNA,
http://linkedlifedata.com/resource/pubmed/chemical/Hydrogen Peroxide,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Suppressor Protein p53
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0163-3864
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
69
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
927-33
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16792412-4-Butyrolactone,
pubmed-meshheading:16792412-Antineoplastic Agents,
pubmed-meshheading:16792412-Apoptosis,
pubmed-meshheading:16792412-Caspase 3,
pubmed-meshheading:16792412-Caspase 7,
pubmed-meshheading:16792412-Caspases,
pubmed-meshheading:16792412-Cinnamomum,
pubmed-meshheading:16792412-DNA,
pubmed-meshheading:16792412-DNA Damage,
pubmed-meshheading:16792412-Flow Cytometry,
pubmed-meshheading:16792412-HeLa Cells,
pubmed-meshheading:16792412-Humans,
pubmed-meshheading:16792412-Hydrogen Peroxide,
pubmed-meshheading:16792412-Molecular Structure,
pubmed-meshheading:16792412-Plant Leaves,
pubmed-meshheading:16792412-Plants, Medicinal,
pubmed-meshheading:16792412-Taiwan,
pubmed-meshheading:16792412-Tumor Suppressor Protein p53
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pubmed:year |
2006
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pubmed:articleTitle |
Chemical and cytotoxic constituents from the leaves of Cinnamomum kotoense.
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pubmed:affiliation |
Graduate Institute of Biopharmaceutics, College of Life Sciences, National Chiayi University, Chiayi 600, Taiwan, Republic of China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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