Source:http://linkedlifedata.com/resource/pubmed/id/19754130
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2009-10-23
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pubmed:abstractText |
Three new butanolides, tenuifolide A (1), isotenuifolide A (2), and tenuifolide B (3), a new secobutanolide, secotenuifolide A (4), and one new sesquiterpenoid, tenuifolin (5), along with 16 known compounds were isolated from the stems of Cinnamomum tenuifolium. Their structures were determined by spectroscopic analyses. Compound 4 was found to induce apoptotic-related DNA damage, increase sub-G1 cells, and inhibit the growth of human prostate cancer cells, DU145. In addition, treatment with 4 significantly increased intracellular H2O2 and/or peroxide. The results show that 4 induced (a) noticeable reduction of mitochondrial transmembrane potential (DeltaPsim); (b) significant increase in the ratio of cytochrome c concentration (cytosol/mitochondria); and (c) subsequent activation of caspase-9/caspase-3. Antiproliferation caused by 4 was found to markedly decrease when pretreated with caspase-9/caspase-3 inhibitor. In ROS scavenging, antioxidant, NADPH oxidase, and NO inhibitor studies, pretreatment of DU145 cells with either DPI, dexamethasone, L-NAME, or mannitol decreased 4-induced intracellular DCF fluorescence of ROS. These results suggest that an increase of H2O2 and/or peroxide by 4 is the initial apoptotic event and 4 has anticancer effects on DU145 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, Phytogenic,
http://linkedlifedata.com/resource/pubmed/chemical/Caspase 3,
http://linkedlifedata.com/resource/pubmed/chemical/Caspase 9,
http://linkedlifedata.com/resource/pubmed/chemical/Cytochromes c,
http://linkedlifedata.com/resource/pubmed/chemical/Hydrogen Peroxide
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1520-6025
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
72
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1816-24
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pubmed:meshHeading |
pubmed-meshheading:19754130-4-Butyrolactone,
pubmed-meshheading:19754130-Antineoplastic Agents, Phytogenic,
pubmed-meshheading:19754130-Apoptosis,
pubmed-meshheading:19754130-Caspase 3,
pubmed-meshheading:19754130-Caspase 9,
pubmed-meshheading:19754130-Cinnamomum,
pubmed-meshheading:19754130-Cytochromes c,
pubmed-meshheading:19754130-Dose-Response Relationship, Drug,
pubmed-meshheading:19754130-Drug Screening Assays, Antitumor,
pubmed-meshheading:19754130-Humans,
pubmed-meshheading:19754130-Hydrogen Peroxide,
pubmed-meshheading:19754130-Male,
pubmed-meshheading:19754130-Plant Stems,
pubmed-meshheading:19754130-Plants, Medicinal,
pubmed-meshheading:19754130-Taiwan
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pubmed:year |
2009
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pubmed:articleTitle |
Cytotoxic compounds from the stems of Cinnamomum tenuifolium.
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pubmed:affiliation |
Department of Parasitology and Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan, Republic of China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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