Source:http://linkedlifedata.com/resource/pubmed/id/10698352
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2000-3-16
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pubmed:abstractText |
Resveratrol, natural compound found in grapes and wine, has been reported to have a variety of health benefit properties. Based on the structural similarity to the synthetic estrogen diethylstilbestrol, we investigated estrogenic/antiestrogenic effects on human breast cancer cell lines, MCF-7 and MVLN, and scavenging properties using DPPH of both (E)- and (Z)-isomers. Both isomers increased the in vitro growth of MCF-7 cell lines at medium concentrations (10 and 25 microM) whereas the low concentrations (0.1 and 1 microM) had no effect and the high concentration (50 microM) decreased the cell growth and was cytotoxic. The 25 microM (E)-isomer alone was able to reduced the proliferation induced by the estradiol. Low concentrations of (E)- and (Z)-resveratrol (0.1 and 1 microM) and medium concentration 10 microM (Z)-resveratrol did not interfere with the estrogen receptor. In contrast, medium concentrations of (E)-resveratrol (10 and 25 microM) and (Z)-resveratrol (25 microM) functioned as superagonists of estradiol. Whatever the model used, MCF-7 or MVLN cell lines, (Z)-resveratrol was less effective than (E)-resveratrol. Extinction of DPPH and Fe(III) reduction experiments showed that both isomers of resveratrol could act as free radicals scavengers or pro-oxidant compounds. The properties of low concentrations of resveratrol raise the possibility that structure-function studies could lead to the development of more selective estrogen receptor agonists and antagonists, which could be useful as a therapeutic agent.
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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/Estradiol Congeners,
http://linkedlifedata.com/resource/pubmed/chemical/Estrogen Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Free Radical Scavengers,
http://linkedlifedata.com/resource/pubmed/chemical/Iron,
http://linkedlifedata.com/resource/pubmed/chemical/Luciferases,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Estrogen,
http://linkedlifedata.com/resource/pubmed/chemical/Stilbenes,
http://linkedlifedata.com/resource/pubmed/chemical/Vitellogenins,
http://linkedlifedata.com/resource/pubmed/chemical/resveratrol
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0024-3205
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
21
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pubmed:volume |
66
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
769-77
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10698352-Cell Division,
pubmed-meshheading:10698352-Computer Simulation,
pubmed-meshheading:10698352-Estradiol Congeners,
pubmed-meshheading:10698352-Estrogen Antagonists,
pubmed-meshheading:10698352-Free Radical Scavengers,
pubmed-meshheading:10698352-Genes, Reporter,
pubmed-meshheading:10698352-Humans,
pubmed-meshheading:10698352-Iron,
pubmed-meshheading:10698352-Luciferases,
pubmed-meshheading:10698352-Oxidation-Reduction,
pubmed-meshheading:10698352-Receptors, Estrogen,
pubmed-meshheading:10698352-Stereoisomerism,
pubmed-meshheading:10698352-Stilbenes,
pubmed-meshheading:10698352-Tumor Cells, Cultured,
pubmed-meshheading:10698352-Vitellogenins
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pubmed:year |
2000
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pubmed:articleTitle |
Estrogenic/antiestrogenic and scavenging properties of (E)- and (Z)-resveratrol.
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pubmed:affiliation |
UPRES EA 1085 Biomolécules et cibles cellulaires tumorales, UFR de Pharmacie, Limoges, France. basly@unilim.fr
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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