Source:http://linkedlifedata.com/resource/pubmed/id/20949323
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2011-3-29
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pubmed:abstractText |
Vasopressin-activated calcium-mobilizing (VACM-1) protein is a cul-5 gene product that forms complexes with a subclass of ubiquitin E3 ligases involved in proteasomal protein degradation. The expression of VACM-1 cDNA in the T47D breast cancer cell line inhibits growth and decreases phosphorylation of mitogen activated protein kinase. Factors that regulate expression or stability of VACM-1 protein have not been identified, however. In our search to identify drugs/substances that may control VACM-1 protein expression, we examined the effects of resveratrol (trans-3,5,4'-trihydroxystilbene), a natural component in the human diet which inhibits tumor initiation and promotion. CMV vector and VACM-1 cDNA stably transfected T47D breast cancer-derived cells were treated with resveratrol and cell growth and VACM-1 protein concentrations were measured. Since the cellular mechanism of resveratrol-dependent inhibition of cell growth also involves the regulation of estrogen receptors, the effect of 17-?-estradiol and resveratrol on ER? levels and on cell growth was examined in control and in VACM-1 cDNA transfected cells. Our results demonstrate that antiproliferative effect of resveratrol observed in the control T47D cancer cells was significantly enhanced in VACM-1 cDNA transfected T47D cells. Western blot results indicated that resveratrol increased VACM-1 protein concentration. Finally, treatment with resveratrol for 24 and 48 h attenuated 17-?-estradiol induced increase in cell growth both in control and in VACM-1 cDNA transfected cells. The effect was significantly higher in the VACM-1 cDNA transfected cells when compared to controls. These results indicate that the antiproliferative effect of resveratrol may involve induction of VACM-1/cul5.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/CUL5 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Cullin Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary,
http://linkedlifedata.com/resource/pubmed/chemical/Estradiol,
http://linkedlifedata.com/resource/pubmed/chemical/Estrogen Receptor alpha,
http://linkedlifedata.com/resource/pubmed/chemical/Stilbenes,
http://linkedlifedata.com/resource/pubmed/chemical/resveratrol
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1573-6822
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
27
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
95-105
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pubmed:meshHeading |
pubmed-meshheading:20949323-Cell Line, Tumor,
pubmed-meshheading:20949323-Cell Movement,
pubmed-meshheading:20949323-Cell Nucleus,
pubmed-meshheading:20949323-Cell Proliferation,
pubmed-meshheading:20949323-Cullin Proteins,
pubmed-meshheading:20949323-DNA, Complementary,
pubmed-meshheading:20949323-Dose-Response Relationship, Drug,
pubmed-meshheading:20949323-Estradiol,
pubmed-meshheading:20949323-Estrogen Receptor alpha,
pubmed-meshheading:20949323-Humans,
pubmed-meshheading:20949323-Stilbenes,
pubmed-meshheading:20949323-Transfection
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pubmed:year |
2011
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pubmed:articleTitle |
Resveratrol enhances anti-proliferative effect of VACM-1/cul5 in T47D cancer cells.
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pubmed:affiliation |
Department of Biology, Hope College, Holland, MI 49422-9000, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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