Source:http://linkedlifedata.com/resource/pubmed/id/18829541
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
19
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pubmed:dateCreated |
2008-10-2
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pubmed:abstractText |
Beclin 1 is an essential mediator of autophagy and a regulator of cell growth and cell death. We examined the effect of Beclin 1 overexpression on the action of estradiol (E(2)) and two antiestrogens, raloxifene and 4-hydroxytamoxifen, in estrogen receptor alpha (ERalpha)-positive MCF-7 breast cancer cells. [(3)H]-thymidine incorporation studies showed that Beclin 1-overexpressing cells (MCF-7 x beclin) had a lower proliferative response to E(2) compared with cells transfected with vector control (MCF-7 x control). There was only a 35% increase in [(3)H]-thymidine incorporation, after 24 hours of E(2) treatment of MCF-7 x beclin cells compared with untreated cells, whereas this increase was 2-fold for MCF-7 x control cells. E(2)-induced changes in the expression of early-response genes were examined by real-time quantitiative PCR. There were significant differences in the pattern of expression of E(2)-induced genes c-myc, c-fos, Erg-1, and Nur77 between MCF-7 x beclin and MCF-7 x control cells two hours after treatment. Although E(2)-induced growth of MCF-7 x control cells was completely inhibited by 500 nmol/L raloxifene or 500 nmol/L 4-hydroxytamoxifen, these concentrations of antiestrogens had no significant effect on the growth of MCF-7 x beclin cells. Confocal microscopic and coimmunoprecipitation studies showed evidence for colocalization and association of Beclin 1 and ERalpha. In addition, E(2) caused a decrease in Akt phosphorylation in MCF-7 x beclin cells, compared with a 3-fold increase in MCF-7 cells, five minutes after treatment. These results indicate that Beclin 1 can down-regulate estrogenic signaling and growth response, and contribute to the development of antiestrogen resistance. This observation might be useful to define and overcome antiestrogen resistance of breast cancer.
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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/Apoptosis Regulatory Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/BECN1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Estradiol,
http://linkedlifedata.com/resource/pubmed/chemical/Estrogen Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Estrogen Receptor alpha,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Raloxifene
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1538-7445
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
1
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pubmed:volume |
68
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
7855-63
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pubmed:meshHeading |
pubmed-meshheading:18829541-Apoptosis Regulatory Proteins,
pubmed-meshheading:18829541-Breast Neoplasms,
pubmed-meshheading:18829541-Cell Proliferation,
pubmed-meshheading:18829541-Down-Regulation,
pubmed-meshheading:18829541-Drug Resistance, Neoplasm,
pubmed-meshheading:18829541-Estradiol,
pubmed-meshheading:18829541-Estrogen Antagonists,
pubmed-meshheading:18829541-Estrogen Receptor alpha,
pubmed-meshheading:18829541-Gene Expression Regulation, Neoplastic,
pubmed-meshheading:18829541-Humans,
pubmed-meshheading:18829541-Membrane Proteins,
pubmed-meshheading:18829541-Raloxifene,
pubmed-meshheading:18829541-Signal Transduction,
pubmed-meshheading:18829541-Tissue Distribution,
pubmed-meshheading:18829541-Tumor Cells, Cultured
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pubmed:year |
2008
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pubmed:articleTitle |
Regulation of estrogenic effects by beclin 1 in breast cancer cells.
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pubmed:affiliation |
Departments of Medicine, Environmental and Occupational Medicine, University of Medicine and Dentistry, New Jersey-Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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