Source:http://linkedlifedata.com/resource/pubmed/id/19305383
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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0006141,
umls-concept:C0007634,
umls-concept:C0013081,
umls-concept:C0017262,
umls-concept:C0033684,
umls-concept:C0034804,
umls-concept:C0086418,
umls-concept:C0185117,
umls-concept:C0205183,
umls-concept:C0205307,
umls-concept:C0678222,
umls-concept:C0699493,
umls-concept:C1554184,
umls-concept:C2911684
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pubmed:issue |
6
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pubmed:dateCreated |
2009-6-4
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pubmed:abstractText |
The hormonal carcinogenesis of breast cancer involves hormone-driven cell proliferation and genetic alterations, including oncogene activation and suppressor gene inactivation. However, the predominant genes involved in these processes are currently unknown. Our previous studies identified a gene, namely alpha-tocopherol-associated protein, which is preferentially expressed in normal/benign breast and prostate tissue, but its expression is downregulated in breast and prostate carcinomas. To further examine its function in hormone-induced carcinogenesis, we examined if there is an association between alpha-tocopherol-associated protein and estrogen-receptor expression in normal/benign breast tissue and in human breast carcinomas. We found that alpha-tocopherol-associated protein is coexpressed with estrogen receptor in the luminal cells of normal/benign breast tissue in a scattered manner by immunohistochemical staining of consecutive tissue sections of 20 cases, whereas alpha-tocopherol-associated protein expression is downregulated in 46% (45 of 98) of estrogen-receptor/progesterone-receptor-positive, so-called luminal type A or B human breast carcinoma. This is similar to the association of alpha-tocopherol-associated protein and androgen receptor expression in normal/benign prostate and prostate carcinomas. In contrast,alpha-tocopherol-associated protein expression is mostly negative in basal, Her2 and triple-negative nonbasal subtypes of high-grade breast carcinomas. These findings are consistent with alpha-tocopherol-associated protein acting as an antiproliferative factor in estrogen-receptor-positive luminal cells in normal/benign breast tissue. alpha-Tocopherol-associated protein downregulation may have triggered hormonal carcinogenesis in at least some of the breast carcinomas, providing further, albeit indirect evidence to support a role for vitamin E in breast cancer prevention.
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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/Carrier Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Lipoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Estrogen,
http://linkedlifedata.com/resource/pubmed/chemical/SEC14L2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Markers, Biological
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1530-0285
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
22
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
770-5
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pubmed:meshHeading |
pubmed-meshheading:19305383-Breast Neoplasms,
pubmed-meshheading:19305383-Carcinoma,
pubmed-meshheading:19305383-Carrier Proteins,
pubmed-meshheading:19305383-Down-Regulation,
pubmed-meshheading:19305383-Female,
pubmed-meshheading:19305383-Gene Expression,
pubmed-meshheading:19305383-Humans,
pubmed-meshheading:19305383-Immunohistochemistry,
pubmed-meshheading:19305383-Lipoproteins,
pubmed-meshheading:19305383-Receptors, Estrogen,
pubmed-meshheading:19305383-Trans-Activators,
pubmed-meshheading:19305383-Tumor Markers, Biological
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pubmed:year |
2009
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pubmed:articleTitle |
Dual expression of alpha-tocopherol-associated protein and estrogen receptor in normal/benign human breast luminal cells and the downregulation of alpha-tocopherol-associated protein in estrogen-receptor-positive breast carcinomas.
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pubmed:affiliation |
Department of Pathology and Laboratory Medicine, University of Rochester Medical School, Rochester, NY 14642, USA.
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pubmed:publicationType |
Journal Article
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