Source:http://linkedlifedata.com/resource/pubmed/id/18316615
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2008-3-4
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pubmed:abstractText |
In our present study, we examined whether nuclear localization of Y-box binding protein-1 (YB-1) is associated with the expression of epidermal growth factor receptors (EGFR), hormone receptors, and other molecules affecting breast cancer prognosis. The expression of nuclear YB-1, clinicopathologic findings, and molecular markers [EGFR, HER2, estrogen receptor (ER)alpha, ER beta, progesterone receptor, chemokine (C-X-C motif) receptor 4 (CXCR4), phosphorylated Akt, and major vault protein/lung resistance protein] were immunohistochemically analyzed. The association of the expression of nuclear YB-1 and the molecular markers was examined in breast cancer cell lines using microarrays, quantitative real-time PCR, and Western blot analyses. Knockdown of YB-1 with siRNA significantly reduced EGFR, HER2, and ER alpha expression in ER alpha-positive, but not ER alpha-negative, breast cancer cell lines. Nuclear YB-1 expression was positively correlated with HER2 (P = 0.0153) and negatively correlated with ER alpha (P = 0.0122) and CXCR4 (P = 0.0166) in human breast cancer clinical specimens but was not correlated with EGFR expression. Nuclear YB-1 expression was an independent prognostic factor for overall (P = 0.0139) and progression-free (P = 0.0280) survival. In conclusion, nuclear YB-1 expression might be essential for the acquisition of malignant characteristics via HER2-Akt-dependent pathways in breast cancer patients. The nuclear localization of YB-1 could be an important therapeutic target against not only multidrug resistance but also tumor growth dependent on HER2 and ER alpha.
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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/ERBB2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Estrogen Receptor alpha,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, erbB-2,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Markers, Biological,
http://linkedlifedata.com/resource/pubmed/chemical/Y-Box-Binding Protein 1
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1538-7445
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pubmed:author |
pubmed-author:BasakiYujiY,
pubmed-author:FujiiTeruhikoT,
pubmed-author:HattoriSatoshiS,
pubmed-author:KageMasayoshiM,
pubmed-author:KawaharaAkihikoA,
pubmed-author:KohnoKimitoshiK,
pubmed-author:KuwanoMichihikoM,
pubmed-author:NakanoKenjiK,
pubmed-author:NakashimaKazutakaK,
pubmed-author:NishioKazutoK,
pubmed-author:OnoMayumiM,
pubmed-author:ShirouzuKazuoK,
pubmed-author:YamanaHideakiH,
pubmed-author:YanagawaTakashiT
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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 |
1504-12
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:18316615-Breast Neoplasms,
pubmed-meshheading:18316615-Cell Line, Tumor,
pubmed-meshheading:18316615-Cell Nucleus,
pubmed-meshheading:18316615-Cytoplasm,
pubmed-meshheading:18316615-Disease-Free Survival,
pubmed-meshheading:18316615-Estrogen Receptor alpha,
pubmed-meshheading:18316615-Gene Expression Regulation, Neoplastic,
pubmed-meshheading:18316615-Humans,
pubmed-meshheading:18316615-Models, Biological,
pubmed-meshheading:18316615-Oligonucleotide Array Sequence Analysis,
pubmed-meshheading:18316615-Prognosis,
pubmed-meshheading:18316615-Receptor, erbB-2,
pubmed-meshheading:18316615-Regression Analysis,
pubmed-meshheading:18316615-Tumor Markers, Biological,
pubmed-meshheading:18316615-Y-Box-Binding Protein 1
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pubmed:year |
2008
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pubmed:articleTitle |
Expression of HER2 and estrogen receptor alpha depends upon nuclear localization of Y-box binding protein-1 in human breast cancers.
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pubmed:affiliation |
Center for Innovative Cancer Therapy of the 21st Century Center of Excellence Program for Medical Science, Department of Surgery, Kurume University School of Medicine, Kurume, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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