| pubmed-article:20015385 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:20015385 | lifeskim:mentions | umls-concept:C0206687 | lld:lifeskim |
| pubmed-article:20015385 | lifeskim:mentions | umls-concept:C0227843 | lld:lifeskim |
| pubmed-article:20015385 | lifeskim:mentions | umls-concept:C1707937 | lld:lifeskim |
| pubmed-article:20015385 | lifeskim:mentions | umls-concept:C0205217 | lld:lifeskim |
| pubmed-article:20015385 | lifeskim:mentions | umls-concept:C0599883 | lld:lifeskim |
| pubmed-article:20015385 | lifeskim:mentions | umls-concept:C0205179 | lld:lifeskim |
| pubmed-article:20015385 | pubmed:dateCreated | 2010-1-25 | lld:pubmed |
| pubmed-article:20015385 | pubmed:abstractText | It has been recognized cancer cells acquire characters reminiscent of those of normal stem cells, and the degree of stem cell gene expression correlates with patient prognosis. Lgr5(+) or CD133(+) epithelial stem cells (EpiSCs) have recently been identified and these cells are susceptible to neoplastic transformation. It is unclear, however, whether genes enriched in EpiSCs also contribute in tumor malignancy. Endometrial endometrioid carcinoma (EEC) is a dominant type of the endometrial cancers and is still among the most common female cancers. Clinically endometrial carcinoma is classified into 4 FIGO stages by the degree of tumor invasion and metastasis, and the survival rate is low in patients with higher stages of tumors. Identifying genes shared between advanced tumors and stem cells will not only unmask the mechanisms of tumor malignancy but also provide novel therapeutic targets. | lld:pubmed |
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| pubmed-article:20015385 | pubmed:language | eng | lld:pubmed |
| pubmed-article:20015385 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20015385 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:20015385 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:20015385 | pubmed:issn | 1471-2164 | lld:pubmed |
| pubmed-article:20015385 | pubmed:author | pubmed-author:WangHsei-WeiH... | lld:pubmed |
| pubmed-article:20015385 | pubmed:author | pubmed-author:TsaiChan-YenC... | lld:pubmed |
| pubmed-article:20015385 | pubmed:author | pubmed-author:ChangMargaret... | lld:pubmed |
| pubmed-article:20015385 | pubmed:author | pubmed-author:WangTao-Yeuan... | lld:pubmed |
| pubmed-article:20015385 | pubmed:author | pubmed-author:ChangShing-Jy... | lld:pubmed |
| pubmed-article:20015385 | pubmed:author | pubmed-author:HuTzu-FangTF | lld:pubmed |
| pubmed-article:20015385 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:20015385 | pubmed:volume | 10 | lld:pubmed |
| pubmed-article:20015385 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:20015385 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:20015385 | pubmed:pagination | 613 | lld:pubmed |
| pubmed-article:20015385 | pubmed:dateRevised | 2010-9-27 | lld:pubmed |
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