pubmed-article:16152579 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:16152579 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
pubmed-article:16152579 | lifeskim:mentions | umls-concept:C0007137 | lld:lifeskim |
pubmed-article:16152579 | lifeskim:mentions | umls-concept:C0001511 | lld:lifeskim |
pubmed-article:16152579 | lifeskim:mentions | umls-concept:C1705165 | lld:lifeskim |
pubmed-article:16152579 | lifeskim:mentions | umls-concept:C1515877 | lld:lifeskim |
pubmed-article:16152579 | lifeskim:mentions | umls-concept:C1879547 | lld:lifeskim |
pubmed-article:16152579 | lifeskim:mentions | umls-concept:C2700061 | lld:lifeskim |
pubmed-article:16152579 | lifeskim:mentions | umls-concept:C1517945 | lld:lifeskim |
pubmed-article:16152579 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:16152579 | pubmed:dateCreated | 2006-2-1 | lld:pubmed |
pubmed-article:16152579 | pubmed:abstractText | The relationship between loss of intercellular adhesion and the biologic properties of human squamous cell carcinoma is not well understood. We investigated how abrogation of E-cadherin-mediated adhesion influenced the behavior and phenotype of squamous cell carcinoma in 3D human tissues. Cell-cell adhesion was disrupted in early-stage epithelial tumor cells (HaCaT-II-4) through expression of a dominant-negative form of E-cadherin (H-2Kd-Ecad). Three-dimensional human tissue constructs harboring either H-2Kd-Ecad-expressing or control II-4 cells (pBabe, H-2Kd-EcadDeltaC25) were cultured at an air-liquid interface for 8 days and transplanted to nude mice; tumor phenotype was analyzed 2 days and 2 and 4 weeks later. H-2Kd-Ecad-expressing tumors demonstrated a switch to a high-grade aggressive tumor phenotype characterized by poorly differentiated tumor cells that infiltrated throughout the stroma. This high-grade carcinoma revealed elevated cell proliferation in a random pattern, loss of keratin 1 and diffuse deposition of laminin 5 gamma2 chain. When II-4 cell variants were seeded into type I collagen gels as an in vitro assay for cell migration, we found that only E-cadherin-deficient cells detached, migrated as single cells and expressed N-cadherin. Function-blocking studies demonstrated that this migration was matrix metalloproteinase-dependent, as GM-6001 and TIMP-2, but not TIMP-1, could block migration. Gene expression profiles revealed that E-cadherin-deficient II-4 cells demonstrated increased expression of proteases and cell-cell and cell-matrix proteins. These findings showed that loss of E-cadherin-mediated adhesion plays a causal role in the transition from low- to high-grade squamous cell carcinomas and that the absence of E-cadherin is an important prognostic marker in the progression of this disease. | lld:pubmed |
pubmed-article:16152579 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16152579 | pubmed:language | eng | lld:pubmed |
pubmed-article:16152579 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16152579 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:16152579 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16152579 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16152579 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16152579 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16152579 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16152579 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16152579 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16152579 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:16152579 | pubmed:month | Feb | lld:pubmed |
pubmed-article:16152579 | pubmed:issn | 0020-7136 | lld:pubmed |
pubmed-article:16152579 | pubmed:author | pubmed-author:CaoJianJ | lld:pubmed |
pubmed-article:16152579 | pubmed:author | pubmed-author:ZuckerStanley... | lld:pubmed |
pubmed-article:16152579 | pubmed:author | pubmed-author:FusenigNorber... | lld:pubmed |
pubmed-article:16152579 | pubmed:author | pubmed-author:MargulisAlexa... | lld:pubmed |
pubmed-article:16152579 | pubmed:author | pubmed-author:GarlickJonath... | lld:pubmed |
pubmed-article:16152579 | pubmed:author | pubmed-author:ZhangWeitianW | lld:pubmed |
pubmed-article:16152579 | pubmed:author | pubmed-author:Alt-HollandAd... | lld:pubmed |
pubmed-article:16152579 | pubmed:author | pubmed-author:PawagiSujataS | lld:pubmed |
pubmed-article:16152579 | pubmed:author | pubmed-author:PrabhuPadmaja... | lld:pubmed |
pubmed-article:16152579 | pubmed:author | pubmed-author:PfeifferLaure... | lld:pubmed |
pubmed-article:16152579 | pubmed:author | pubmed-author:GarfieldJacqu... | lld:pubmed |
pubmed-article:16152579 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:16152579 | pubmed:day | 15 | lld:pubmed |
pubmed-article:16152579 | pubmed:volume | 118 | lld:pubmed |
pubmed-article:16152579 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:16152579 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:16152579 | pubmed:pagination | 821-31 | lld:pubmed |
pubmed-article:16152579 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
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pubmed-article:16152579 | pubmed:year | 2006 | lld:pubmed |
pubmed-article:16152579 | pubmed:articleTitle | Loss of intercellular adhesion activates a transition from low- to high-grade human squamous cell carcinoma. | lld:pubmed |
pubmed-article:16152579 | pubmed:affiliation | Division of Cancer Biology and Tissue Engineering, Department of Oral and Maxillofacial Pathology, School of Dental Medicine, Tufts University, Boston, MA 02111, USA. | lld:pubmed |
pubmed-article:16152579 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:16152579 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
entrez-gene:999 | entrezgene:pubmed | pubmed-article:16152579 | lld:entrezgene |
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