Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:16152579rdf:typepubmed:Citationlld:pubmed
pubmed-article:16152579lifeskim:mentionsumls-concept:C0086418lld:lifeskim
pubmed-article:16152579lifeskim:mentionsumls-concept:C0007137lld:lifeskim
pubmed-article:16152579lifeskim:mentionsumls-concept:C0001511lld:lifeskim
pubmed-article:16152579lifeskim:mentionsumls-concept:C1705165lld:lifeskim
pubmed-article:16152579lifeskim:mentionsumls-concept:C1515877lld:lifeskim
pubmed-article:16152579lifeskim:mentionsumls-concept:C1879547lld:lifeskim
pubmed-article:16152579lifeskim:mentionsumls-concept:C2700061lld:lifeskim
pubmed-article:16152579lifeskim:mentionsumls-concept:C1517945lld:lifeskim
pubmed-article:16152579pubmed:issue4lld:pubmed
pubmed-article:16152579pubmed:dateCreated2006-2-1lld:pubmed
pubmed-article:16152579pubmed:abstractTextThe 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:16152579pubmed:granthttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16152579pubmed:languageenglld:pubmed
pubmed-article:16152579pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16152579pubmed:citationSubsetIMlld:pubmed
pubmed-article:16152579pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16152579pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16152579pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16152579pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16152579pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16152579pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16152579pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16152579pubmed:statusMEDLINElld:pubmed
pubmed-article:16152579pubmed:monthFeblld:pubmed
pubmed-article:16152579pubmed:issn0020-7136lld:pubmed
pubmed-article:16152579pubmed:authorpubmed-author:CaoJianJlld:pubmed
pubmed-article:16152579pubmed:authorpubmed-author:ZuckerStanley...lld:pubmed
pubmed-article:16152579pubmed:authorpubmed-author:FusenigNorber...lld:pubmed
pubmed-article:16152579pubmed:authorpubmed-author:MargulisAlexa...lld:pubmed
pubmed-article:16152579pubmed:authorpubmed-author:GarlickJonath...lld:pubmed
pubmed-article:16152579pubmed:authorpubmed-author:ZhangWeitianWlld:pubmed
pubmed-article:16152579pubmed:authorpubmed-author:Alt-HollandAd...lld:pubmed
pubmed-article:16152579pubmed:authorpubmed-author:PawagiSujataSlld:pubmed
pubmed-article:16152579pubmed:authorpubmed-author:PrabhuPadmaja...lld:pubmed
pubmed-article:16152579pubmed:authorpubmed-author:PfeifferLaure...lld:pubmed
pubmed-article:16152579pubmed:authorpubmed-author:GarfieldJacqu...lld:pubmed
pubmed-article:16152579pubmed:issnTypePrintlld:pubmed
pubmed-article:16152579pubmed:day15lld:pubmed
pubmed-article:16152579pubmed:volume118lld:pubmed
pubmed-article:16152579pubmed:ownerNLMlld:pubmed
pubmed-article:16152579pubmed:authorsCompleteYlld:pubmed
pubmed-article:16152579pubmed:pagination821-31lld:pubmed
pubmed-article:16152579pubmed:dateRevised2007-11-14lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:meshHeadingpubmed-meshheading:16152579...lld:pubmed
pubmed-article:16152579pubmed:year2006lld:pubmed
pubmed-article:16152579pubmed:articleTitleLoss of intercellular adhesion activates a transition from low- to high-grade human squamous cell carcinoma.lld:pubmed
pubmed-article:16152579pubmed:affiliationDivision 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:16152579pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16152579pubmed:publicationTypeResearch Support, N.I.H., Extramurallld:pubmed
entrez-gene:999entrezgene:pubmedpubmed-article:16152579lld:entrezgene
http://linkedlifedata.com/r...entrezgene:pubmedpubmed-article:16152579lld:entrezgene
lhgdn:association:59560lhgdn:found_inpubmed-article:16152579lld:lhgdn
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:16152579lld:pubmed