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dc.contributor.authorBerman, A. E.de
dc.contributor.authorChubukina, A. N.de
dc.contributor.authorKozlova, N. I.de
dc.contributor.authorMorozevich, G. E.de
dc.contributor.authorShtil, A. A.de
dc.date.accessioned2008-06-17T13:46:31Z-
dc.date.available2008-06-17T13:46:31Z-
dc.date.issued2004-10-11de
dc.identifier.issn1611-2156de
dc.identifier.urihttp://hdl.handle.net/2003/25638-
dc.identifier.urihttp://dx.doi.org/10.17877/DE290R-337-
dc.description.abstractThe aim of the study was to investigate the role of integrins in anchorage dependent apoptosis (anoikis) and in vitro invasion of human breast cancer cell line MCF-7 and its multidrug resistant subline MCF-7Dox. Acquisition of MDR was associated with markedly decreased expression of collagen specific a2ß1 and avß3 integrins, laminin specific a3ß1 and a6ß1 receptors and dramatic up-regulation of fibronectin specific a5ß1 integrin. The MDR subline was substantially more resistant to anoikis than their wild type counterparts. Furthermore, MCF-7Dox cells secreted MMP-9 collagenase and invaded Matrigel. We demonstrate for the first time that stimulation of ß1 integrin signaling strongly sensitizes MCF-7 cells to anoikis.en
dc.language.isoende
dc.relation.ispartofseriesEXCLI Journal ; Vol. 3, 2004en
dc.subjectanoikisen
dc.subjectintegrinsen
dc.subjectmultidrug resistanceen
dc.subjecttumor invasionen
dc.subject.ddc610-
dc.titleExpression of Integrins, Anchorage Dependent Apoptosis and Invasiveness of Multidrug Resistant Human Breast Carcinoma Cellsen
dc.typeTextde
dc.type.publicationtypearticlede
dcterms.accessRightsopen access-
eldorado.dnb.zdberstkatid2132560-1-
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