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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/74420
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dc.contributor.authorMoroz, Andrei-
dc.contributor.authorDelella, Flávia K.-
dc.contributor.authorLacorte, Lívia M.-
dc.contributor.authorDeffune, Elenice-
dc.contributor.authorFelisbino, Sérgio L.-
dc.date.accessioned2014-05-27T11:28:13Z-
dc.date.accessioned2016-10-25T18:42:53Z-
dc.date.available2014-05-27T11:28:13Z-
dc.date.available2016-10-25T18:42:53Z-
dc.date.issued2013-01-25-
dc.identifierhttp://dx.doi.org/10.1016/j.bbrc.2012.12.031-
dc.identifier.citationBiochemical and Biophysical Research Communications, v. 430, n. 4, p. 1319-1321, 2013.-
dc.identifier.issn0006-291X-
dc.identifier.issn1090-2104-
dc.identifier.urihttp://hdl.handle.net/11449/74420-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/74420-
dc.description.abstractHigh-grade prostate cancers express high levels of matrix metalloproteinases (MMPs), major enzymes involved in tumor invasion and metastasis. However, the tumor cell lines commonly employed for prostate cancer research express only small amounts of MMPs when cultivated as monolayer cultures, in common culture media. The present study was conducted to ascertain whether culture conditions that include fibronectin can alter MMP2 and MMP9 expression by the human prostatic epithelial cell lines RWPE-1, LNCaP and PC-3. These cells were individually seeded at 2×104cells/cm2, cultivated until they reached 80% confluence, and then exposed for 4h to fibronectin, after which the conditioned medium was analyzed by gelatin zymography. Untreated cells were given common medium. Only RWPE-1 cells express detectable amounts of MMP9 when cultivated in common medium, whereas the addition of fibronectin induced high expression levels of pro and active forms of MMP2 in all tested cell lines. Our findings demonstrate that normal and tumor prostate cell lines express MMP2 activity when in contact with extracellular matrix components or blood plasma proteins such as fibronectin. Future studies of transcriptomes and proteomes in prostate cancer research using these cell lines should not neglect these important conclusions. © 2012 Elsevier Inc..en
dc.format.extent1319-1321-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectFibronectin-
dc.subjectLNCaP-
dc.subjectMMP2-
dc.subjectMMP9-
dc.subjectPC-3-
dc.subjectRWPE-1-
dc.subjectfibronectin-
dc.subjectgelatin-
dc.subjectgelatinase A-
dc.subjectplasma protein-
dc.subjectcancer cell-
dc.subjectcancer cell culture-
dc.subjectcell strain LNCaP-
dc.subjectcontrolled study-
dc.subjectculture medium-
dc.subjectenzyme activity-
dc.subjectextracellular matrix-
dc.subjecthuman-
dc.subjecthuman cell-
dc.subjectpriority journal-
dc.subjectprostate cancer-
dc.subjectprostate epithelium-
dc.subjectprotein blood level-
dc.subjectprotein expression-
dc.subjectprotein function-
dc.subjectprotein induction-
dc.subjectprotein protein interaction-
dc.subjectzymography-
dc.subjectCell Culture Techniques-
dc.subjectCell Line, Tumor-
dc.subjectFibronectins-
dc.subjectHumans-
dc.subjectMale-
dc.subjectMatrix Metalloproteinase 2-
dc.subjectMatrix Metalloproteinase 9-
dc.subjectProstatic Neoplasms-
dc.titleFibronectin induces MMP2 expression in human prostate cancer cellsen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUniv Estadual Paulista - UNESP Institute of Biosciences Department of Morphology, Botucatu, SP-
dc.description.affiliationUniv Estadual Paulista - UNESP Botucatu Medical School, Blood Transfusion Center, Cell Engineering Lab., Botucatu, SP-
dc.description.affiliationUniv Estadual Paulista - UNESP Botucatu Medical School Department of Urology, Botucatu, SP-
dc.description.affiliationUnespUniv Estadual Paulista - UNESP Institute of Biosciences Department of Morphology, Botucatu, SP-
dc.description.affiliationUnespUniv Estadual Paulista - UNESP Botucatu Medical School, Blood Transfusion Center, Cell Engineering Lab., Botucatu, SP-
dc.description.affiliationUnespUniv Estadual Paulista - UNESP Botucatu Medical School Department of Urology, Botucatu, SP-
dc.identifier.doi10.1016/j.bbrc.2012.12.031-
dc.identifier.wosWOS:000315075200023-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-84872871834.pdf-
dc.relation.ispartofBiochemical and Biophysical Research Communications-
dc.identifier.scopus2-s2.0-84872871834-
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