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Utilize este identificador para citar ou criar um link para este item: http://acervodigital.unesp.br/handle/11449/111203
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dc.contributor.authorSilva, Sabrina Daniela da-
dc.contributor.authorAlaoui-Jamali, Moulay A.-
dc.contributor.authorSoares, Fernando Augusto-
dc.contributor.authorCarraro, Dirce Maria-
dc.contributor.authorBrentani, Helena Paula-
dc.contributor.authorHier, Michael-
dc.contributor.authorRogatto, Silvia Regina-
dc.contributor.authorKowalski, Luiz Paulo-
dc.date.accessioned2014-12-03T13:07:03Z-
dc.date.accessioned2016-10-25T19:48:11Z-
dc.date.available2014-12-03T13:07:03Z-
dc.date.available2016-10-25T19:48:11Z-
dc.date.issued2014-02-01-
dc.identifierhttp://dx.doi.org/10.1002/cncr.28404-
dc.identifier.citationCancer. Hoboken: Wiley-blackwell, v. 120, n. 3, p. 352-362, 2014.-
dc.identifier.issn0008-543X-
dc.identifier.urihttp://hdl.handle.net/11449/111203-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/111203-
dc.description.abstractBACKGROUND: Locoregional recurrence and distant metastases are ominous events in patients with advanced oral squamous cell carcinoma (OSCC). The objective of this study was to identify functional biomarkers that are predictive of OSCC progression to metastasis.METHODSThe expression profile of a network of epithelial-mesenchymal transition (EMT) genes was investigated in a large cohort of patients with progressive OSCC using a complimentary DNA microarray platform coupled to quantitative reverse transcriptase-polymerase chain reaction and immunohistochemical analyses. Therapeutic potential was investigated in vitro and in vivo using an orthotopic mouse model of metastatic OSCC growing in the tongue microenvironment.RESULTSAmong deregulated EMT genes, the Twist-related protein 1 (TWIST1) transcription factor and several of its regulated genes were significantly overexpressed across advanced stages of OSCC. This result was corroborated by the clinical observation that Twist1 up-regulation predicted the occurrence of lymph node and lung metastases as well as poor patient survival. In support of Twist1 as a driver of OSCC progression, the up-regulation of Twist1 was observed in cells isolated from patients with metastatic OSCC. The inhibition of Twist1 in these metastatic cells induced a potent inhibition of cell invasiveness in vitro as well as progression in vivo.CONCLUSIONSThe current results provide evidence for the prognostic value and therapeutic potential of a network of Twist genes in patients with advanced OSCC. Cancer 2014;120:352-362. (c) 2013 American Cancer Society.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipCanadian Institutes for Health Research (CIHR)-
dc.description.sponsorshipCanadian Cancer Society-
dc.description.sponsorshipQuebec Breast Cancer Foundation-
dc.format.extent352-362-
dc.language.isoeng-
dc.publisherWiley-Blackwell-
dc.sourceWeb of Science-
dc.subjectoral squamous cell carcinomaen
dc.subjectepithelial-mesenchymal transitionen
dc.subjectTwisten
dc.subjectmetastasisen
dc.subjectclinical outcomeen
dc.titleTWIST1 Is a Molecular Marker for a Poor Prognosis in Oral Cancer and Represents a Potential Therapeutic Targeten
dc.typeoutro-
dc.contributor.institutionAC Camargo Canc Ctr-
dc.contributor.institutionMcGill Univ-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationAC Camargo Canc Ctr, Dept Head & Neck Surg & Otorhinolaryngol, Sao Paulo, Brazil-
dc.description.affiliationMcGill Univ, Jewish Gen Hosp, Lady Davis Inst Med Res, Montreal, PQ H3T 1E2, Canada-
dc.description.affiliationMcGill Univ, Jewish Gen Hosp, Segal Canc Ctr, Montreal, PQ H3T 1E2, Canada-
dc.description.affiliationMcGill Univ, Dept Otolaryngol Head & Neck Surg, Montreal, PQ H3T 1E2, Canada-
dc.description.affiliationUniv Sao Paulo, AC Camargo Canc Ctr, Dept Anat Pathol, Sao Paulo, Brazil-
dc.description.affiliationUniv Sao Paulo, Fac Dent, Sao Paulo, Brazil-
dc.description.affiliationAC Camargo Canc Ctr, Mol Biol Lab, Sao Paulo, Brazil-
dc.description.affiliationAC Camargo Canc Ctr, Biotechnol Lab, Sao Paulo, Brazil-
dc.description.affiliationSao Paulo State Univ, Dept Urol, NeoGene Lab, Sao Paulo, Brazil-
dc.description.affiliationAC Camargo Canc Ctr, Sao Paulo, Brazil-
dc.description.affiliationUnespSao Paulo State Univ, Dept Urol, NeoGene Lab, Sao Paulo, Brazil-
dc.identifier.doi10.1002/cncr.28404-
dc.identifier.wosWOS:000330267700008-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofCancer-
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