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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/17987
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dc.contributor.authorCervigne, Nilva K.-
dc.contributor.authorReis, Patricia P.-
dc.contributor.authorMachado, Jerry-
dc.contributor.authorSadikovic, Bekim-
dc.contributor.authorBradley, Grace-
dc.contributor.authorNaranjo Galloni, Natalie-
dc.contributor.authorPintilie, Melania-
dc.contributor.authorJurisica, Igor-
dc.contributor.authorPerez-Ordonez, Bayardo-
dc.contributor.authorGilbert, Ralph-
dc.contributor.authorGullane, Patrick-
dc.contributor.authorIrish, Jonathan-
dc.contributor.authorKamel-Reid, Suzanne-
dc.date.accessioned2014-05-20T13:50:23Z-
dc.date.accessioned2016-10-25T17:02:30Z-
dc.date.available2014-05-20T13:50:23Z-
dc.date.available2016-10-25T17:02:30Z-
dc.date.issued2009-12-15-
dc.identifierhttp://dx.doi.org/10.1093/hmg/ddp446-
dc.identifier.citationHuman Molecular Genetics. Oxford: Oxford Univ Press, v. 18, n. 24, p. 4818-4829, 2009.-
dc.identifier.issn0964-6906-
dc.identifier.urihttp://hdl.handle.net/11449/17987-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/17987-
dc.description.abstractMicroRNAs (miRs) are non-coding RNA molecules involved in cancer initiation and progression. Deregulated miR expression has been implicated in cancer; however, there are no studies implicating an miR signature associated with progression in oral squamous cell carcinoma (OSCC). Although OSCC may develop from oral leukoplakia, clinical and histological assessments have limited prognostic value in predicting which leukoplakic lesions will progress. Our aim was to quantify miR expression changes in leukoplakia and same-site OSCC and to identify an miR signature associated with progression. We examined miR expression changes in 43 sequential progressive samples from 12 patients and four non-progressive leukoplakias from four different patients, using TaqMan Low Density Arrays. The findings were validated using quantitative RT-PCR in an independent cohort of 52 progressive dysplasias and OSCCs, and five non-progressive dysplasias. Global miR expression profiles distinguished progressive leukoplakia/OSCC from non-progressive leukoplakias/normal tissues. One hundred and nine miRs were highly expressed exclusively in progressive leukoplakia and invasive OSCC. miR-21, miR-181b and miR-345 expressions were consistently increased and associated with increases in lesion severity during progression. Over-expression of miR-21, miR-181b and miR-345 may play an important role in malignant transformation. Our study provides the first evidence of an miR signature potentially useful for identifying leukoplakias at risk of malignant transformation.en
dc.description.sponsorshipGalloway Fund administered through the University Health Network-
dc.description.sponsorshipCancer Research Society (Canada)-
dc.format.extent4818-4829-
dc.language.isoeng-
dc.publisherOxford University Press-
dc.sourceWeb of Science-
dc.titleIdentification of a microRNA signature associated with progression of leukoplakia to oral carcinomaen
dc.typeoutro-
dc.contributor.institutionToronto Gen Hosp-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionHosp Sick Children-
dc.contributor.institutionUniv Toronto-
dc.contributor.institutionHosp Calderon Guardia-
dc.contributor.institutionUniv Hlth Network-
dc.description.affiliationToronto Gen Hosp, Ontario Canc Inst, Univ Hlth Network, Div Appl Mol Oncol, Toronto, on M5G 2C4, Canada-
dc.description.affiliationToronto Gen Hosp, Ontario Canc Inst, Univ Hlth Network, Dept Biostat, Toronto, on M5G 2C4, Canada-
dc.description.affiliationToronto Gen Hosp, Ontario Canc Inst, Univ Hlth Network, Dept Comp Sci, Toronto, on M5G 2C4, Canada-
dc.description.affiliationToronto Gen Hosp, Ontario Canc Inst, Univ Hlth Network, Dept Signaling Biol, Toronto, on M5G 2C4, Canada-
dc.description.affiliationToronto Gen Hosp, Ontario Canc Inst, Univ Hlth Network, Dept Pathol, Toronto, on M5G 2C4, Canada-
dc.description.affiliationSão Paulo State Univ, Biosci Inst, Dept Genet, Botucatu, SP, Brazil-
dc.description.affiliationHosp Sick Children, Dept Pediat Lab Med, Toronto, on M5G 1X8, Canada-
dc.description.affiliationHosp Sick Children, Genet & Genome Biol Program, Toronto, on M5G 1X8, Canada-
dc.description.affiliationUniv Toronto, Fac Dent, Toronto, on M5G 1G6, Canada-
dc.description.affiliationHosp Calderon Guardia, Dept Otolaryngol, San Jose, Costa Rica-
dc.description.affiliationUniv Toronto, Dalla Lana Sch Publ Hlth Sci, Toronto, on M5T 3M7, Canada-
dc.description.affiliationUniv Toronto, Princess Margaret Hosp, Dept Otolaryngol Surg Oncol, Toronto, on M5G 2M9, Canada-
dc.description.affiliationUniv Hlth Network, Toronto, on M5G 2M9, Canada-
dc.description.affiliationUnespSão Paulo State Univ, Biosci Inst, Dept Genet, Botucatu, SP, Brazil-
dc.identifier.doi10.1093/hmg/ddp446-
dc.identifier.wosWOS:000272077200013-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofHuman Molecular Genetics-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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