Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/49963

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Campo DCValorIdioma
dc.contributor.authorMartinho, Olgapor
dc.contributor.authorSilva-Oliveira, Renatopor
dc.contributor.authorBarbosa, Ana Margarida Martinspor
dc.contributor.authorGranja, Sara Costapor
dc.contributor.authorMiranda-Gonçalves, Verapor
dc.contributor.authorCardoso-Carneiro, Dianapor
dc.contributor.authorPaula, Flávia E. depor
dc.contributor.authorBaltazar, Fátimapor
dc.contributor.authorLongatto, Adhemarpor
dc.contributor.authorReis, R. M.por
dc.contributor.authoret. al.por
dc.date.accessioned2018-02-01T10:37:50Z-
dc.date.available2018-02-01T10:37:50Z-
dc.date.issued2017-01-24-
dc.identifier.citationMartinho, O., Silva-Oliveira, R., Cury, F. P., Barbosa, A. M., Granja, S., Evangelista, A. F., ... & Zanon, M. (2017). HER family receptors are important theranostic biomarkers for cervical cancer: blocking glucose metabolism enhances the therapeutic effect of HER inhibitors. Theranostics, 7(3), 717por
dc.identifier.issn1838-7640por
dc.identifier.urihttps://hdl.handle.net/1822/49963-
dc.description.abstractPersistent HPV infection alone is not sufficient for cervical cancer development, which requires additional molecular alterations for tumor progression and metastasis ultimately leading to a lethal disease. In this study, we performed a comprehensive analysis of HER family receptor alterations in cervical adenocarcinoma. We detected overexpression of HER protein, mainly HER2, which was an independent prognostic marker for these patients. By using in vitro and in vivo approaches, we provided evidence that HER inhibitors, allitinib and lapatinib, were effective in reducing cervical cancer aggressiveness. Furthermore, combination of these drugs with glucose uptake blockers could overcome the putative HIF1-a-mediated resistance to HER-targeted therapies. Thus, we propose that the use of HER inhibitors in association with glycolysis blockers can be a potentially effective treatment option for HER-positive cervical cancer patients.por
dc.description.sponsorshipFINEP (MCTI/FINEP/MS/SCTIE/DECIT-BIOPLAT (1302/13), Brazil and co-funded by the project “ON.2 SR&TD Integrated Program (NORTE-07-0124-FEDER-000017)” co-funded by Programa Operacional Regional do Norte (ON.2- O Novo Norte), Quadro de Referência Estratégico Nacional (QREN), through Fundo Europeu de Desenvolvimento Regional (FEDER). OM is recipient of a post-doc fellowship (SFRH/BPD/108351/2015) from Fundação para a Ciência e Tecnologia (FCT), Portugal. FC is recipient of a master fellowship (2014/03684-0) from Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP). VMG is recipient from a PhD fellowship (SFRH/BD/51997/2012) from Fundação para a Ciência e Tecnologia (FCT), Portugalpor
dc.language.isoengpor
dc.publisherIvyspring International Publisherpor
dc.rightsopenAccesspor
dc.subjectErbBpor
dc.subjectEGFRpor
dc.subjectHER2por
dc.subjectCervical cancerpor
dc.subjectPrognosispor
dc.subjectTargeted therapypor
dc.subjectErbB, EGFRpor
dc.titleHER Family Receptors are Important Theranostic Biomarkers for Cervical Cancer: Blocking Glucose Metabolism Enhances the Therapeutic Effect of HER Inhibitorspor
dc.typearticlepor
dc.peerreviewedyespor
dc.relation.publisherversionhttp://www.thno.org/v07p0717.htmpor
oaire.citationStartPage717por
oaire.citationEndPage732por
oaire.citationIssue3por
oaire.citationVolume7por
dc.date.updated2018-01-09T17:05:00Z-
dc.identifier.eissn1838-7640-
dc.identifier.doi10.7150/thno.17154por
dc.identifier.pmid28255362por
dc.subject.fosCiências Médicas::Medicina Básicapor
dc.description.publicationversioninfo:eu-repo/semantics/publishedVersionpor
dc.subject.wosScience & Technologypor
sdum.journalTheranosticspor
Aparece nas coleções:ICVS - Artigos em revistas internacionais / Papers in international journals

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