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dc.contributor.authorPértega-Gomes, Nelma-
dc.contributor.authorVízcaíno, Ramón-
dc.contributor.authorGonçalves, Vera M.-
dc.contributor.authorPinheiro, Céline-
dc.contributor.authorSilva, Joana-
dc.contributor.authorPereira, Helena-
dc.contributor.authorMonteiro, Pedro-
dc.contributor.authorHenrique, Rui M.-
dc.contributor.authorReis, R. M.-
dc.contributor.authorLopes, Carlos-
dc.contributor.authorBaltazar, Fátima-
dc.date.accessioned2012-04-18T11:26:39Z-
dc.date.available2012-04-18T11:26:39Z-
dc.date.issued2011-07-
dc.identifier.issn1471-2407por
dc.identifier.urihttps://hdl.handle.net/1822/18731-
dc.description.abstractBACKGROUND. Monocarboxylate transporters (MCTs) are transmembrane proteins involved in the transport of monocarboxylates across the plasma membrane, which appear to play an important role in solid tumours, however the role of MCTs in prostate cancer is largely unknown.The aim of the present work was to evaluate the clinico-pathological value of monocarboxylate transporters (MCTs) expression, namely MCT1, MCT2 and MCT4, together with CD147 and gp70 as MCT1/4 and MCT2 chaperones, respectively, in prostate carcinoma. METHODS. Prostate tissues were obtained from 171 patients, who performed radical prostatectomy and 14 patients who performed cystoprostatectomy. Samples and clinico-pathological data were retrieved and organized into tissue microarray (TMAs) blocks. Protein expression was evaluated by immunohistochemistry in neoplastic (n= 171), adjacent non-neoplastic tissues (n= 135), PIN lesions (n=40) and normal prostatic tissue (n=14). Protein expression was correlated with patients' clinicopathologic characteristics. RESULTS. In the present study, a significant increase of MCT2 and MCT4 expression in the cytoplasm of tumour cells and a significant decrease in both MCT1 and CD147 expression in prostate tumour cells was observed when compared to normal tissue. All MCT isoforms and CD147 were expressed in PIN lesions. Importantly, for MCT2 and MCT4 the expression levels in PIN lesions were between normal and tumour tissue, which might indicate a role for these MCTs in the malignant transformation. Associations were found between MCT1, MCT4 and CD147 expressions and poor prognosis markers; importantly MCT4 and CD147 overexpression correlated with higher PSA levels, Gleason score and pT stage, as well as with perineural invasion and biochemical recurrence. CONCLUSIONS. Our data provides novel evidence for the involvement of MCTs in prostate cancer. According to our results, we consider that MCT2 should be further explored as tumour marker and both MCT4 and CD147 as markers of poor prognosis in prostate cancer.por
dc.description.sponsorshipNPG, CP and VMG received fellowships from the Portuguese Foundation for Science and Technology (FCT), refs. SFRH/BD/61027/2009, SFRH/BPD/69479/ 2010 and SFRH/BI/33503/2008, respectively. This work was supported by the FCT grant ref. PTDC/SAU-FCF/104347/2008, under the scope of Programa Operacional Temático Factores de Competitividade” (COMPETE) of Quadro Comunitário de Apoio III and co-financed by Fundo Comunitário Europeu FEDER.por
dc.language.isoengpor
dc.publisherBioMed Central (BMC)por
dc.rightsopenAccesspor
dc.subjectMonocarboxylate transporterspor
dc.titleMonocarboxylate transporter 4 (MCT4) and CD147 overexpression is associated with poor prognosis in prostate cancerpor
dc.typearticlepor
dc.peerreviewedyespor
sdum.publicationstatuspublishedpor
oaire.citationStartPage1por
oaire.citationEndPage9por
oaire.citationIssue312por
oaire.citationTitleBMC Cancerpor
oaire.citationVolume11por
dc.identifier.doi10.1186/1471-2407-11-312por
dc.identifier.pmid21787388por
dc.subject.wosScience & Technologypor
sdum.journalBMC Cancerpor
Aparece nas coleções:ICVS - Artigos em revistas internacionais / Papers in international journals

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