Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/45095

TitleThe metabolic microenvironment of melanomas: prognostic value of MCT1 and MCT4
Author(s)Pinheiro, Céline
Baltazar, Maria de Fátima Monginho
Longatto Filho, Adhemar
Reis, R. M.
KeywordsCancer
Glycolysis
Melanoma
Monocarboxylate transporters
Warburg effect
Issue date16-Apr-2016
PublisherTaylor & Francis
JournalCell Cycle
Abstract(s)BRAF mutations are known drivers of melanoma development and, recently, were also described as players in the Warburg effect, while this reprogramming of energy metabolism has been identified as a possible strategy for treating melanoma patients. Therefore, the aim of this work was to evaluate the expression and prognostic value of a panel of glycolytic metabolism-related proteins in a series of melanomas. The immunohistochemical expression of MCT1, MCT4, GLUT1, and CAIX was evaluated in 356 patients presenting melanoma and 20 patients presenting benign nevi. Samples included 20 benign nevi, 282 primary melanomas, 117 lymph node and 54 distant metastases samples. BRAF mutation was observed in 29/92 (31.5%) melanoma patients and 17/20 (85%) benign nevi samples. NRAS mutation was observed in 4/36 (11.1%) melanoma patients and 1/19 (5.3%) benign nevi samples. MCT4 and GLUT1 expression was significantly increased in metastatic samples, and MCT1, MCT4 and GLUT1 were significantly associated with poor prognostic variables. Importantly, MCT1 and MCT4 were associated with shorter overall survival. In conclusion, the present study brings new insights on metabolic aspects of melanoma, paving the way for the development of new-targeted therapies.
TypeArticle
URIhttp://hdl.handle.net/1822/45095
DOI10.1080/15384101.2016.1175258
ISSN1538-4101
Publisher versionhttp://www.tandfonline.com/doi/abs/10.1080/15384101.2016.1175258?journalCode=kccy20
Peer-Reviewedyes
AccessOpen access
Appears in Collections:ICVS - Artigos em Revistas Internacionais com Referee

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