Author(s): Oliveira, Antônio Talvane Torres ; Pinheiro, Céline ; Filho, A. L. ; Brito, Maria José ; Martinho, Olga ; Matos, Delcio ; Carvalho, André Lopes ; Vazquez, Vinícius Lima ; Silva, Thiago Buosi ; Scapulatempo-Neto, Cristovam ; Saad, Sarhan Sydney ; Reis, R. M. ; Baltazar, Fátima
Date: 2012
Persistent ID: https://hdl.handle.net/1822/24224
Origin: RepositóriUM - Universidade do Minho
Subject(s): Monocarboxylate transporters; CD147; Cancer metabolism; GISTs
Monocarboxylate transporters (MCTs) have been described to play an important role in cancer, but to date there are no reports on the significance of MCT expression in gastrointestinal stromal tumors (GISTs). The aim of the present work was to assess the value of MCT expression, as well as co-expression with the MCT chaperone CD147 in GISTs and evaluate their clinical-pathological significance. We analyzed the immunohistochemical expression of MCT1, MCT2, MCT4 and CD147 in a series of 64 GISTs molecularly characterized for KIT, PDGFRA and BRAF mutations. MCT1, MCT2 and MCT4 were highly expressed in GISTs. CD147 expression was associated with mutated KIT (p = 0.039), as well as a progressive increase in Fletcher’s Risk of Malignancy (p = 0.020). Importantly, co-expression of MCT1 with CD147 was associated with low patient’s overall survival (p = 0.037). These findings suggest that co-expression of MCT1 with its chaperone CD147 is involved in GISTs aggressiveness, pointing to a contribution of cancer cell metabolic adaptations in GIST development and/or progression.
