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Significance of glycolytic metabolism-related protein expression in colorectal cancer, lymph node and hepatic metastasis.

Authors :
Martins, Sandra Fernandes
Amorim, Ricardo
Viana-Pereira, Marta
Pinheiro, Céline
Alves Costa, Ricardo Filipe
Silva, Patrícia
Couto, Carla
Alves, Sara
Fernandes, Sara
Vilaça, Sónia
Falcão, Joaquim
Marques, Herlander
Pardal, Fernando
Rodrigues, Mesquita
Preto, Ana
Reis, Rui Manuel
Longatto-Filho, Adhemar
Baltazar, Fátima
Costa, Ricardo Filipe Alves
Source :
BMC Cancer. 7/26/2016, Vol. 16, p1-15. 15p. 1 Diagram, 10 Charts, 2 Graphs.
Publication Year :
2016

Abstract

<bold>Background: </bold>Colorectal cancer (CRC) is one of the most common malignancies and a leading cause of cancer death worldwide. Most cancer cells display high rates of glycolysis with production of lactic acid, which is then exported to the microenvironment by monocarboxylate transporters (MCTs). The main aim of this study was to evaluate the significance of MCT expression in a comprehensive series of primary CRC cases, lymph node and hepatic metastasis.<bold>Methods: </bold>Expressions of MCT1, MCT4, CD147 and GLUT1 were studied in human samples of CRC, lymph node and hepatic metastasis, by immunohistochemistry.<bold>Results: </bold>All proteins were overexpressed in primary CRC, lymph node and hepatic metastasis, when compared with non-neoplastic tissue, with exception of MCT1 in lymph node and hepatic metastasis. MCT1 and MCT4 expressions were associated with CD147 and GLUT1 in primary CRC. These markers were associated with clinical pathological features, reflecting the putative role of these metabolism-related proteins in the CRC setting.<bold>Conclusion: </bold>These findings provide additional evidence for the pivotal role of MCTs in CRC maintenance and progression, and support the use of MCTs as biomarkers and potential therapeutic targets in primary and metastatic CRC. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14712407
Volume :
16
Database :
Academic Search Index
Journal :
BMC Cancer
Publication Type :
Academic Journal
Accession number :
117068399
Full Text :
https://doi.org/10.1186/s12885-016-2566-9