Na,K-ATPase isozymes in colorectal cancer and liver metastases

The goal of this study was to define Na,K-ATPase α and β subunit isoform expression and isozyme composition in colorectal cancer cells and liver metastases. The α1, α3 and β1 isoforms were the most highly expressed in tumor cells and metastases; in the plasma membrane of non-neoplastic cells and mai...

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Bibliographic Details
Main Authors: Marc eBaker Bechmann, Deborah eRotoli, Manuel eMorales, María del Carmen eMaeso, María del Pino eGarcía, Julio eÁvila, Ali eMobasheri, Pablo eMartin-Vasallo
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-01-01
Series:Frontiers in Physiology
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Online Access:http://journal.frontiersin.org/Journal/10.3389/fphys.2016.00009/full
Description
Summary:The goal of this study was to define Na,K-ATPase α and β subunit isoform expression and isozyme composition in colorectal cancer cells and liver metastases. The α1, α3 and β1 isoforms were the most highly expressed in tumor cells and metastases; in the plasma membrane of non-neoplastic cells and mainly in a cytoplasmic location in tumor cells. α1β1 and α3β1 isozymes found in tumor and metastatic cells exhibit the highest and lowest Na+ affinity respectively and the highest K+ affinity. Mesenchymal cell isozymes possess an intermediate Na+ affinity and a low K+ affinity. In cancer, these ions are likely to favor optimal conditions for the function of nuclear enzymes involved in mitosis, especially a high intra-nuclear K+ concentration. A major and striking finding of this study was that in liver, metastasized CRC cells express the α3β1 isozyme. Thus, the α3β1 isozyme could potentially serve as a novel exploratory biomarker of CRC metastatic cells in liver.
ISSN:1664-042X