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      Voltage-gated sodium channels and cancer: is excitability their primary role?

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          Abstract

          Voltage-gated sodium channels (Na V) are molecular characteristics of excitable cells. Their activation, triggered by membrane depolarization, generates transient sodium currents that initiate action potentials in neurons and muscle cells. Sodium currents were discovered by Hodgkin and Huxley using the voltage clamp technique and reported in their landmark series of papers in 1952. It was only in the 1980's that sodium channel proteins from excitable membranes were molecularly characterized by Catterall and his collaborators. Non-excitable cells can also express Na V channels in physiological conditions as well as in pathological conditions. These Na V channels can sustain biological roles that are not related to the generation of action potentials. Interestingly, it is likely that the abnormal expression of Na V in pathological tissues can reflect the re-expression of a fetal phenotype. This is especially true in epithelial cancer cells for which these channels have been identified and sodium currents recorded, while it was not the case for cells from the cognate normal tissues. In cancers, the functional activity of Na V appeared to be involved in regulating the proliferative, migrative, and invasive properties of cells. This review is aimed at addressing the non-excitable roles of Na V channels with a specific emphasis in the regulation of cancer cell biology.

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          SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome.

          Long QT syndrome (LQT) is an inherited disorder that causes sudden death from cardiac arrhythmias, specifically torsade de pointes and ventricular fibrillation. We previously mapped three LQT loci: LQT1 on chromosome 11p15.5, LQT2 on 7q35-36, and LQT3 on 3p21-24. Here we report genetic linkage between LQT3 and polymorphisms within SCN5A, the cardiac sodium channel gene. Single strand conformation polymorphism and DNA sequence analyses reveal identical intragenic deletions of SCN5A in affected members of two unrelated LQT families. The deleted sequences reside in a region that is important for channel inactivation. These data suggest that mutations in SCN5A cause chromosome 3-linked LQT and indicate a likely cellular mechanism for this disorder.
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            The role of disturbed pH dynamics and the Na+/H+ exchanger in metastasis.

            Recent research has highlighted the fundamental role of the tumour's extracellular metabolic microenvironment in malignant invasion. This microenvironment is acidified primarily by the tumour-cell Na(+)/H(+) exchanger NHE1 and the H(+)/lactate cotransporter, which are activated in cancer cells. NHE1 also regulates formation of invadopodia - cell structures that mediate tumour cell migration and invasion. How do these alterations of the metabolic microenvironment and cell invasiveness contribute to tumour formation and progression?
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              The matrix corroded: podosomes and invadopodia in extracellular matrix degradation.

              Podosomes and invadopodia are unique actin-rich adhesions that establish close contact to the substratum but can also degrade components of the extracellular matrix. Accordingly, matrix degradation localized at podosomes or invadopodia is thought to contribute to cellular invasiveness in physiological and pathological situations. Cell types that form podosomes include monocytic, endothelial and smooth muscle cells, whereas invadopodia have been mostly observed in carcinoma cells. This review highlights important new developments in the field, discusses the common and divergent features of podosomes and invadopodia and summarizes current knowledge about matrix-degrading proteinases at these structures.
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                Author and article information

                Contributors
                Journal
                Front Pharmacol
                Front Pharmacol
                Front. Pharmacol.
                Frontiers in Pharmacology
                Frontiers Media S.A.
                1663-9812
                29 July 2015
                2015
                : 6
                : 152
                Affiliations
                [1] 1Inserm UMR1069, Nutrition, Croissance et Cancer, Université François-Rabelais de Tours Tours, France
                [2] 2Département de Physiologie Animale, UFR Sciences and Techniques, Université François-Rabelais de Tours Tours, France
                [3] 3Department of Clinical Research, University of Bern Bern, Switzerland
                [4] 4Inserm U1046, Université de Montpellier Montpellier, France
                Author notes

                Edited by: Jean-François Desaphy, University of Bari Aldo Moro, Italy

                Reviewed by: William Brackenbury, University of York, UK; Sigrid A. Langhans, Alfred I. duPont Hospital for Children, USA

                *Correspondence: Sébastien Roger, Inserm UMR1069, Nutrition, Croissance et Cancer, Université François-Rabelais de Tours, 10 Boulevard Tonnellé, 37032 Tours, France sebastien.roger@ 123456univ-tours.fr ;
                Jean-Yves Le Guennec, Inserm U1046, Centre National de la Recherche Scientifique UMR 9214 PhyMedExp, Université de Montpellier, Centre Hospitalier Universitaire Arnaud de Villeneuve, Bâtiment Crastes de Paulet, 371 Avenue du Doyen Gaston Giraud, 34295 Montpellier Cedex 5, France jean-yves.le-guennec@ 123456inserm.fr

                This article was submitted to Pharmacology of Ion Channels and Channelopathies, a section of the journal Frontiers in Pharmacology

                †These authors have contributed equally to this work.

                Article
                10.3389/fphar.2015.00152
                4518325
                26283962
                a4a6cf69-e1a0-40ab-82a9-66b9bd976898
                Copyright © 2015 Roger, Gillet, Le Guennec and Besson.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 09 June 2015
                : 09 July 2015
                Page count
                Figures: 2, Tables: 1, Equations: 0, References: 185, Pages: 22, Words: 18011
                Funding
                Funded by: Ministère de la Recherche et des Technologies
                Funded by: Ligue Nationale Contre le Cancer
                Funded by: Association CANCEN
                Categories
                Pharmacology
                Review

                Pharmacology & Pharmaceutical medicine
                voltage-gated sodium channel,cell excitability,cancer,sodium,invasion

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