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      Membrane potential and cancer progression

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          Abstract

          Membrane potential ( V m ), the voltage across the plasma membrane, arises because of the presence of different ion channels/transporters with specific ion selectivity and permeability. V m is a key biophysical signal in non-excitable cells, modulating important cellular activities, such as proliferation and differentiation. Therefore, the multiplicities of various ion channels/transporters expressed on different cells are finely tuned in order to regulate the V m . It is well-established that cancer cells possess distinct bioelectrical properties. Notably, electrophysiological analyses in many cancer cell types have revealed a depolarized V m that favors cell proliferation. Ion channels/transporters control cell volume and migration, and emerging data also suggest that the level of V m has functional roles in cancer cell migration. In addition, hyperpolarization is necessary for stem cell differentiation. For example, both osteogenesis and adipogenesis are hindered in human mesenchymal stem cells (hMSCs) under depolarizing conditions. Therefore, in the context of cancer, membrane depolarization might be important for the emergence and maintenance of cancer stem cells (CSCs), giving rise to sustained tumor growth. This review aims to provide a broad understanding of the V m as a bioelectrical signal in cancer cells by examining several key types of ion channels that contribute to its regulation. The mechanisms by which V m regulates cancer cell proliferation, migration, and differentiation will be discussed. In the long term, V m might be a valuable clinical marker for tumor detection with prognostic value, and could even be artificially modified in order to inhibit tumor growth and metastasis.

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          Most cited references131

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          Calcium flickers steer cell migration.

          Directional movement is a property common to all cell types during development and is critical to tissue remodelling and regeneration after damage. In migrating cells, calcium has a multifunctional role in directional sensing, cytoskeleton redistribution, traction force generation, and relocation of focal adhesions. Here we visualize high-calcium microdomains ('calcium flickers') and their patterned activation in migrating human embryonic lung fibroblasts. Calcium flicker activity is dually coupled to membrane tension (by means of TRPM7, a stretch-activated Ca(2+)-permeant channel of the transient receptor potential superfamily) and chemoattractant signal transduction (by means of type 2 inositol-1,4,5-trisphosphate receptors). Interestingly, calcium flickers are most active at the leading lamella of migrating cells, displaying a 4:1 front-to-rear polarization opposite to the global calcium gradient. When exposed to a platelet-derived growth factor gradient perpendicular to cell movement, asymmetric calcium flicker activity develops across the lamella and promotes the turning of migrating fibroblasts. These findings show how the exquisite spatiotemporal organization of calcium microdomains can orchestrate complex cellular processes such as cell migration.
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            Role of ion channels and transporters in cell migration.

            Cell motility is central to tissue homeostasis in health and disease, and there is hardly any cell in the body that is not motile at a given point in its life cycle. Important physiological processes intimately related to the ability of the respective cells to migrate include embryogenesis, immune defense, angiogenesis, and wound healing. On the other side, migration is associated with life-threatening pathologies such as tumor metastases and atherosclerosis. Research from the last ≈ 15 years revealed that ion channels and transporters are indispensable components of the cellular migration apparatus. After presenting general principles by which transport proteins affect cell migration, we will discuss systematically the role of channels and transporters involved in cell migration.
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              Ion channels and the hallmarks of cancer.

              Plasma membrane (PM) ion channels contribute to virtually all basic cellular processes and are also involved in the malignant phenotype of cancer cells. Here, we review the role of ion channels in cancer in the context of their involvement in the defined hallmarks of cancer: 1) self-sufficiency in growth signals, 2) insensitivity to antigrowth signals, 3) evasion of programmed cell death (apoptosis), 4) limitless replicative potential, 5) sustained angiogenesis and 6) tissue invasion and metastasis. Recent studies have indicated that the contribution of specific ion channels to these hallmarks varies for different types of cancer. Therefore, to determine the importance of ion channels as targets for cancer diagnosis and treatment their expression, function and regulation must be assessed for each cancer. Copyright 2010 Elsevier Ltd. All rights reserved.
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                Author and article information

                Journal
                Front Physiol
                Front Physiol
                Front. Physiol.
                Frontiers in Physiology
                Frontiers Media S.A.
                1664-042X
                21 June 2013
                17 July 2013
                2013
                : 4
                : 185
                Affiliations
                Department of Biology, University of York York, UK
                Author notes

                Edited by: Annarosa Arcangeli, University of Florence, Italy

                Reviewed by: Carmen Valenzuela, Instituto de Investigaciones Biomédicas CSIC-UAM, Spain; Teresa Giraldez, University Hospital NS Candelaria, Spain

                *Correspondence: William J. Brackenbury, Department of Biology, University of York, Wentworth Way, Heslington, York, O10 5DD, UK e-mail: william.brackenbury@ 123456york.ac.uk

                This article was submitted to Frontiers in Membrane Physiology and Membrane Biophysics, a specialty of Frontiers in Physiology.

                Article
                10.3389/fphys.2013.00185
                3713347
                23882223
                1edb0918-7cf1-4878-8a64-b69a4c19bf5e
                Copyright © 2013 Yang and Brackenbury.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.

                History
                : 15 May 2013
                : 28 June 2013
                Page count
                Figures: 5, Tables: 0, Equations: 1, References: 147, Pages: 10, Words: 8707
                Categories
                Physiology
                Review Article

                Anatomy & Physiology
                cancer,cell cycle,differentiation,ion channel,membrane potential,migration,proliferation,stem cell

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