Voltage-gated potassium channels Kvl.3-potentially new molecular target in cancer diagnostics and therapy

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Abstract

Voltage-gated potassium channels, Kvl.3, which were discovered in 1984, are integral membrane proteins which are activated ("open") upon change of the cell membrane potential, enabling a passive flux of potassium ions across the cell membrane. The channels are expressed in many different tissues, both normal and cancer. Since 2005 it has been known that the channels are expressed not only in the plasma membrane, but also in the inner mitochondrial membrane. The activity of Kvl.3 channels plays an important role, among others, in setting the cell resting membrane potential, cell proliferation, apoptosis and volume regulation. For some years, these channels have been considered a potentially new molecular target in both the diagnostics and therapy of some cancer diseases. This review article focuses on: 1) changes of expression of the channels in cancer disorders with special regard to correlations between the channels' expression and stage of the disease, 2) influence of inhibitors of Kvl.3 channels on proliferation and apoptosis of cancer cells, 3) possible future applications of Kvl.3 channels' inhibitors in therapy of some cancer diseases. In the last section, the results of studies performed in our Laboratory of Bioelectricity on the influence of selected biologically active plant-derived compounds from the groups of flavonoids and stilbenes and their natural and synthetic derivatives on the activity of Kvl.3 channels in normal and cancer cells are reviewed. A possible application of some compounds from these groups to support therapy of cancer diseases, such as breast, colon and lymph node cancer, and melanoma or chronic lymphocytic leukemia (B-CLL), is announced

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Teisseyre, A., Gąsiorowska, J., & Michalak, K. (2015). Voltage-gated potassium channels Kvl.3-potentially new molecular target in cancer diagnostics and therapy. Advances in Clinical and Experimental Medicine, 24(3), 517–524. https://doi.org/10.17219/acem/22339

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