Abstract
The purpose of this manuscript is to propose a mechanism for a cancer cure claim resulting from exogenous stimulation of cancer tumors by very intense pressure pulses (VIPPs) treatments from commercially available energy hardware (CellSonic). Could it be that exogenous continuous pulsating waves alter the cellular lipid bilayer; and this in turn also influence intracellular cell signaling? In Vitro experiments are presented supporting the above-stated thesis. The evidence will show via in vitro experiments how trapping energy from bursting oxygen bubbles induces static electricity discharges up to causing luminescence of intracellular lipid droplets. Figures and video recordings documenting the above-mentioned phenomena are presented. In summary, proposed is a mechanism explaining a cancer cure claim via VIPPs.
 1 AAE: Idealized, designed wrote manuscript and conducted in vitro experiments possibly demonstrating a mechanism for VIPPs cancer cure.
 2 SH: Added theoretical principles in the discussion supporting the proposed VIPPs mechanism to cancer cure.
Highlights
The lipid protein interaction has been observed in biological membranes as quoted “Lipid molecules bound to membrane proteins are resolved in some high-resolution structures of membrane proteins
The very first question in this manuscript stated: Could it be that exogenous continuous pulsating waves alter lipid molecules metabolism and structure present in lipid bilayer cell membranes? The in vitro experiments shown above are in support of an electrical phenomenon altering lipid molecules metabolism, in theory causing cancer cells apoptosis
The inability of cancer cells to handle the biophysical properties of changes in cell surface charges, resting membrane potential, alterations of voltage-dependent gating of ion channels, membrane disruption and increased inward electric current density is part of the answer
Summary
The lipid protein interaction has been observed in biological membranes as quoted “Lipid molecules bound to membrane proteins are resolved in some high-resolution structures of membrane proteins. An analysis of these structures provides a framework within which to analyze the nature of lipid-protein interactions within membranes. Membrane proteins are surrounded by a shell or annulus of lipid molecules, equivalent to the solvent layer surrounding a water-soluble protein. The lipid bilayer extends right up to the membrane protein, with a uniform thickness around the protein [1]. A change in lipid metabolism and structure should have an effect on the adjacent membrane proteins metabolism (transduction), interrupting cell signaling up to and including apoptosis. As a corollary the absence of protein transduction is the norm
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