Part 6 DNA Pirates of the Sacred Spiral ... DNA and the Electrodynamics of Cancer

So I read this chapter, and it really shows me why I can no longer find any sympathy for the 1 percent. Who appointed these people to monitor the population, who the hell do they think they are that they can decide what the correct if any of the population of this planet should be! I am totally tired of these 'greeners' yakking about the planet, without pointing out who is polluting the planet. Takes a great deal of money to talk about the amount of pollution we are talking about here. They have been on this population trip, my whole life. There should be no amnesty for these people for what they have done to the planet and it's people. Without doubt the people should decide their fate as the people are the ones affected the most with these killer jabs of the last two years. 

DNA: 

Pirates of the Sacred Spiral 

By Dr. Len Horowitz

Chapter 7. 

DNA and the Electrodynamics of Cancer 

“More effective techniques for the control of population growth are at hand. The genetic code has been deciphered, and the elements of DNA can now be made synthetically. . . . Science . . . whatever its problems, including the apprehension of a popular revulsion against its untoward consequences . . . is an enterprise too dynamic to be ‘turned off.’” 

Everett Case, President 

Alfred P. Sloan Foundation 

Annual Report, Spring 1968

In the previous two chapters, the electrodynamics of human biology was discussed. We advanced mechanisms for DNA’s electromagnetic expression. We also introduced cancer and its biochemical and bioelectric antecedents. This chapter takes these subjects to the next level with a strict focus on cancer. 

The genetic-electrodynamics of cancer involves several areas of research including mineral and water abnormalities, tumor cell differentiation, oxygen and pH levels impacting gene expression and genetic repair, metabolic pathways for energy production, protein chemistry, molecular biology and more. 

We will begin by examining mineral and water abnormalities that impact DNA expression and cancer along with the roles played by sodium, potassium, magnesium, and calcium affecting cell membrane potentials during malignant transformation. This will review foundational discussions upon which more technical knowledge can be advanced regarding the important roles played by cell membrane components in health versus malignancy. 

As introduced in previous chapters, the cell membrane is a dividing structure that maintains biochemically distinct compartments between the inside (intracellular) and outside (extracellular) spaces.(Marieb 1998) 

The lipid structure of cell membranes makes them relatively impermeable to the passage of charged molecules. As a result, charged molecules must cross through ion channels within the membranes to enter or leave cells. 

Ion channels are transmembrane protein molecules that contain aqueous pores connecting the inside of the cell to the extracellular space. These channels can open and shut in response to a variety of signals. The passage of charged molecules through ion channels in the cell membrane endows the membrane with a critical electrical conductive property allowing for inward and outward current flows.(Aidley and Stanfield, 1996). This is one factor that establishes electrical circuits within biological tissues. 

More Membrane Electrodynamics 

Based on forthcoming information in this chapter, it is reasonable to suggest a spiral or coiled design of these transmembrane protein molecules. This is consistent with the design of other protein members of the liquid crystal cytoskeleton. Moreover, such a design would energize the movement of charged elements such as transiting ions. 

In order to maintain electrolyte balance in intracellular fluid (ICF), water, sodium, and potassium are in constant motion between the intracellular and extracellular compartments.(Edwards 1998) Extracellular fluid (ECF) and ICF contains different concentrations of minerals. Minerals carrying positive charges are called cations. In order to maintain electric neutrality, negatively charged molecules called anions must match these cations in concentration. Sodium is the main cation of ECF, whereas potassium is the major cation of ICF. Chloride and bicarbonate are the main anions of ECF, while proteins and organic phosphates are the main anions of ICF. Uncharged molecules such as glucose or urea are also present in both compartments and contribute to the osmotic gradients or flow of liquids and solids between the ECF and ICF.(Edwards, 1998) 

As discussed at the end of Chapter 5, the passage of electrically charged ions through a membrane will create a flow of electric currents through the membrane. These ions, in turn, will affect the metabolism of the cell and the potential of the cell membrane. 

All body cells, thus, carry a weak electric current flowing through them. These resonate with bioelectrical circuits energizing the entire organism.(Stanish, 1985) 

Overall mineral, water, and membrane changes in cancerous tissues play important roles in changing the cellular geometry, metabolic biochemistry, and electrical properties of cancer cells. 

Dr. Keith Brewer reported that intracellular calcium and magnesium concentrations were lowered in cancer cells due to impaired membrane transport.(Brewer, 1985) According to Brewer, the transport of substances across the cell membrane is controlled by: the electrical properties of the chemical bonds on and in the membrane, the electrical gradient across the membrane, and the electrical attractions between positively charged cations and polar molecules with positive and negative regions.(Brewer and Passwater, 1976) 

Earlier we referred to F.W. Cope who described a characteristic pattern of electrolyte and fluid abnormalities that occur in any tissue that is damaged. He calls this pattern the “tissue damage syndrome.” When cells are injured from any cause, cells will lose potassium, and accumulate sodium and water.(Cope, 1978) 

Advanced research by Cope showed that proteins of a healthy cell exist in a normal electronic configuration state where a significant portion of cell water is structured or bound in concentric  rings around these protein molecules. In addition, when the proteins are in their healthy configuration, the negatively charged sites on the protein matrix have a greater preference for association with potassium rather than with sodium .(Cope, 1978) If these findings are accurate, this may be one of the factors that accounts for the finding that healthy cells have high cell potassium and low intracellular sodium concentrations. 

Having also referred to transmembrane proteins, these consist of linear chains of amino acid residues with attached carbohydrate and/or lipid molecules. The electro attractive and repulsive forces between these components, and the external or internal saltwater environment, cause these proteins to fold into three-dimensional shapes called conformational states. Protein function is dependent on these conformational states. The cell membrane and its associated membrane proteins are dynamically active with the associated proteins undergoing continuous changes in shape and bioelectric activity. In proteins that are enzymes the conformational state determines whether or not the enzyme will expose its ligand binding sites to catalyze metabolic reactions. 

If the membrane protein is an ion channel the conformational structure will determine whether the channel is open or closed. When the channel is open, it is able to pass ions such as potassium, sodium, chloride, and calcium, across the cell membrane.(Hille, 1992) 

Moreover, the ability of the cell proteins to stay in their normal configurational state depends on the cell being free from chemical, physical, or hypoxic damage. When physical, chemical, or hypoxic damage occurs to a cell, many cell proteins will change to an abnormal or damaged configurational state. In that pathological state “the cell proteins lose their preference for association with potassium rather than sodium, and lose much of their ability to structure water.”(Cope, 1978) 

Water also transforms its electro-capacitance along with its structured form by flowing through spiraling vortices. It maintains its structured form as a result of electromagnetic capacitance related to its therapeutic capacitance. (Lorenzen and Horowitz, 1999) In addition, as the water content and the percentage of unbound water within cells increase, the cells swell. (Ling and Ochsenfeld, 1976) These changes alter their transmembrane ionic and electrical gradients. When these protein intoxication changes occur, potassium leaves the cell and is replaced by sodium. (See additional details in figure 7.1.) 

Membrane Water Structuring 

Proteins can also be induced to resume their normal configuration by measures that increase the intracellular concentration of potassium, magnesium, and ATP. This alone, interesting enough, will result in cell water becoming more structured, and will cause the cell to release unstructured cell water and sodium.(Cope, 1978) Besides this, magnesium is also involved in maintaining the intracellular concentration of potassium. 

Dr. Horowitz has theorized that the structuring of water in this way may depend on the ATP more than the elements potassium or magnesium. The ATP carries an electron charge with related frequencies that may help direct the form of water structuring. 

The structuring of water around intracellular proteins will also affect the configurational state, liquid crystal state, and electrical properties of these proteins. (Figure 7.2. explains more about liquid crystals including their influence on DNA expression.) Structured or bound water has less freedom of movement than unbound water. 

Nuclear magnetic resonance (NMR) can be used to measure the amount of water that is structured in normal versus cancerous cells. Hazelwood and his colleagues showed in a 1974 NMR study that malignant tissues have significantly increased amounts of unbound water compared to normal tissues.(Hazelwood, 1984) 

Fig. 7.1. DNA/Membrane Electro Communications 

So far we have established that cell membranes have an electronic character and cancer cells have dysfunctional cell membranes. Healthy cells of the body do not operate in isolation. They are continuously communicating with other cells. Cancer cells, however, lose their ability to communicate with other cells and regulate their growth independently in response to this failed communication including energetic dissonance. 

Dr. Merrill Garnett has advanced the understanding that an alternating current oscillating circuit exists inside of cells between the cell membrane and the DNA. This energy is conducted over electronic liquid crystal (LC) protein polymers inside the cell. This circuit is activated during differentiation to trigger the expression of genes.(Garnett et al., 2002) Garnett’s findings appear to show that cells use their electrical properties to moderate gene expression! As part of his evidence, Dr. Garnett has reported that normal cell development requires normal energy flows. 

Electrical charges stored in the cell membrane (capacitance), and electrical charges of oxygen free radicals, are normally transferred to DNA and are involved in DNA activation and the creation of an electrical field around DNA. DNA is very effective in transferring large amounts of electrical charge along its long axis.(Garnett, 1998) In fact new research shows that DNA molecules may be good molecular semiconductors.(Li and Yan, 2001) 

An electrical pathway from the cell membrane to DNA is a natural pathway related to development in cells that use aerobic mechanisms with ATP production.(Garnett, 1998) As a corollary, this natural electrical pathway is transiently disrupted in healthy cells while they are involved in wound healing, and permanently disrupted in cancer cells that rely on anaerobic glycolysis for energy production. 

These changes in the degree to which water is structured in a cell or in the ECM will affect the configurations and liquid crystal properties of proteins, cell membranes, organelle membranes, and DNA. Healthy tissues simply have more structured water than unhealthy tissues. Clinicians who recognize this fact have found that certain types of music, toning, chanting, tuning forks, singing bowls, magnetic waters, certain types of frequency generators, phototherapy and spectrochrometry treatments, and homeopathics, correctly used, can enhance water structuring in your tissues and subsequently improve health. 

Cancerous Conditions 

At any given moment, everyone maintains numerous cancer cells. A number of features such as changes in the mineral concentrations inside of these cell, the degree that water is structured therein, and an excess of negative electrical charges on their exterior surfaces, cause the cell membrane potential of these cancerous cells to be less than normal.(Cone, 1970) 

As previously mentioned, cancerous tissues, and less differentiated regenerating tissues, are more electronegative than normal cells and tissues.(Ambrose et al., 1969; Schaubel et al., 1970; Becker, 1985) As a result of increased intracellular sodium, cancer cells will retain more water causing them to be more spherical and have different geometry than normal cells. When cells become swollen with too much water, normal cell signaling mechanisms are disrupted, aerobic cellular metabolism of sugars is inhibited, and ATP energy production falls. 

Researchers now believe that genetic mitosis is partly regulated by intracellular sodium levels. Investigators have postulated that an adverse intracellular sodium/potassium ratio affects the transmembrane potential of malignant cells and predisposes to malignant mitogenesis.(Cone, 1975; Regelson, 1980; Haltiwanger, 2002) 

Fig. 7.2. Diagrams of Liquid Crystal Phases 

Cholesteric Phases Smectic Phases Nematic Phases 

Liquid crystal research began in 1888 with Friedrich Reinitzer, an Austrian botanist. Subsequent research determined that liquid crystal materials have common characteristics including: a rodlike molecular structure, rigidness of the long axis, strong dipoles and/or easily polarizable substituents, and spiraled designs. 

Liquid crystalline molecules (mesogens) point along a common axis, called the director. This is in contrast to molecules in the liquid phase which have no intrinsic order. In the solid state, molecules are highly ordered and have little translational freedom. 

“It is sometimes difficult to determine whether a material is in a crystal or liquid crystal state. Crystalline materials demonstrate long range periodic order in three dimensions. By definition, an isotropic liquid has no orientational order. Substances that aren’t as ordered as a solid, yet have some degree of alignment are properly called liquid crystals.” Thus, liquid crystalline structures are described using: 1) positional order; 2) orientational order and 3) bond orientational order. “Positional order refers to the extent to which an average molecule, or group of molecules, shows translational symmetry (as crystalline material shows). Orientational order... represents a measure of the tendency of the molecules to align along the director on a long-range basis. Bond orientational order describes a line joining the centers of nearest-neighbor molecules without requiring a regular spacing along that line. 

Most liquid crystal compounds exhibit polymorphism,...where more than one phase is observed. Distinct phases of matter are observed between the crystalline (solid) state, “mesophases,” and isotropic (liquid) states. Liquid crystal types depend on the amount of order in the material including: 1) Nematic Phases wherein the liquid crystal is characterized by molecules that have no positional order but tend to point in the same direction (along the director). Liquid crystals are anisotropic materials with varying physical properties depending on the average alignment with the director. If the alignment is large, the material is very anisotropic. Similarly, if the alignment is small, the material is almost isotropic. A special class of nematic liquid crystals is called chiral nematic. Chiral refers to the unique ability to selectively reflect one component of circularly polarized light. The term chiral nematic is used interchangeably with cholesteric. 2) Smectic (i.e., “slippery”) phases show molecular translational order not present in the nematic. In the smectic state, molecules maintain general orientational order, but also tend to align themselves in layers or planes. Motion is restricted within these planes, and separate planes are observed to flow past each other. The increased order means that the smectic state is more “solid-like” than the nematic. 

As many as 12 smectic phase variations have been identified. Some of these share organizational characteristics with DNA. In the smectic-B mesophase, for instance, molecules are arranged into a network of hexagons within layers. In the smectic-C mesophase, molecules are tilted from layer to layer forming a helix. This coiling apparently plays a role in electro-conductivity, light and energy field transmissions. Cholesteric phases, also called chiral nematic liquid crystals, also produce intermolecular forces. In these DNA-like structures, the directors actually form in a continuous helical pattern. The “pitch” of these structures are defined as the distance it takes for the director to rotate one full turn in the helix. 

 “A by-product of the helical structure of the chiral nematic phase, is its ability to selectively reflect light of wavelengths equal to the pitch length, so that a color will be reflected when the pitch is equal to the corresponding wavelength of light in the visible spectrum. The effect is based on the temperature dependence of the gradual change in director orientation between successive layers of pitch, by increasing the temperature of the molecules, hence giving them more thermal energy.... [Industrially,] various types of these liquid crystals are often used to create sensors with a wide variety of responses to temperature change. Such sensors are used for thermometers often in the form of heat sensitive films to detect flaws in circuit board connections, fluid flow patterns, condition of batteries, the presence of radiation, or in novelties such as “mood” rings. 

Another type of liquid crystal (i.e., Columnar Phases) is characterized by stacked columns of molecules. The columns are packed together to form a two-dimensional crystalline array.”

DNA itself demonstrates several liquid crystal types and functions.

See: Davidson and Rill, “Multiple liquid crystal phases of DNA at high concentrations” at 

http://micro.magnet.fsu.edu/publications/pages/nature.html and also, http://www. iq.usp.br/wwwdocentes/mralcant/AboutLC.html. 

Interdependent Risk Factors in Gene

Controlled Malignant Transformation 

Risk factors for gene-controlled malignancies include hypoxia and low cellular pH. These factors can affect: gene expression, genetic stability, genetic repair, protein structures, protein activity, intracellular mineral concentrations, and types of metabolic pathways used for energy production. 

Cancerous tumors are composed of cell populations that range from highly aggressive undifferentiated cells to well differentiated cells. In general, tumors with highly undifferentiated cells are more invasive than tumors composed of well-differentiated cells or tumors with mixed cell populations. Some cancers are almost completely composed of undifferentiated cells that are biochemically similar to embryonic cells. This is largely due to increased expression of embryonic genes. Highly undifferentiated tumors typically produce gene products such as proteins like alpha-fetoprotein (AFP) and carcinoembryonic antigen (CEA), and enzymes and hormones such as human chorionic gonadotropin (hCG) that are characteristic of embryonic tissues. On the other hand, tumors with well-differentiated cells will produce gene products more closely resembling normal adult tissues. 

Increased malignant behavior during tumor growth is also affected by the microenvironment of tumors, which besides being characterized by areas of both acute and chronic hypoxia and low pH, is deprived of nutrients and is electrochemically altered.(Moulder et al., 1987; Rockwell, 1992) 

Oxygen Reduction and Carcinogenesis 

The severity of hypoxia and acidosis in tumors can affect tumor cell invasiveness, metastasis, risk of recurrence, and resistance to chemo and radiation therapies.(Teicher, 1994; Rofstad, 2000) 

Tumors exist in a dynamic state of competition for survival wherein oxygen delivers life energy. To conquer healthy terrain, tumors continually secrete growth factors that initiate the formation of new blood vessels to feed on oxygen for their continued expansion. Yet, some tumors grow so rapidly that they out grow their blood supply, large tumors often have areas that are poorly oxygenated (hypoxic) and other areas that are well oxygenated.(Vaupel et al., 1991) Hypoxic and well-oxygenated areas may fluctuate coming and going as blood vessels form and then regress.(Holash et al., 1999) 

Tumors with areas of mixed oxygenation will often contain heterogeneous groups of cells that exhibit biochemical diversity. The same tumor will have some cells that are utilizing different metabolic reactions to create energy than other groups of cells in the same tumor. This is one reason why different cell populations in the same tumor will respond differently to treatment measures. Some cells will be killed by some treatments while other cells will survive and in a sense be selected for further growth.(Gray et al., 1953; Graeber et al., 1996) 

Fluctuating oxygen levels will result in fluctuations in the types of genes that are activated, types of proteins (e.g., enzymes) that are produced, and the types of metabolic reactions that occur.(Dang et al., 1997) Fluctuations in the types of metabolic reactions used to create energy will result in variations in lactic acid production, acid excretion, and acid accumulation, both within cells and within the ECM. 

Earlier we explained the concept of electrical cloaking by tumor cells against immune defense cells. If you have ever wondered why tumor cells resist host immune defenses, consider this also. In vitro studies have shown that tumor cell surface adhesion molecules are electrochemically “down regulated” upon exposure to hypoxia conditions.(Hasan et al., 1998). This means that hypoxia can result in decreased cell adhesion of tumor cells to the ECM. Loss of contact with the ECM permits tumor cells to spread to more distant locations, and reduces the ability of the ECM to exert growth inhibition. It also reinforces the concept of cancers developing an electrochemical barrier to immune attack. 

Some researchers have focused on the finding that the hypoxic and acidic microenvironment of tumors will create further genetic instability and mutations.(Reynolds et al., 1996) Hypoxia and acidic tumor microenvironments will cause certain genes to become activated and expressed, while other genes may become inactivated so that the metabolic reactions within tumor cells will be altered. These conditions can also create DNA damage and impair DNA electrochemical repair mechanisms.(Yuan et al., 1998, 2000) For example, low intracellular pH has been shown to alter the conformational structure and function of cellular proteins, including DNA polymerases.(Eckert and Kunkel, 1993) These enzymes play a major role in protein synthesis and cellular repair. 

One common characteristic of many tumors is the reduced activity of a special protein called p53 that is involved in triggering cell death. Hypoxic conditions will favor selection of immortalized tumor cells with reduced apoptotic (i.e., planned cell death) potential.(Graeber et al., 1999) 

As previously introduced, hypoxic tumor cells often lack enough oxygen to activate their aerobic metabolic pathways to supply their energy needs.(Rossi-Fanelli et al., 1991) Tumor cells in hypoxic conditions will, thus, convert most of their pyruvate to lactate instead of to acetyl Coenzyme A.(Warburg, 1956) This type of energy production is very inefficient; so tumors require much larger amounts of sugar in order to maintain their energy production. Tumor cells, in a sense, become sugar junkies. This fact alone can have profound implications for nutritional therapy and cancer reversals.

Cancer Cells and Sugar Energetics 

Tumor cells express several adaptations in order to sustain their sugar addiction and metabolic strategies to address this aberration. Tumor cells develop larger numbers of glucose receptors and transporters on their cell surfaces in order to increase their sugar uptake.(Van Winkle, 1999) 

Given this increased sugar dependence of cancer cells, it is appalling the health-enhancing natural sweetener (i.e., sugar substitute) stevia has become increasingly regulated in recent years while carcinogenic, and otherwise toxic, artificial sweeteners have been increasingly endorsed by chemical pharmaceutical and cancer industry profiteers in association with government regulatory agencies including the FDA. 

Another fact is, hypoxia stimulates the transcription of numerous genes, including genes that code for enzymes of the glycolytic pathway and cell membrane glucose transport proteins—GLUT-1 and GLUT-3. Using this knowledge as a basis for therapy, the administration of cesium salts has been reported to limit tumor cell uptake of glucose, which starves cancer cells and reduces their ability to make energy by fermentation.(Semenza, 2002) 

When it was first discovered that tumors mostly use anaerobic metabolism of glucose—two simple sugar molecules (i.e., sucrose)—it was thought that providing more oxygen would convert tumors back to aerobic metabolism.(Warburg, 1930) Unfortunately, after doing this, tumors still exhibited high levels of glycolysis.(Weinhouse, 1976). 

Here is more beneficial therapeutic advice. Tumor cells also increase their activity of the intracellular enzyme called glucokinase. This enzyme sequesters sugar inside of the cell.(Board et al., 1995) An extract of avocado called mannoheptulose may be helpful. It has been found to inhibit glucose entry into tumor cells and reduce the activity of this glucokinase. So if you want to help starve cancers, eat organic avocados! 

Fig. 7.3. Cell Membrane Treatments in Cancer 

Normalizing the electrical potential of cell membranes through directed mineral therapy can be used to increase the abnormally low transmembrane potential of cancer cells and injured tissues. Effects that are seen when membrane potential is increased include: enhanced cellular energy (ATP) production, increased oxygen uptake, changes in entry of calcium, movement of sodium out of the cells, movement of potassium into the cells, changes in enzyme and biochemical activity, and changes in cellular pH. 

2-AEP (2-aminoethylphosphoric acid) mineral transporters enhance cell membrane capacitance in several ways. First by repairing damaged cell membranes and second by effectively delivering minerals to the outer surface of cell membranes. 

The orotate, aspartate, and arginate mineral transporters are advanced mineral delivery systems that effectively deliver minerals into the interior of cells. Mineral delivery into the cell interior is important because many of the cell’s cytoplasmic and mitochondrial enzymes require minerals in order to be activated. 

Cancer cell membranes also have altered lipid/sterol content.(Revici, 1961) In addition, the types of glycoproteins and antigens that they express are different.(Warren et al., 1972; Hakomori, 1990)

The lipid/sterol composition of cell membranes also affects membrane fluidity. Fluidity is abnormal in cancer cells and is increased to its highest level during cell division. Normalization of membrane fluidity (membrane repair) can decrease the growth of tumors. Magnesium arginate, the amino acid taurine, vitamin C, vitamin A, and beta carotene all have been shown to help normalize membrane fluidity and membrane potential in cancer cells. Cell membrane repair can also be initiated by using lipid and sterol compounds such as 2-AEP, essential fatty acids, sterols, and phytosterols. NL Sterols Lipids  

Some tumor cells express glycoproteins that promote protein breakdown and, from this, sugar production.(Stipanuk, 2000) How is this possible? Through the secretion of enzymes called cytokines, especially tumor necrosis factor, which increases in cancer. Some of these cytokines increase the breakdown of normal tissue proteins.(Bender, 2002) The amino acids released by protein breakdown can then be used in gluconeogenesis (i.e., new sugar production). Thus, tumor necrosis factor not only promotes protein breakdown, and with this the destruction of normal tissues, but it also increases gluconeogenesis for cancers’ sugar addiction.(Bender, 2002) 

Many tumor cells will produce lactate when they metabolize glucose anaerobically. The lactate is exported from the tumor cells and then utilized by the liver, here again, for gluconeogenesis.(Bender, 2002) In this way, even more sugar for tumor growth is produced. 

Overall gluconeogenesis is stimulated when cancer is present. Gluconeogenesis requires a great deal of energy. For this reason, excessive gluconeogenesis is thought to be a significant factor that contributes to the wasting syndrome that accompanies cancer called cachexia.(Gold, 1968) 

In the 1960s, this condition was effectively treated by Dr. Joseph Gold, a well known New York oncologist whose work with hydrazine sulfate received international respect. Even then, cancer industry cohorts at the National Cancer Institute (NCI) officially condemned Dr. Gold’s contributions. A U.S. General Accounting Office inquiry, prompted by a congressional investigation, cited the NCI for this gross injustice favoring only cancer profiteers. Thereafter, scientifically vindicated yet politically compromised, Dr. Gold continued to advance metabolic strategies that inhibited the enzyme phosphoenolpyruvate carboxykinase (PEP-CK) based on his finding that this would reduce gluconeogenesis in malignancies, and decrease the severity of cachexia.(Gold, 1968; 1974, 1981)

Tumor Acidification and Related Therapies 

One of the characteristic features of cancers is that cancerous cells rapidly divide and proliferate. In general, growing cancers versus normal tissues have many more cells undergoing mitosis. According to Keith Brewer, normal and malignant cells undergo mitosis between a pH range of 6.5 7.5, and the mitosis rate slows as the intracellular pH approaches the extremes of this range. If a cell can be forced into a pH outside of this range, cell division ceases.(Brewer, 1985) Recognizing this fact serves as an additional basis for cancer control strategies that involve increasing or decreasing the pH of tumor cells. 

Increasing body alkalinity to the higher side of normal (i.e., 7.3 to 7.5 pH) has been highly recommended by advanced oncologists and health practitioners.

Because glycolytic metabolism predominates in tumors, some lactic acid accumulation and intracellular acidification may occur in tumors under hypoxic conditions although most of the lactic acid and hydrogen ions are exported into the ECM leading to acidification of the ECM.(Ojugo et al., 1999) Thus, the extracellular pH around tumor tissues is usually more acidic than the extracellular pH of normal tissues. Extracellular pH levels as low as 7.09 have been measured in some human tumors.(Van der Zee et al., 1989) It is thought that both lactate and hydrogen protons are exported from tumor cells into the extracellular space as a way of limiting intracellular acidity.(Ojugo et al., 1999) 

This theory makes complete sense, as it is reinforced by the finding that tumor cells efficiently sequester and export acids. By so doing, they are often able to maintain their cytoplasmic pH nearly equal to that of normal cells. That is, between 7.0- 7.3 pH.(Newell et al., 1993; Stubbs et al., 1994) 

Intracellular cytoplasmic pH is maintained in tumor cells by sequestering excess acids in cytoplasmic vesicles, and through cell membrane mechanisms that include a sodium hydrogen ion exchanger. 

Fig. 7.4. Mineral Pumps and pH in Cancer 

Mineral pumps in cell membranes help control mineral concentrations and pH inside and outside of cells. Movement of Na+ and K+ cations through cell membranes create electric currents in, and just above, the membranes in the glycocalyx-water-membrane interface. The Na/K membrane pump uses ATP created by mitochondrial oxidation of food. 1/3 of ATP energy produced by your body is needed to run these pumps and generators simply to maintain the location of these two minerals in balance with magnesium and potassium. 

But these pumps can fail with hypoxia, injury, and cancer. In these conditions potassium and magnesium will leak out of cells and sodium and water will leak into cells. Cells’ energetic mechanisms and mineral pumps subsequently fail leading to general metabolic disturbances.(Cone, 1975; Cope, 1978; Seeger and Wolz, 1990; Cure, 1991, 1995; Webb et al., 1999; ) 

Mineral transporters that effectively deliver minerals into cells help address these issues. In order to transport potassium and magnesium ions into sick cells to support mitochondrial production of ATP, reactivate mineral pumps, and correct cellular acidosis, these cations should be bound to carrier molecules that can penetrate the cell membrane without disrupting the membrane charge. K+ and Mg+ mineral transporters such as Pot-mag aspartate, magnesium arginate, and potassium arginate, place K+ and Mg+ ions on the inner surfaces of cell membranes. This assists in optimizing the action of Magnesium-dependent ATPase enzymes that are located on the inner surface of the cell membrane.These enzymes, thus, maintain the normal concentration of potassium in the cell removing 3 sodium ions for every 2 potassium ions that are brought in. 

These adjustments also help normalize Krebs’s cycle magnesium and potassium dependent enzymes, ATP, and glucose entry into cells and acid flow out of your cells. Courtesy of Dr. Haltiwanger and http://www.du.edu/~kinnamon/3640/memb_pot_1.html. 

Dr. Haltiwanger has theorized that the buildup of intracellular acids in cytoplasmic vesicles may interfere with mitochondrial production of ATP. The proposed mechanism for this lies in disrupting the hydrogen ion gradient across the mitochondrial membrane. This would create a positive feedback loop where anaerobic glycolysis creates an intracellular acidic condition that further interferes with oxygen-mediated electron transport in the mitochondria. Therefore, in order to maintain energy, anaerobic glycolysis would be selected electrochemically by tumor cells. 

Theory-based cancer control has been performed by tumor hyper acidification. Manfred von Ardenne of Germany was one of the pioneers who, back in the 1960s, began to develop a cancer treatment using intravenous glucose to create increased levels of tumor acidity. He used hyperthermia to kill cancer cells that were already compromised by excessive acidity.(von Ardenne, 1994) Mixed results have been reported since chemotherapies have been used to block the movement of lactate and hydrogen protons from tumor cells. This increased cellular acidification, but failed overall to cure cancers. 

In one study, the bioflavonoid quercitin was found to inhibit the synthesis of heat shock proteins in tumors and to block the export of lactate from tumors creating tumor-toxic levels of intracellular acidity.(Kim et al, 1984) Consequently, the use of quercetin as a cancer treatment became the subject of several patents. Unfortunately, this treatment was proven effective only in the hypoxic portion of tumors. It is generally ineffective in tumors, and areas of tumors, that are not hypoxic. Use of quercetin, it was learned, was most effective when hyperthermic treatments were used concurrently. 

Related approaches to cancer treatment have involved the creation of hyperglycemia (i.e., high blood sugar) and/or hyperthermia. The former was shown to deliver intracellular acidification. A number of researchers have reported on the use of  oral and intravenous glucose as a way to increase tumor acidity with limited efficacy.(Volk et al., 1993; Leeper et al., 1998) Researchers have also shown that extracellular acidification of tumors will enhance the effect of hyperthermia (Gerweck, 1977; Wike-Hooley, 1984; van de Merwe et al, 1993) and inhibit the development of thermotolerance in cultured tumor cells.(Goldin and Leeper, 1981) 

Recently, cancer researchers have continued to study the use of both intracellular and extracellular acidification of tumors to enhance the cytotoxic effects of chemotherapeutic agents.(Atema et al., 1993; Skarsgard et al., 1995; Kuin et al., 1999) 

Tumor Alkalization and Cesium 

Tumor alkalization has also been an area of cancer research and chemotherapeutics. Cesium, for instance, is a naturally occurring alkaline element that was promoted for use in cancer by a scientist named Keith Brewer. Cesium is preferentially taken up by tumor cells.(Brewer, 1985) Use of cesium is thought to reduce the cellular uptake of glucose by cancer cells leading to starvation of the malignancy. Cesium also was reported by Brewer to raise the cell pH of cancer cells up to a lethal range of 8.0. 

Use of cesium in this way has, however, met with mixed results.(Sartori, 1984) Dr. Haltiwanger cautioned those tempted to use this treatment to read extensively about cesium before proceeding due to its limitations and potential side effects.(Haltiwanger, 2002) 

Potassium and Cancer Therapeutics 

Recall that the accumulation of positively charged hydrogen cations inside of cancer cells through either respiratory or metabolic acidosis will shift potassium out of the cells leading to higher than normal levels of potassium in the bloodstream (hyperkalemia), lower than normal potassium intracellularly, and increased potassium loss through the kidneys. 

One researcher, Dr. Gilbert Ling, developed a unique theory regarding the mechanisms used in potassium regulation with therapeutic implications for cancer.(Ling, 2001) He published that the membrane pump theory is wrong. Alternatively, he advanced an association-induction (AI) hypothesis which includes the idea that ATP bonding to intracellular proteins mediates selective and preferential absorption of potassium over sodium.(Ling, 2001) Dr. Ling’s work is highly technical, but very informative. 

Most authorities agree that movement of potassium out from a cell’s interior is regulated by acidity of the cell interior; the permeability of the cell membrane, and chemical and electrical gradients to the potassium ions. 

When cancer cells export hydrogen ions, the ECF space becomes more acidic. The amount of acids produced by cancer cells may even be severe enough to overwhelm the body’s homeostatic pH regulatory mechanisms. 

The cell cytoplasm of malignant cells may or may not be acidic depending on how efficient tumor cells are in sequestering and exporting acids, but the ECM around tumors is typically acidic. By definition, acidic tissues are electron deficient. So a tumor may have areas that have a relative state of electron deficiency. This condition of electron deficiency may help explain why measures that increase electron availability, like magnetized waters, lemon juice, negative ion generators, standing by water falls, standing by the ocean surf, use of electron rich antioxidants, consumption of electron dense foods (fresh vegetables and vegetable juices and essential fatty acids like fresh flax oil), help some people with chronic degenerative conditions and cancers. Clinicians widely know that many chronic degenerative conditions are most often associated with tissue acidity. 

Awareness of such findings gives credence to nutritional approaches to cancer such as the dietary program advocated by the famous Dr. Max B. Gerson. During his lengthy medical career, Dr. Gerson advocated low sodium intake and high potassium supplementation through use of raw vegetable juices and potassium supplementation.(Cope, 1978; Ling, 1983). 

Variables on Cancer Cell Surfaces: 

Implications for Immunity 

Building on earlier discussions, human chorionic gonadotropin (hCG), a natural female pregnancy hormone, sialic acid, as well as negatively charged residues of RNA, give tumor cells a strong negative charge on their cell surface. 

Regarding cancer cell membranes and electrochemistry, as mentioned, all cells have cell surface glycoproteins. As cells specialize, they develop unique sets of cell surface glycoproteins that allow cells of the same type to recognize, communicate, and adhere to each other.(Reichart, 1999) 

These cell surface glycoproteins contain varying concentrations of sialic acid, which is one of the primary molecules responsible for conferring a negative charge to the cell surface of all cells.(Cure, 1995; Acevedo et al., 1998) The chemical characteristics of hCG make it a sialoglycoprotein, that is, much like the sialic acid glycoprotein compound.(Acevedo, 2002) 

It has been repeatedly proposed that the presence of hCG on the surface of cancer cells is a universal marker for cancer.(Acevedo et al., 1995; Acevedo, 2002) According to Dr. Acevedo malignant transformation will cause the genes that code for hCG to become activated causing cancer cells to begin producing this hormone.(Acevedo, 2002) When cancer cells secrete this hormone it collects on the cell surface. Since hCG contains large amounts of sialic acid this results in cancer cells having a stronger cell surface negative charge than normal cells.(Acevedo et al., 1998) 

Dr. Cure presented data that cancer cells are also coated by negatively charged residues of RNA, which is another contributing factor to the strong cell surface negative charge of cancer cells.(Cure, 1991, 1995) He also presented data that suggested bacteria can secrete compounds that increase the negative charge of cells to which they are attached, or bacteria and viruses can cause cells that they infect to secrete compounds that increase the negative charge of the cells. 

Fig. 7.5. Electrodynamics of Cancer “Stealthing”

Cell surface glycoproteins contain varying concentrations of sialic acid, which is one of the primary molecules responsible for conferring a negative charge to the cell surface of all cells.(Cure, 1995; Acevedo et al., 1998). The chemical characteristics of hCG helps turn sialic acid into a sialoglycoprotein which is a cancer risk.(Acevedo, 2002) 

Because immune defense cells, such as natural killer (NK) cells and macrophages, also have a negative surface charge these cells are repulsed by the strong negative electrical field of the sialoglycoprotein on cancer cells when they try to approach and terminate them.(Van Rinsum et al., 1986; Cure, 1995; Acevedo et al., 1998) Negatively charged hCG is also present on the cell membranes of embryonic and fetal cells, sperm cells, and all cancer cells regardless of type or origin. This membrane-associated hCG make all these cells immunologically stealthed.

Human chorionic gonadotropin (hCG), a hormone usually associated with pregnancy, can be found on the surface of all cancer cells and in some reportedly contaminated vaccines. Dr. Acevedo has proposed that the presence of hCG on the surface of cancer cells is a universal marker for cancer.(Acevedo et al., 1995; Acevedo, 2002)

According to Dr. Acevedo, malignant transformation will cause the genes that code for hCG to become activated causing cancer cells to begin producing more of this hormone.(Acevedo, 1998; 2002) When cancer cells secrete this hormone it collects on the cell surface resulting in cancer cells having a stronger cell surface negative charge than normal cells. The surface negatively repels immune cells.

Membrane degeneration also occurs in the initial phase of carcinogenesis first in the external cell membrane and then in the inner mitochondrial membrane. Thus affected, membranes become more permeable to water-soluble substances. Potassium, magnesium, and calcium migrate from the cells and sodium and water accumulate in the cell interior. All of this affects the electrical properties of cells and contributes to electrical “cloaking,” immunological “stealthing,” and ill health.(Seeger and Wolz, 1990)

Because immune defense cells such as natural killer (NK) cells and macrophages (meaning “big eaters’) also have a negative charge, these cells are repulsed by the strong negative electrical field of cancer cells when they try to approach these cells.(Van Rinsum et al., 1986; Cure, 1995; Acevedo et al., 1998). According to Dr. Acevedo, “Since all the normal cells from our immune system—macrophages, NK cells, and B cells, express in their membranes a “normal” negative charge, the high negative charge of hCG and its subunits, demonstrated to be present in the cell membranes of embryonic and fetal cells, in sperm cells in every stage of development, and in all cancer cells irrespective of type or origin as membrane-associated hCG, make all these cells immunologically inert.”(Acevedo, et al., 1998) 

In other words, your body’s premier defense mechanism against infectious diseases and cancers—the immune system—is restricted from approaching, and adhering to, cancer cells since negative charges repel. “That is the reason why the embryo and fetus, which under normal conditions are 50% foreign to the mother, are able to survive immune system attack by the mother, and why sperm cells and cancer cells also survive.” (Acevedo, 2002) 

hCG in Contaminated Vaccines 

Digressing for a moment from this focused science to this subject’s medical sociology, the following 1968 quote from internationally respected professor Paul Ehrlich, author of The Population Bomb, is noteworthy and relevant: 

Our position requires that we take immediate action at home and promote effective action worldwide. We must have population control at home, hopefully through a system of incentives and penalties, but by compulsion if voluntary methods fail. . . . We can no longer afford merely to treat the symptoms of the cancer of population growth; the cancer itself must be cut out.” 

As Dr. Horowitz reported in Death in the Air: Globalism, Terrorism and Toxic Warfare, on Friday, July 11, 1986, United Press International broke world news that the first human tests of an “anti-pregnancy vaccine,” developed by doctors at Ohio State University in Columbus, was about to take place in Australia. The experimental vaccine, the article said, “would act as a contraceptive by immunizing women against a hormone necessary to maintain pregnancy.”(UPI, 1996) 

Dr. Vernon Stevens, Director of Reproductive Biology at Ohio State’s Department of Obstetrics and Gynecology, credited with the vaccine’s initial development, revealed that six years of pilot studies led to the 1980 development of the initial vaccine. He predicted that some form of the sterilizing preparation would reach the medical market by the mid-1990s. 

The vaccine worked, the doctor explained, by attacking and neutering the female pregnancy hormone hCG. The pregnancy hormone, produced shortly after conception, facilitates placental development and the successful implantation of the fertilized egg into the uterine wall. Nothing was mentioned regarding hCG’s link to cancer cell production, membrane electronegativity, and immunological “cloaking.” 

Vaccinating women with a foreign woman’s hCG, researchers learned, prompted a powerful immune response against the natural pregnancy hormone. The end results included sterility, terminated pregnancies, aborted fetuses, and according to the aforementioned data, a greater risk for cancer. 

Promoted for its benefits to “family planning,” this “breakthrough” science represented one of the more coercive methods of population control heralded in the quote by Dr. Paul Ehrlich beginning this chapter. The deployment of this technology is also entirely consistent with the “practical” solutions for “dysgenic populations” advanced by the earliest eugenicists discussed in Chapter 4. 

As reported by the Philippine Medical Association, in the mid-1990s, hundreds of thousands of unsuspecting women began receiving another “experimental” vaccine containing hCG. This time it was said to be for the prevention of tetanus. Later reports confirmed that millions of women in other countries besides the Philippines, including South American nations, Mexico, and America, received a similar hCG contaminated tetanus vaccine. The Philippine Department of Health revealed that almost 20 percent of tetanus vaccines they sampled were positive for the foreign hCG. They did not report on the possible links to increased cancer rates in these women.(HLI, 1995) 

“This study lends credence to what Human Life International (HLI) and some other groups have suspected all along,” said Father Matthew Habiger, president of the international pro-life/family organization. “We first began to hear reports last year about tetanus vaccination campaigns in the developing world that targeted only women of childbearing or pre-child bearing years, and that they required multiple injections. The vaccination program is sponsored by the World Health Organization, an agency with a 20-year history of researching antifertility vaccines,” Fr. Habiger said. “We brought our suspicions to the world’s attention. This new study greatly heightens our concerns.” 

The WHO, and feminist organizations that claimed to care about the health of women, publicly attacked HLI after it called for an investigation into the widespread allegations about the hCG contaminated vaccines. 

The Philippine Medical Association (PMA) reported that nine of the 47 vaccine samples tested were found to contain hCG. They released a letter signed by the three Philippine physicians who actually tested the vaccines. The PMA president attested to the veracity of the letter and the testing process. All the vaccines sampled were taken from various health centers in Luzon and Mindanao. Almost all of them were labeled by one of two Canadian firms, Connaught (Aventis-Pasteur-Hoechst) or Intervax. All the samples were tested with an immunoassay-based method developed by the FDA. 

The tetanus vaccine tested in the Philippines was imported, allegedly, as part of a program against neonatal tetanus sponsored by the WHO. Similar vaccination protocols have also been observed in WHO programs administered in Mexico and Nicaragua, the Philippine Medical Association reported. Tests of the vaccine in Mexico yielded similar results, but none of those tests were performed as part of an actual investigation into the hCG contamination. 

“We view the adulteration of tetanus vaccine with hCG to be a matter of grave concern,” said Fr. Habiger. “It is absolutely essential that any country which has this program in place begin testing the vaccines for contamination.” 

Fr. Habiger suggested that women who received tetanus vaccines be tested for the telltale presence of hCG antibodies in their bloodstream, and that the numbers of miscarriages experienced by vaccinated women be tabulated. 

With the publication of this text, the same may now be said regarding cancers. 

“We strongly suspect something is seriously amiss,” Fr. Habiger complained. “And public confidence in these kinds of vaccination campaigns has been critically eroded in several developing nations. Only an objective, scientifically valid, study of this matter will lay public concerns to rest.” 

A parallel story, written by Suzanne M. Rini, entitled “Open Season on Humanity: Abortion, Contraception, Sterilization, and the Coming Era of Coercion,” appeared in the November, 1995 issue of Celebrate Life.Like many pro-life articles, this too recalled the major affiliations and conflicts of interest between some of the “Pirates of the Sacred Spiral,” and their successful efforts at what appears to be spreading cancer and sterility for population control.(Rini, 1995) 

Closed Electrical Biological Circuits 

If hCG induces cancer cell negativity and immunological suppression, then reversing these electrodynamics may be prudent prevention or cancer treatment. The application of electrical currents into cancerous tissue has been shown to have beneficial effects in many cases of cancer. 

Applying electrodes directly to cancerous tissues, for example, Dr. Björn Nordenström and Dr. Rudolf Pekar pioneered research whereby special platinum needles (electrodes) were inserted directly into tumors.(Nordenström, 1983; Pekar, 1997) This form of therapy became known as electrochemical therapy because it destroyed portions of cancerous tumors by both electrical and chemical means. 

In similar studies, needles were connected to electrical devices that produced direct current. Needles with a positive charge, anodes, and needles with a negative charge, cathodes produced electrical currents. When low voltage (6 to 8 volts) and low micro-amperage (40-80mA) direct currents were administered to tumors, areas around the anodes became highly acidic due to the attraction of negatively charged chloride ions and the formation of hydrochloric acid (pH 1-2). The tumor areas around the cathodes became highly basic (pH 12-14) due to the attraction of positively charged sodium ions and the formation of sodium hydroxide.(Yu-Ling, 1997) Chlorine gas emerged from the skin at entry points of the anodes, and hydrogen gas emerges from the entry points of the cathodes.(Chou et al., 1997) This strong change in pH was one of the factors involved in killing and injuring the tumor cells. So in a sense, direct current stimulation is a form of pH “chemotherapy.” 

According to some investigators, the effectiveness of this type of treatment depends on electrode placement, and dosage of the electrical charge administered in coulombs.(Chou et al., 1997) 

Dr. Yu-Ling reported at the Fourth International Symposium on Biologically Closed Electric Circuits that, by 1997, over seven thousand cases of malignant tumors had been treated in China by this treatment with favorable results.(Yu-Ling, 1997) 

One of Nordenström’s techniques was to place the positive electrode into the tumor and the negative electrode outside of the tumor.(O’Clock, 1997) This resulted in an increased flow of electrons into the tumor, a change in the electrical field around the tumor, and activation of membrane receptors and ion channels. O’Clock’s work also confirmed Ross Adey’s findings that windows of frequency and amplitude exist for tumor cell suppression and proliferation.(O’Clock, 1997) 

Given the above, we believe that devices that create electromagnetic fields, and current flows in the body, may have therapeutic benefits vis-a-vis intracellular and extracellular pH. 

Moreover, with chloride ions principally engaged in tumor-linked acidification, with cancer cells accumulating water, chlorinated water may be seen as an additional risk factor for intracellular acidification, and possible immunological “cloaking” of cancer cells. 

Besides pH changes, the application of direct current to tumor cells has been found to change the membrane potential of tumor cells, alter nutrient uptake by tumor cells, reduce DNA production by tumor cells, and increase immune activity—particularly the attraction of white blood cells to the tumor site.(Chou et al., 1997; Douwes and Szasz, 1997; O’Clock, 1997) 

The application of direct current causes electrolysis, electrophoresis, electroosmosis, and electroporation to occur in tissues creating microenvironmental chemical changes and microelectrical field changes.(Li et al., 1997) 

The chemistry of the microenvironment of healthy cells, injured cells, cancerous cells, and the microelectrical field of these cells are interrelated. Changes in one results in changes in the other. This is easier to remember if you understand that all the chemistry of biological systems involves an exchange of energy. 

Also, all your body cells and tissues are bio electrically interconnected as a primary function of the Sacred Spiral. 

These authors believe this type of electrical treatment of tumors will destroy some cells by electrolysis, and cause other cancer cells to lose their stealth-cloaking-coat of negatively charged glycoproteins, thus enabling the immune system. Loss of this cloaking dynamic, through alterations in pathogenic electrochemistry, enables activation and docking of immune factors and cellular defenses. This includes production of cytokines and interferon and tumor destruction by cytotoxic T-cells and macrophages. As you will read in the next sections, this “cloaking” capability is hardly unique to cancer cells, but is also demonstrated by pathogenic bacteria and immune suppressive viruses that have been associated with malignancies. 

Bacterial Electrodynamics in Cancer 

An interesting phenomenon involves bacteria and viruses that can alter host cell membranes and is associated with certain types of cancer. In the 1950s, Virginia Livingston-Wheeler promoted the idea that cancers are associated with a particular type of pleomorphic bacteria. She named this microbe Progenitor cryptocides (Greek for “the hidden killer”) after she consistently isolated this germ from cancerous tissues.(Livingston-Wheeler and Wheeler, 1977; Livingston-Wheeler and Addeo, 1984; Cantwell, 1990) 

Certain types of bacteria have been known to colonize areas of the body, particularly areas that have compromised blood supply and regional hypoxia. These bacteria naturally produce biofilms as a way of protecting themselves from immunological attack. For example, pseudomonas bacteria can produce a carbohydrate secretion within which they encapsulate themselves.(Straus et al., 1989) These negatively-charged cell coats electrically repulse attacking immune cells. By attaching themselves to human tissue, it is very likely that these bacteria are, likewise, using electrical defenses. 

Some researchers are experimenting with the use of anaerobic bacteria as a form of gene therapy for cancer. When anaerobic bacteria are injected into the body, they tend to accumulate in hypoxic tumor areas. Investigators have advanced their hope of genetically modifying these bacteria to produce anti-malignant proteins as they reproduce.(Lemmon et al., 1997) 

Given the information in this book, the decades of advanced work in genetically modifying infectious microbes is unnerving. Microorganisms are currently being made to: 1) alter the genetic machinery of human cells to which they become attached, promoting the production of certain proteins and hormones; 2) create biofilms around cells altering their surface charge and impacting cell mineral concentrations, cell membrane functions etc; and or 3) secrete their own form of hCG which would change the electrical characteristics of the cells to which they attach. 

It is now well recognized that cancer cells can produce hCG, but certain types of tumor-associated bacteria also produce it.(Backus and Affronti, 1981) When Virginia Livingston-Wheeler reported this same finding back in the early 1970s (Livingston Wheeler and Livingston, 1974) her findings were dismissed and she was labeled a quack. Acevedo and others have repeatedly shown that some tumor-associated bacteria will produce hCG or components of this hormone. 

Acevedo and his colleagues in 1987 did immunocytochemical studies using antisera to hCG, and to its alpha and beta subunits. They demonstrated the expression of hCG-like material in nine bacterial strains. “Seven of these were isolated from patients with cancer and were definitely identified as Streptococcus faecalis (three strains), Staphylococcus haemolyticus (two strains), Staphylococcus epidermidis and Escherichia coli (single strains). The other two strains were cell-wall-deficient (CWD) variants, one identified as Streptococcus bovis isolated from the blood of a patient with a fever of unknown origin and a possible brain abscess.”(Acevedo et al., 1987)  

Fig. 7.6. Electrodynamics of Viral Infections 

Normal cells carry more positive charges on their surface membrane than diseased and cancer cells which turn more superficially negative. This impairs your cells’ electrical defense shield leaving you open to easier infections and genetic invasions. Enzyme therapies may help reduce this risk by helping to remove sialic acid residues from diseased and cancer cells reducing their surface negativity. 

Cancer cell membranes carry distinctive surface proteins that should act as antigens, but they fail to. This is also likely due to the change in membrane surface electrochemistry. Normally, the body would react to foreign invaders and cancer cells by increasing antibody production by B-lymphocytes and increasing production and mobilization of T–cells and macrophages to attack these dangers. However, in cancer, immune cells are blocked from fully acting by compounds secreted by the tumor that inactivate white blood cell body-guards, and by the electrical shield of tumor cells. 

Tumor cells also secrete chemicals and mucoid coats that provide a protective shield of negatively charged molecules around them. The mucoid shield of cancer cells differs very little from the coating on embryonic cells that resist immunological attack.Tumors also release factors that stimulate blood vessels to form and leak plasma into interstitial tissue. This creates lymphatic stagnation and additional disease conditions.

Harmful tumor mucoid coats can be broken down with pancreatic enzymes, bromelain, beta carotene, and heparin, which will chemically and electrically deshield the tumors and allow immune cells to attack.

Virus-to-Cell Membrane Electrodynamics in Cancer 

Coatings of proteins, glycoproteins, and glycolipids encapsulate many viruses. These viral coats may contain either sialic acid or the enzyme sialidase. If sialic acid predominates, the virus will have a negative charge, but if sialidase predominates the virus will have a positive charge.(Cure, 1995) If sialidase predominates, the positively charged virus will be electrically attracted to the negatively charged cell surface. (See figure 7.6) 

An interesting clinical note is that arginine supplementation can activate latent herpes viral infections. Arginine contains a strongly basic guanidine group. It is possible that arginine can enhance the infectivity of certain types of viruses by changing the electrical charge of the virus or cell membranes. It is known that inhibition of the sialidase enzyme will stop the entrance of viruses into cells. This suggests that viral inhibition may occur through chemical measures, or electronic neutralization.(Haltiwanger, 2002) 

More interesting viral errata involves chicken soup—a well known remedy for viral infections of the respiratory tract. When chicken soup is prepared without salt it has been found to contain large amounts of free electrons. These can electrically neutralize viruses with positively charged coats, and prevent viral entry into cells.(Haltiwanger, 2003) 

Electronic microcurrent, infrared, and phototherapy devices, homeopathic preparations, and herbal preparations that supply the body with a plethora of free electrons, also clinically exhibit antiviral activity. 

Treatments that have been reported to disrupt tumor cell coats include pancreatic enzymes,(Acevedo et al., 1998) plant enzymes such as bromelain,(Nieper, 1996) beta-carotene,(Nieper, 1985); heparin,(Nieper at al., 1999) and vaccines against hCG.(Acevedo et al., 1998; Triozzi and Stevens, 1999) 

This latter finding suggests that the World Health Organization’s anti-hCG vaccinations program targeting ethnic and Third World women was likely a depopulation and cancer prevention experiment. 

Polychromatic States and Health: 

A Possible Unifying

Theory Prigonine’s 1967 description of dissipative bioenergy structures advanced a model and an understanding of how open systems, like living organisms that have a steady flow of energy, can self-organize. Clearly, biological systems are designed to take in and utilize energy from chemical sources (e.g., food), but they can also utilize energy and information to maintain their dynamic organization from resonant interactions with electromagnetic fields and acoustical waves. 

According to Dr. Mae-Wan Ho, “Energy flow is of no consequence unless the energy is trapped and stored within the system where it circulates before being dissipated.”(Ho, 1996) This may mean that cellular structures that transduce, store, conduct, and couple energy are critical features of any living organism. 

Living systems are characterized by a complex spectrum of coordinated action and rapid intercommunication between all parts.(Ho, 1996) The ideal complex activity spectrum of a healthy state is polychromatic where all frequencies of stored energy in the spectral range are equally represented and utilized, according to Dr. Ho. In a diseased state, some frequencies may be present in excess and other frequencies may be missing. For example it has been reported that a healthy forest emits a polychromatic spectrum of acoustical frequencies, and an unhealthy forest will have holes in its frequency spectrum. Yet, when the forest regains its health, it again emits a polychromatic spectrum of frequencies. The frequency holes somehow got filled! 

When an area of the body stops properly communicating it will fall back on its own mode of frequency production, which according to Dr. Ho, leads to an impoverishment of its frequency spectrum. In looking at the example of cardiac frequency analyzers it has been discovered that sick people have less heart rate variability than healthy individuals. 

The concept of polychromatism makes sense when you consider phenomena such as the healing effects of: sunlight, full spectrum lights, music, tuning forks, chanting, toning, drumming, crystal bowls, sound therapies, prayer, love, the sound of a loved one’s voice, essential oils, flower essences, healing touch, multiwave oscillators, and homeopathics. Something missing— some frequency or frequencies—are apparently provided by these resonating therapies. 

From the consideration of applied frequency technologies, it can be theorized that one aspect of why these consonant technologies work is because they supply frequencies that are missing in the electromagnetic and acoustical spectra. When missing frequencies are supplied they, in a sense, fill gaps in the frequency spectrum of life. Other technologies might identify frequency excesses and pathogenic frequencies and would provide therapeutic frequency neutralization by phase reversal. 

Electromagnetic technologies such as Rife frequency generators, the Quantum Xrroid Consciousness Interface (QXCI or “QuadMed”), and radionics machines may act similarly by pathogenic frequency phase reversal and neutralization. Royal Rife, a brilliant microscopist, also theorized that equipment using crystal resonant transmissions of energy could cause pathogenic organisms to oscillate to the point of destruction. 

If you consider polychromatism to be the model of the healthy state, then it makes sense that technologies such as electrodermal screening and voice analysis that detect frequency imbalances (excesses and deficiencies) can play potentially beneficial diagnostic roles in health care. 

Therapeutically, we believe doctors will increasingly utilize this type of equipment to treat a broad spectrum of frequency imbalances. More on this subject of therapies that impact the electrodynamics of cells and the future of electromedicine is provided in Chapter 12.

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Advanced Electrogenetics