Cancer and ATP: The Photon Energy Pathway

Readers' Comments

Professor Bruce Ponder of the University of Cambridge led a study that has opened up the field of chromosomal aberrations and screeming mutated genes that increase the risk of developing cance by up to 60 (NST Tuesday, May 29, 2007, p 27)

The success of the research is its ability to scan large stretches of the human genome through a new technique to assess 200,000 blocks of DNA simultaneously instead of one by one. While that research study concentrated on genes associated with breast cancer the same technique can used in patients with other forms of cancers. The technique speeds up the rate of gene identification, especially mutated genes for a range of cancers and it helps to calculate a woman\'s predisposition to develop breast cancers over a lifetime.

Certainly, it is am important discovery and all the more important when it is properly understood in terms of preventive medicine. Firstly, there is need to understand what causes genetic mutation and chromosomal aberrations, not just the mechanisms involved but the damage initiated at the molecular and submolecular level. It is clear that while secondary free radicals such as the peroxynitrite radical tends to cause oxidative damage to cell membranes the hydroxyl radical, produced by the reaction between the superoxide and hydrogen peroxide produced during cell metabolism can oxidatively damage the DNA molecule by attacking the hydrogen bonds. Enzymes involved in the replication of genetic material can also be oxidatively damaged by oxidative stress produced by both the peroxynitrite and hydroxyl radicals.

So, the first point to note is that people with genetic mutations have had their genetic material esposed, at some point, to excess free radicals or chemical stressors or drugs that generate free radicals in the body.

Excess superoxide in the cytoplasm, on the other tends to raise the acidity that shuts down the antioxidant enzyme system involved in the Kreb\'s cycle and that can favour the rerouting of the glucose molecule through another pathway that yields alcohol as the energy molecule of the cell. As there is no ATP produced the cell resorts the alcohol breakdown for its energy and that effectively transforn it into a cancer cell.

Hence, strictly speaking, it is not the genes or mutated genes that cause cancer. The real cause is biochemical in nature that depends very much on the free radical-antioxidant equilibrium wherein excess free radicals lead to oxidative stress and oxidative damage. Mutated genes and chromosomal aberrations, do not by them selves cause the formation of cancer cells but indeed when these are present, the risk of developing cancers increases and quite rightly, there is no direct link but it serves as aclue to predisposition to cancers.

There are studies that have documented a relatively high population of free radicals in people with trisomy-21 and other similar aberrations. Also, diabetics whose blood sugar levels are high also have relatively higher populations of free radicals in their body quite similar to obese people as free radical scavenging activity in fatty tissue is much slower that in the watery medium. Hence reducing abdominal girth as a way to reduce visceral fat tends ti improve blood chemistry and reduces risk to cancers. Another recent study clearly indicated that diabetics have a incidence in fertility problems and risk damage to membranes and the DNA in spermatozoa.

At the biochemical level, how is this clue to a predisposition to cancers explained? Well, normal and undamaged genes produce normal biomolecules that are neutral or they may produce antioxidant molecules. Some types of damage to the genetic material may slow down cell division but some types of damage in mutated genes may produce abnormal molecules that act like free radicals and can initiate free radical chain reactions or produce localised damage to cell membranes and aid the accumulation of the superoxide in the cytoplasm by depleting the antioxidant enzymes within the cell or imparing the MT protein system in the mitochondria.

From this perspective, the scanning test devised by the Cambridge research team has wide implications in routine scanning for preventive medicine. Once the predisposition has been identified, a diet that ensures a high intake on natural antioxidants and the elimination of trans-fatty acids and TOFU and long-chain fatty acids, elimination of ciggarettes and alcohol and elimination of food with synthetic presevatives and syhthetic vitamins will naturally reduce the risk of developing cancers.

BELDEU SINGH
(copyright: porixbiotech sdn bhd)

Posted by: BELDEU SINGH on June 3, 2007 10:46 PM

 

Thanks for this great article, Sepp!

Kremer\'s Photon Switch article will be in the August/September issue of the Townsend Letter.

Posted by: David Lowenfels on June 7, 2007 02:25 PM

 

This is one of the most significant articles I\'ve ever seen posted here. Your efforts to bring new, exciting and credible information is much appreciated.

Posted by: Sharry Edwards on June 10, 2007 10:32 AM

 

read once were the cells can take only so much abuse (toxin exposure) before going to fermantation ...once getting to the 100 mark their was no going back ...is this thinking still hold true (can nature repair itself)

Posted by: darrell dixon on July 22, 2007 04:39 PM

 

CHROMOTHERAPY IN CANCER and "STRANNIK SYSTEM" Dear Professor, I want to promote energy assessment by Energo-Electro-Photography(Virtual Scanning-"STRANNIK") in cancer and generally become a diagnostic method, and rebalance energy irradiation with light color (color therapy). Please join me in this research proposal, as leader, because I can not go alone. The basic idea of this theory is that the oxidation of hydrogen and carbon atoms, arising from the degradation of carbohydrates, is by two distinct processes based on oxidation-reduction electron transfer and photochemical process of energy release on the basis of color complementary, predominance of one or another depending on intracellular acid-base balance. Final biological oxidation, the production of CO2 and H2O, should be reconsidered in the sense that a distinction must be made between the oxidation of carbon and hydrogen oxidation. In the case of carbon atoms, cytochrome oxidase must have an alkaline chemical structure, to be colored green and so can absorb additional red energy carbon atoms derived from carbohydrate. For the oxidation of H atom cytochrome oxidase must have a acidic chemical structure, to be colored red, and so can absorb additional green energy hydrogen atom derived from carbohydrate. We propose an experiment to prove that the final biological oxidation, in addition to its oxidation-reduction, with formation of H2O and CO2,there is a photochemical effect, by which energy is transferred from the H atom, or C, process is done selct, the colors, complementary colors on the basis of the structures involved are colored (red hemoglobin Fe, Mg chlorophyll green, blue ceruloplasmin Cu, Fe cytochrome oxidase red, green cytochrome oxidase with Cu etc.). The basic idea is that if life pigments (chlorophyll, hemoglobin, cytochromes), which provides energy metabolism of the cell, are colored, we can control their activities through chromotherapy, on the basis of complementary color and energy rebalance the body, with a figured COLOR ELECTROPHOTOGRAPHY. In my opinion, at the basis of malign transformation is a disturbance of energetical metabolism, which reached a level that cell can not correct (after having succeeded before, many times), disturbance that affects the whole body in different degrees and requires corection from outside starting from the ideea that the final biological oxidizing takes place through photochemical process with releasing and receieving energy. I SUGGEST TO YOU AN EXPERIMENT: TWO PLANTS, A RED (RED CORAL) LIGHT ONLY, IN BASIC MEDIUM, WITH ADDED COPPER, WILL GROW, FLOWER AND FRUIT WILL SHORT TIME, AND THE OTHER ONLY BLUE-GREEN LIGHT(TOURQUOISE), IN AN ACID MEDIUM, WITH ADDED COPPER CHELATOR , WHICH GROWS THROUGHOUT WILL NOT GROW FLOWERS AND FRUIT WILL DO. CULTURE OF NEOPLASTIC TISSUE, IRRADIATED WITH MONOCHROMATIC BLUE-GREEN (TOURQUOISE) LIGHT, IN AN ALKALINE MEDIUM, WITH ADDED COPPER, WILL IN REGRESSION OF THE TISSUE CULTURE. CULTURE OF NEOPLASTIC TISSUE, IRRADIATED WITH RED (RED CORAL) LIGHT, IN AN ACID MEDIUM, WITH ADDED COPPER CHELATOR, WILL LEAD TO EXAGERATED AND ANARCHICAL MULTIPLICATION. If in photosynthesis is the direct effect of monochromatic irradiation, in the final biological oxidation effect is reversed. Exogenous irradiation with green, induces endogenous irradiation with red, and vice versa. "About Carcinogenesis." Final biological oxidation, the production of CO2 and H2O, should be reconsidered in the sense that a distinction must be made between the oxidation of carbon and hydrogen oxidation. In the case of carbon atoms, cytochrome oxidase must have an alkaline chemical structure, to be colored green and so can absorb additional red energy carbon atoms derived from carbohydrate. For the oxidation of H atom cytochrome oxidase must have a acidic chemical structure, to be colored red, and so can absorb additional green energy hydrogen atom derived fromcarbohydrate.In my opinion, at the basis of malign transformation is a disturbance of energeticalmetabolism, which reached a level that cell can not correct (after having succeeded before, many times), disturbance that affects the whole body in different degrees and requires corection from outside starting from the ideea that the final biological oxidizing takes place through photochemical process with releasing and receieving energy. "Duality of cytochrome oxidase. Proliferation (growth) and Differentiation (maturation) cell." Cytochrome oxidase is present in two forms, depending on the context of acid-base internal environment : 1.- Form acidic (acidosis), which contains two Iron atoms, will be red, will absorb the additional green energy of the hydrogen atom, derived from carbohydrates, with formation of H2O, metabolic context that will promote cell proliferation. 2.-Form alkaline(alkalosis), containing two Copper atoms, will be green, will absorb the additional red energy of the carbon atom, derived from carbohydrates, with formation of CO2, metabolic context that will promote cell differentiation. It is known that in conditions of acidosis (oxidative potential), the principle electronegativity metals, Copper is removed from combinations of the Iron. So cytochrome oxidase will contain two atoms of iron instead of copper atoms, which changes its oxidation-reduction potential, but (most important), and color, which radically change its absorption spectrum, based on the principle of complementary colors. According to the principle electronegativity metals, under certain conditions the acid-base imbalance (acidosis), iron will replace copper in combination,leading to changing oxidation-reduction potential, BUT THE COLOR FROM GREEN, TO REED, to block the final biological oxidation and the appearance of aerobic glycolysis. In the final biological oxidation, in addition to an oxidation-reduction process takes place and a photo-chemical process,based on complementary colors, the first in the electron transfer, the second in the energy transfer. A body with cancer disease will become chemically color "red"(Acid, as evidenced by laboratory), and in terms of energy, "green"(visible by color Electrophotography ;VIRTUAL SCANNING). A healthy body will become chemically color"green"(Alkaline,as evidenced by laboratory) and in terms of energy, "red" (visible by Electrophotography ; VIRTUAL SCANNING). (Green body) with alkaline chemical structure, with energy connection type C = O, and red energy , from the oxidation of the carbon energy C = O derived from carboxylic acids. (Red body) with acid chemical structure, with connections Carbon non-energy C-OH, (non-energy, phenolic acids, with strong oxidizing, prone to multiplication), and green energy , which comes from oxidation of hydrogen atoms derived from carbohydrates). Carbon Energy O ::C:: O; Non-Energy Carbon :O: C :O: I want to promote energy assessment by Energo-Electro-Photography(STRANNIK VIRTUAL SCANNING) in cancer and generally become a diagnostic method, and rebalance energy irradiation with light color (color therapy). Please support me in this research, as leader of the project and scientific coordinator. This process is carried out based on complementary colors, which are coenzymes oxidative dehydrogenation and oxidative decarboxylation is colored . It reveals the importance of acid-base balance, the predominance of the acidic or basic, as an acid structure (red), not only can gain energy from the carbon atom red (the principle of complementarity), but can not assimilate (under the same principle). It must therefore acid-base balance of internal environment, and alkalinization his intake of organic substances by the electron donor. By alkalinization (addition of electrons) will occur neutralize acid structures, the red, they become leucoderivat, colorless, and inactive, while the basic, which because of acidosis became neutral, colorless and inactive, will be alkaline in electron contribution, will be in green, and will absorb red energy from the carbon atom. So, on two kinds of vital energy, it is clear correlation between the chemical structure of the cell (body),and type of energy that can produce and use. Thus a cell with acidic chemical structure, can produce only energy by oxidative dehydrogenation (green energy), because the acid can only be active coenzymes with acid chemical structure, red, will absorb the complementarity only green energy of hydrogen. Basic structures which should absorb red energy from carbon , are inactive due to acid environment, which in turn chemically in leucoderivat, so colorless structures, inactive. Conversion of these structures to normal, operation by alkalinization could be a long lasting process, therefore, we use parallel chromotherapy, based on the fact that these COENZYMES INVOLVED IN BIOLOGICAL OXIDATION FINALS ARE COLORED AND PHOTOSENSITIVE. If we can determine the absorption spectrum at different levels, we can control energy metabolism by chromotherapy - EXOGENOUS MONOCHROMATIC IRRADIATION . Energy absorption in biological oxidation process itself, based on complementary colors, the structures involved (cytochromes), is the nature of porphyrins, in combination with a metal becomes colored, will absorb the complementary color, corresponding to a specific absorption spectrum, it will be in - ENDOGENOUS MONOCHROMATIC IRRADIATION. This entitles us to believe that: In photosynthesis,light absorption and its storage form of carbohydrates, are selected,the colors, as in cellular energy metabolism, absorption of energy bythe degradation of carbohydrates, is also done selectively, based on complementary colors. Thus, exogenous irradiation with monochromatic green will neutralize, by complementarity, coenzymes red, acidic. In will reactivate alkaline coenzymes, which have become due acidosis leucoderivat, so colorless and inactive. Without producing CO2, carbonic anhydrase can not form H2CO3, severable and thus transferred through mitochondrial membrane. Will accumulate in the respiratory Flavin, OH groups, leading to excessive hydroxylation, followed by consecutive inclusion of amino (NH2). It is thus an imbalance between the hydrogenation-carboxylation and hydroxylation-amination, in favor of the latter. This will predominate AMINATION and HYDROXYLATION at the expense CARBOXYLATION and HYDROGENATION, leading to CONVERSION OF STRUCTURAL PROTEINS IN NUCLEIC ACIDS. Meanwhile, after chemical criteria, not genetic, it synthesizes the remaining unoxidized carbon atoms, nucleic bases "de novo" by the same process of hydroxylation- amination,leading to THE SYNTHESIS OF NUCLEIC ACIDS "DE NOVO". Please get involved in this project as a scientific leader. Sincerely yours, Dr.Viorel Bungau Romania Libertatii 22 Cristian 507055 Brasov

Posted by: Viorel Bungau on March 23, 2016 10:55 AM

 

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