Learn about package 5:

The ati-Cancer effects of the following nutrients:

L-Glutathione

Enzyme Protocol

ATP

Q10

Introduction To Enzyme Therapy

TumorX Enzymes are able to communicate with the surrounding cells, distinguishing and differentiating between healthy cells and cancerous cells. This distinguishing ability is a key to the TumorX Enzyme Protocol. TumorX Formula 103X, TumorX Formula 303X & TumorX Formula 403X (TumorX Enzymes) are able to destroy cancerous cells piece-by-piece and bit-by-bit. The life saving action begins once a cancerous cell is detected. The very first part of the cell to be destroyed is the fibrin. The fibrin is composed of carbohydrates connected to a protein.

These carbohydrates form a protective canopy that engulfs the cell and allows the cancerous cell to communicate with adjacent cells. Over time as old healthy cells die, a new cell is put into place. If the cancer cell is not destroyed at this point the new un coded cell gets the function code from the cancerous cell, creating a new cancer cell. One of the overwhelming problems is that cancer cells never die on their own. This is why a mechanism based approach like the TumorX Enzyme Protocol has to be implemented.

The photo below describes the outer shell of a cancerous cell.
TumorX Enzymes are able to destroy the cancerous cells.

Pancreatic Enzyme in Clinical Studies
A Simple Explanation

This protective canopy is why Dr. Beard in his 1911 book demonstrated that greater amounts of amolopsyn i.e., TumorX Formula 303X, are need to destroy cancer cells versus what would normally be expected in non-cancerous cells. The Trophoblast Principle of Cancer A key concept underlying the original use of pancreatic enzymes (TumorX Formula 103X and TumorX Formula 303X) for cancer treatment is the trophoblastic theory of cancer. When a human egg is fertilized by sperm, the early cell divisions produce a small ball of cells, which give rise to the blastocyst (pre implantation embryo). The blastocyst possesses a surrounding layer of cells known as the trophoectoderm, which is made of individual cells called trophoblasts. Responsible for protecting the developing blastocyst and for mediating its attachment to the wall of the uterus, trophoblasts create the placenta. During the process of attaching the blastocyst to the uterine wall, trophoblasts express invasive qualities similar to those found in cancer cells. Trophoblasts, however, cease their invasive activity once the placenta is in place and functioning and then differentiate into other cell types. When Scottish embryologist Dr. John Beard first observed the invasive activity of trophoblasts in 1902, he speculated on the similarities between these cells and cancer cells. In addition, he observed that trophoblast invasiveness begins to decline at about the same time that the pancreas in the developing fetus begins to function.

He also theorized that maternal pancreatic enzymes might play a role in containing trophoblastic invasiveness in the uterus. These considerations led to his hypothesis that cancer cells, like trophoblasts, arise from primordial germ cells. Dr. Beard also thought that some of these primordial cells—carrying latent capacities for invading tissues—could escape and spread throughout the body of the developing fetus. He thought it was possible that pancreatic enzymes modulated the degree of trophoblastic invasiveness in the uterus, he suggested that these same enzymes play a role in either limiting or eliminating cancerous cells elsewhere in the body. Dr. Beard worked before the advent of molecular biology and human genetics. Although unable to experimentally establish that pancreatic enzymes had anticancer effects, he published papers and a book about his theory between 1902 and 1911. Other scientists of the time raised significant objections to the trophoblastic theory of cancer, and it was never broadly accepted. The objections were based on the fact the pancreatin enzymes are very large and we not believed to enter into the body through the intestinal wall, and if they were they would be fragment and useless.

Modern Research

Modern research has proven this to be inaccurate. The fact is pancreatic enzyme are detectable in the blood serum. What is known today is that the enzyme attaches to a white blood cell, using it as its locomotive through the body. When an enzyme reaches an area where it is needed it disconnects from the white blood cell and migrates between the cells this is accomplished by the cells vibrating and dividing allowing the enzyme to migrate between the cells. This mechanical action moves the enzymes to areas of the body where no blood vessels are present including the upper layer of the skin tissue. TumorX Protocol asserted, like Dr. Beard, more recently Dr. Kelley and independent researchers like Dr. Gonzales have cured 10's of thousands standing on the shoulders of giants like Dr. Beard and the trophoblasts teaching. Trophoblasts theory and cancer cells have a common origin in primordial germ cells.

We maintained, furthermore, that cancer was initiated when primordial germ cells migrated to a point in the body already weakened by toxic exposure environmental, hormonal system imbalance, and nutritional imbalances are present. At these presumably compromised sites, the germ cells met no opposition from the immune system e.g. enzymes killer T cells etc. and initiated an aggressive invasion of normal tissue, creating malignancy. TumorX treatment approach is based on the belief that primordial germ cells are a major cause of all cancers, no matter where they occur, and that pancreatic enzymes are able to suppress and/or destroy cancers cells, but other nutrients are needed to allow the enzymes to work properly. One needs to keep in mind that enzymes need minerals, co-enzymes, vitamins, nuclides (ATP) and etc. To work properly the fact is when one is deficient in a mineral like magnesium over 300 different enzymatic reactions are not able to properly do their job, this deficiency allows disease such as cancer to destroy the body. When ATP is not found in abundance Cachexia and other nutritional induced diseases will follow, this is simple because the Krebs cycle has been disturbed.

Have more questions now than when you started reading this page? Call the United States technical support office at 229-365-7708 to speak with a TumorX Protocol expert that can answer your questions.

 Fungal Versus Pancreatic Enzymes

The key concept to remember when talking about enzymes is the lock and key mechanism. An enzyme fits with one substrate just like a key fits one lock. There are also mechanical issues to consider with enzymes such as PH issues and size differentials. PH issues are important because you must consider the PH inside the body. The question to ask is, "Will the enzyme function and migrate into the blood stream?" This is why when discussing fungal units they will bring to your attention that they are enteracoated enzymes- which are generally fragile and unable to handle the fluid environment of the human body. Fungal units have not been proven to connect themselves to white blood cells once they have reached the bloodstream like the pancreatic enzymes have proven to do. There is a current inside the vessels due to the pumping action of the heart, so some mechanical locomotion will be accomplished through the action. If relying on blind luck the enzyme will bump or somehow engage fats, cholesterol, fibrin, blood fibrin, protease/glucose proteins and help thin the blood so these functions will occur. This is how the enzymes work vascularly. Keep in mind that an enzyme is not an organism, it does not have a brain, it is a chemical. However, this chemical is able to do thousands of chemical reactions in a very short period of time which makes it remarkable. What has not been demonstrated by the fungal units is the ability to migrate between the cells as the pancreatic enzymes do and effectively destroy cancer cells. One of the main proponents of plant based enzymes- not fungal but plant-based- is Max Gerson. Gerson taught that by not cooking food you would be able to get the enzymes from the plant and repair the body. He also suggested eating materials such as raw beef liver.

He was right, that will greatly increase the nutritional content for the person and in some cases repair their deficiencies so that the natural enzymes already being made in the pancreas will have the substrates to do its job, allowing the body to be repaired. The fungal units (HUT Units): HUT units are hemoglobin units. The assay is determined by how much blood it breaks down in a set time based upon the fact that blood is made of a protein, protease. The completely remarkable thing is that the body has mechanisms in place to protect it and utilize such an interesting enzyme in the body. I would suggest that for simple digestion they are very good. However, for the treatment of cancer, they leave a lot to be desired. One enzyme that is plant based and has been proven to destroy cancer is bromelain. The simplest thing to say about fungal units is that, other than shopping for cost, all of the major promoters of anti-cancer enzymes from the beginning to modern day have all insisted that pancreatic enzymes outperform any other enzyme known. One fact is that the late Dr. William Donald Kelly who was a vegetarian, who taught and promoted vegetarianism only used pancreatic enzymes derived from pigs for his cancer treatment. It has been written by the US Government (cancer.gov) that over 10,000 people went through his protocol. Dr. Kelly would demonstrate with his records that they were in fact cured of cancer. While Dr. Kelly was alive the medical establishment had him arrested, jailed and would not take his records seriously. He was in fact a dentist who cured himself of pancreatic cancer in the 1950's using Dr. Beard's research. While Dr. Kelly was still alive the med student known today as Dr. Gonzalez, formerly of the Sloan Kettering Institute, reviewed his records and is currently undergoing clinical trials using pancreatic enzymes derived from the swine to cure cancer.

Why Glutathione is so important

Glutathione plays important roles in antioxidant defense, nutrient metabolism, and regulation of cellular events including:

• Gene Expression
• DNA and Protein Synthesis
• Cell replication
• Organized Cell Death (apoptosis)
• Controls the action and direction of enzyme function action (first described in 1977 [signal transduction])
• Immune Response
• Helper T cell (cytokine production)
• Killer T cell production (cytokine production)
• Oxidative Stress (protein glutathionylation)

Cancer

• Glutathione plays a role in eliminating many carcinogens/acids and also maintains and optimizes white blood cell function while providing stronger anti-acidic/anti tumor defenses.
  Cancer Letters 57: 91-94, 1991.

Oxidation damage in the body has been demonstrated  to be from glutathione deficiency causing gene expression damage.

Carcinogens are one of the key components in the development of cancer.

    * Glutathione supplementation is helpful when exposed to carcinogenic materials such as the following:

• Tobacco (natural carcinogenic material)
• Benzene (synthetic carcinogenic material)
• Chemo Therapy Drugs (allopathic carcinogenic material)

TumorX L-Glutathione Anti-Carcinogenic Formula will repair the body by taking the toxic materials out of the cells, thus allowing the body to repair itself.

Glutathione is the most abundant active (low-molecular-weight chemical) compound. It is the major antioxidant agent found in human cells.

Human studies demonstrate that adequate protein nutrition is crucial for the maintenance of health. Protein also contains the highest levels of glutathione in the human diet.

TumorX L-Glutathione Anti-Carcinogenic Formula plays important roles in the following: antioxidant defense, nutrient metabolism, and regulation of cellular events including gene expression, DNA and protein synthesis, cell proliferation and apoptosis, signal transduction and immune response.

Understanding free radical biology

Understanding free radical biology is necessary for designing an optimal nutritional countermeasure against sun damage exposure, target radiotherapy, cell cytotoxicity, free radicals (e.g., superoxide, nitric oxide, and hydroxyl radicals) and other reactive species (e.g., hydrogen peroxide, peroxynitrite, and hypochlorous acid) which are produced in the body, primarily as a result of low oxygen metabolism.

Excess amounts of iron and vitamin C can gives rise to the oxidation of biomolecules and cell injury if the body does not contain a healthy amount of anti-oxidants.

Selected  Immune  Cytokines  and  Their  Activities*
Cytokine	Producing   Cell	Target   Cell	Function**
GM-CSF	Th cells	progenitor cells	growth and differentiation of monocytes and DC
IL-1a IL-1b	monocytes macrophages B cells DC	Th cells	co-stimulation
		B cells	maturation and proliferation
		NK cells	activation
		various	inflammation, acute phase response, fever
IL-2	Th1 cells	activated T and B cells, NK cells	growth, proliferation, activation
IL-3	Th cells NK cells	stem cells	growth and differentiation
		mast cells	growth and histamine release
IL-4	Th2 cells	activated B cells	proliferation and differentiation IgG1 and IgE synthesis
		macrophages	MHC Class II
		T cells	proliferation
IL-5	Th2 cells	activated B cells	proliferation and differentiation IgA synthesis
IL-6	monocytes macrophages Th2 cells stromal cells	activated B cells	differentiation into plasma cells
		plasma cells	antibody secretion
		stem cells	differentiation
		various	acute phase response
IL-7	marrow stroma thymus stroma	stem cells	differentiation into progenitor B and T cells
IL-8	macrophages endothelial cells	neutrophils	chemotaxis
IL-10	Th2 cells	macrophages	cytokine production
		B cells	activation
IL-12	macrophages B cells	activated Tc cells	differentiation into CTL (with IL-2)
		NK cells	activation
IFN-a	leukocytes	various	viral replication MHC I expression
IFN-b	fibroblasts	various	viral replication MHC I expression
IFN-g	Th1 cells, Tc cells, NK cells	various	Viral replication
		macrophages	MHC expression
		activated B cells	Ig class switch to IgG2a
		Th2 cells	proliferation
		macrophages	pathogen elimination
MIP-1a	macrophages	monocytes, T cells	chemotaxis
MIP-1b	lymphocytes	monocytes, T cells	chemotaxis
TGF-b	T cells, monocytes	monocytes, macrophages	chemotaxis
		activated macrophages	IL-1 synthesis
		activated B cells	IgA synthesis
		various	proliferation
TNFa	macrophages, mast cells, NK cells	macrophages	CAM and cytokine expression
		tumor cells	cell death
TNF-b	Th1 and Tc cells	phagocytes	phagocytosis, NO production
		tumor cells	cell death

* CTL: cytotoxic T lymphocytes; DC: dendritic cells; GM-CSF: Granulocyte-Monocyte Colony Stimulating Factor; IL: interleukin; IFN: Interferon; TGF: Tumor Growth Factor; TNF: Tumor Necrosis Factor.
** Italicized activities are inhibited.

Your immune system depends on glutathion to destroy and inhibite cancer cells. Other functions of glutathion are destroying virus and other microorganisms.

In order for our bodies to perform its many complex functions, it must be supplied with energy. The demand for energy in the body is increased by numerous factors such as work, exercise and disease. This demand must be met in order to keep our bodies functioning at the optimum level.

The energy-rich chemical compound that provides virtually all the energy needed by our body is known as adenosine triphophate, or simply ATP. The energy released from the breakdown of ATP is used to power all body functions. We need ATP to make our hearts beat, to give our muscles power when we demand it and to maintain our everyday lives. Without adequate ATP stores, we could not walk, run, breathe or even have blood flow through our bodies. So, ATP is considered the "energy currency" of the cell. It is, in fact, the molecule that gives us life.

What is ATP?

Adenosine triphosphate (ATP) is the universal unit of energy used in all living cells. This molecule is produced and broken down in metabolic processes in all living systems. That is to say if you are eating vitamins, minerals or any other food stuff ATP is needed to allow this nutrients to be used in the body to feed the cell, if you suffer from a metabolic disease such as cachexia, fibromyalgia or adrenal fatigue just to name a few, your are ATP deficient.

Energy Currency, the Science of ATP

Known as the ‘energy currency of life,’ ATP can store and transport the energy we need to do just about everything that we do. Essentially all metabolic functions of living cells require energy for operation and obtain it directly from stored ATP. Every cell in the human body produces ATP as part of its metabolic function. In fact 95% of the ATP produced in the body is produced in the mitochondria. For this reason, ATP is often referred to as the power house of the cell, although ATP has several other equally important functions as well.

All molecules contain energy, stored in the molecular structure itself. A portion of that energy can be used to do work. This is called free energy.

Oxidation of a molecule results in the release of free energy. Complete combustion (burning) of organic molecules, eg, releases all of the available free energy as heat. Reduction of a molecule requires an input of energy.

Energy can be transferred from one molecule to another by enzymes. The molecules that are converted by enzymes, that is, the reactants, are called substrates.

Nutrients are organic molecules that are ultimately derived from food sources. They start off as fats, carbohydrates, and proteins. Enzymes such as pancreatic enzymes example in intermediate metabolism oxidize nutrient molecules to a form that can be converted to energy by mitochondria. Fats, carbohydrates and proteins are broken down to individual fatty acids, simple sugars and amino acids.

Phosphate Groups and Energy?

These molecules can transport energy because phosphate bonds contain a lot of potential energy, which is released when they are broken. Energy is stored in the covalent bonds between phosphates, with the greatest amount of energy. Humans /mammals Eat Energy Originally Obtained by Plants and such Humans, cannot make organic compounds from inorganic sources. We must obtain useful compounds from organic sources by consuming plants and animals ect.

How Is ATP Actually Made?

ATP is produced by humans during a catabolic process known as cellular respiration. Because of this fact one would believe we could never become deficient in ATP, but this is not true, and when this deficiency occurs a cascade of problems will be evident Cachexia in late stage cancer patients, heart issues, just to name a few. Cellular Respiration In cellular respiration food molecules are broken down and the released energy is transformed into ATP. Organisms catabolize (break down) carbohydrates, most commonly glucose, to ultimately make ATP and use if for anabolic cellular reactions. Glucose catabolized by through the processes of aerobic respiration and anaerobic fermentation. Aerobic respiration utilizes glycolysis, synthesis of acetyl-CoA, Krebs cycle, and electron transport chain; the end result being the complete breakdown of glucose into carbon dioxide and water. Through these catabolic reactions up to 34 molecules of ATP can be made from every molecule of glucose. Oxygen is a vital component of this highly efficient process, hence the name ‘aerobic respiration’

Where Is ATP Made?

In eukaryotic cells, complex cells that possess a nucleus, ATP is synthesized in the tiny energy factories called mitochondria.

Co-Enzyme Q10 (CoQ10) is a compound found naturally in the energy-producing center of the cell known as the mitochondria. Co-Enzyme Q10 is involved in the making of an important molecule known as adenosine triphosphate (ATP). ATP serves as the cell's major energy source and drives a number of biological processes including muscle contraction and the production of protein. Co-Enzyme Q10 also works as an antioxidant.

TumorX BioEnerGenics Co-Enzyme Q10

Co-Enzyme Q10: Squamous cell carcinoma can be reversed and cured using this natural substance. In fact, a deficiency induces cancer and allows viruses that promote cancer inside the human body to go unchecked! 2 Co-Enzyme Q10 is Dose Dependent...1 * Ninety mg of Co-Enzyme Q10 was administered daily for 3 months, 6 of 32 patients had partial cancer regression. * When 300 & 390 mg of Co-Enzyme Q10 were given daily for 4 months, 2 of 2 patients had complete cancer regression. *

In other studies, a 49-year-old patient had complete disappearance of lung-area tumor after 6 months of daily doses of 390mg Co-Enzyme Q10. * A 75-year-old patient had complete remission with no metastasis of single breast cancer after lumpectomy and taking 390 mg Co-Enzyme Q10 daily for 4 months. From our experience, 500-1000mg daily is the ideal dosage to destroy cancer cells inside the human body. The article below discusses the correlation between viruses and cancers as well as how TumorX BioEnerGenics Co-Enzyme Q10 can help you prevent and/or cure cancer in your body. 2

The National Cancer Institute on the Effectiveness of Co-Q10...1 A study conducted in Denmark followed 32 breast cancer patients for 18 months. The disease in these patients had metastasized to other areas of the body. The patients received Co-Q10 in addition to standard therapy. The survival rate of these patients was 100%. Six were shown to have evidence of remission, none of the six showed further signs of metastasis. One of the 6 patients and a new patient were treated for several months with higher doses of Co-Q10. Surgical removal of the primary breast tumor had been performed in these patients with residual cancer cells still remaining. After 3 to 4 months of supplementation with Co-Q10, both patients experienced complete regression of residual breast tumors. All 32 patients from the original study were alive at 24 months of observation. This same report also states evidence that coenzyme Q10 lengthens the survival of patients with pancreatic, lung, rectal, laryngeal, colon, and prostate cancers (this information also exist in peer-reviewed, scientific literature).

Cancer needlessly claims the lives of about 560,000 americans each year!1 This article explores the use of TumorX™ BioEnerGetics CoQ-10™, an immune stimulant that has been proven to defeat cancers.

My intent is to educate, inspire, and show unprecedented hope to you and your loved ones. When the immune system is compromised, gene damaging viruses are able to invade the DNA of healthy cells, thus creating cancerous cells.

Viruses Attack DNA

One largely unspoken cause of cancer is viral related. Viruses attack DNA, which cause the immune system to weaken, thus resulting in different types of cancer.3 Breast4 and prostate5 cancer, two of the most prevalent cancers, are two examples of viral related cancers. In a study of human breast cancer, 38.5% of the cancerous tissues examined contained a rodent-transmitted virus:3 mouse mammary tumor virus.

Viruses have contributed to the world-wide cancer epidemic. Aging and malnutrition weaken the body’s immune system and consequently leave the body vulnerable to harmful viruses. In the U.S., 77% of all cancer patients are 55 years and older.1 As of 2007, there were over 186,000 cases of cancer resulting from malnutrition, and the rates continue to grow!1

Some known viruses that cause cancer include: hepatitis B virus (HBV),1 human immunodeficiency virus (HIV),1 human papilloma virus (HPV),1 and heli­cobacter pylori (H. pylori).1 Studies have shown that 75% of liver cancer is caused by Hepatitis B or C.4 The Epstein Barr virus (EBV) infects more than 90% of the world population.9 EBV has been linked to: breast cancer, gastric cancer, nasopharyngeal carcinoma, lymphomas, Hodgkin’s disease/lymphoma, Non-Hodgkin’s lymphomas, and African Burkitt’s lymphoma.2,9

The fundamental difference between cancerous and non-cancerous cells is that cancerous cells do not respond to adjacent cell commands.6 Cancer is a metabolic parasite which destroys the body’s bio-energy6 and invades functioning organs. BioEnerGetics Q-10™ promotes the body’s creation of bio-energy by rebuilding and repairing the immune system. Co-Enzyme Q10 is required in all human cells, in fact, low blood levels of Co-Enzyme Q10 have been detected in patients with cancer.13

Healthy Immune System Cures Cancer

A study reviewed the relation of Co-Enzyme Q10 to the regression of breast cancer.7,10 When 90 mg of Co-Enzyme Q10 was administered daily for 3 months, 6 of 32 patients had partial cancer regression.7,10 When 300 & 390 mg of Co-Enzyme Q10 were given daily for 4 months, 2 of 2 patients had complete cancer regression.7,10 In other studies, a 49-year-old patient had complete disappearance of lung-area tumor after 6 months of daily doses of 390mg Co-Enzyme Q10.8,10 A 75-year-old patient had complete remission with no metastases of single breast cancer after lumpectomy and taking 390 mg Co-Enzyme Q10 daily8 for 4 months.

The National Cancer Institute peer-reviewed studies & anecdotal evidence10 and reported that patients who supplemented with Co-Q10 outlive the statistical mortality rate for patients with pancreatic, lung, rectal, laryngeal, colon, and prostate cancers.10