How to use TumorX Apoptosis Protocol
"How To Properly Implement the TumorX Protocol "
One of the Strongest Anti-Cancer Packages
Each Bottle Contains Different Unit Count
& milligrams per capsule, click on the tab to see information.
- Side Effects
Pancreatic and Plant Enzymes, Apoptosis Easy Digest Bloodroot and Apoptosis Easy Digest, Apoptosis Full Strength, ATP & Q10
Protocol Package 6
The combination of enzymes, Apoptosis Protocol, ATPand Q10 is an excellent combination of nutrients:
- Enzymes (Formual 103X, 303X and 403X)
- Detoxify The Body
- Kill cancer cells
- Improve the condition of the blood
- Help digest food thus decreasing the risk of starvation
- Apoptosis Easy Digest Bloodroot
- Kills Cancer Cells
- Removes the ability of cancer cells to hide from the immune system
- Kills microorganisms
- Easy on the stomach- less side effects compared to Apoptosis Full Strength Bloodroot.
- Apoptosis Full Strength Bloodroot
- Kills Cancer Cells
- Removes the ability of cancer cells to hide form the immune system
- Kills microorganisms
- Induces Killer T cells
- Induces Helper T Cells
- Feeds the mitochondria
- Helps the cells produce ATP
- Increases macrophages
- Helps protect the heart and other vital organs from chemo drugs.
- Using the liver, ATP Converts lactic acid into energy
- Increases blood flow and oxygen to organs, converting the body from anaerobic to aerobic
- Kills cancer cells
This package will not only kill cancer cells, using four different mechanisms, but will also help detoxify and repair the body.
||TumorX Formula 103X: 2 bottles containing 180 capsules, 1000mg capsules per bottle
||TumorX Formula 303X: 1 bottle contains 720 capsules, 1000 mg capsules
||TumorX Formula 403X: 1 bottle contains 180 capsules, 1000 mg capsules
||TumorX Formula Apoptosis Easy Digest: 1 bottle contains 540 capsules, 350 mg capsules
||TumorX Formula Apoptosis Full Strength: 1 bottle contains 90 capsules, 350 mg capsules
||TumorX Formula ATP: 1 bottle contains 360 capsules, 350 mg capsules
||TumorX Co-Q10: 1 bottle contains 60 capsules, 250 mg capsules
This product is pure nutrition; no fillers, additives or synthetic chemicals.
The gelatin capsule complies with the requirements published in:
The United States Pharmacopoeia (USP); XXIV / National Formulary (NF) 19
The European Pharmacopoeia (EP); 3rd Edition
Kosher and Halal certified
This is a simplifed vershion of the directions for a better understanding one should read the booklets:
How to use Tumorx Apoptosis Protocol package 6... Click Here
Suggested times for Taking Enzymes and Eating
ATP can be taken any time during the day, with or without food. ATP and CoQ
10 work synergistically when taken together.
Get up at 7 a.m.
Breakfast Eat at Approx. 8 a.m.
- 403X Take 2 capsules
- ATP Formula 4 capsules
- Bloodroot easy Digest Formula Take 1 capsule( see paper)*
10 Take 1 capsule
After meal 9:30 a.m.
12 Noon.Lunch Eat at Approx.
- 403X Take 2 capsules
- ATP Formula Take 4 capsules
- Bloodroot Easy Digest Formula Take 2 capsules*
1:30 p.m. After meal
5 p.m.Supper Eat at
- 403X Take 2 capsules
- ATP Formula Take 4 capsules
- Bloodroot Easy Digest Formula take 3 capsules
- CoQ 10 Take 1 capsule
6:30.p.m. After meal
8:30 p.m. 1 hour before bed
No Side effects in most cases.
Diarrhea, constipation, abdominal pain/cramps, nausea, or vomiting may occur.
Side effects normally do not occur.
If one does not take the product correctly one can expect:
Nausea, vomiting, projectile vomiting, and hypertension could occur.
If one has any advere reaction in all likely hood it is created by the bloodroot in the Apoptosis Protocol, one needs to follow the directions to mitigate any possable adverse reactions.
How to use Tumorx Apoptosis Protocol ... Click Here
ATP Pure Energy
ATP is not a stimulant and no side effects have ever been determined when involved in clinical studies.
No side effects in the majority of cases.
Occasional stomach upset, increased energy when taken late in evening, one should consume before 1:00PM
TumorX Package 6 Formulation Strategy:
Pancreatic & Plant enzymes (Formula 103X, 303X and 403X), Apoptosis Easy Digest, Apoptos Full Strength, ATP & Q10
The combination of Apoptosis Easy Digest and Apoptosis Full strength, Formula 103X, Formula 303X Formula 403X, Q10 and ATP are excellent combination of nutrients. Formula 103X helps to detoxify the body and helps to remove human chorionic gonadotropin (hCG)… this is the hormone the cancer produces to hide itself from the immune system, that is to say hCG cloaks the cancer cells from the immune system. Because Formula 103X is a natural mixture of pancreatic enzymes, it has the ability to convert dead cells into food. The waste byproducts will then leave through the waste system. The process of dead cells being recycled inside the human body is completely natural.
TumorX Package 6 versus TumorX Package 5
TumorX Package 6 is very similar to TumorX Package 5. Package 5 uses L-glutathione to detoxify the body and stimulate immune system to help kill cancer cells. Package 6 uses Apoptosis Easy Digest and Apoptosis Full Strength so all the cancer cell can experience the ability to self-destruct.
Apoptosis Easy Digest and Apoptosis full strength both uses the herb bloodroot (Sanguinaria Canadensis) which contain the dietary agent’s active ingredient Sanguinarine and chelerythrine that induce self-destruction of cancer cells. Bloodroot has been successfully used for over 300 years. Studies demonstrate that sanguinarine and chelerythrine induce apoptosis in cancer cells including: epidermoid carcinoma, prostate cancer, breast cancer, endocervical (cervix), melanoma, colon adenocarcinoma, lung non-small cell carcinoma, uveal melanoma (eye cancer), Non-Hodgkin's lymphoma, Acute myeloid leukemia (AML), erythroleukemia, neuroblastoma, and colon carcinoma to name a few. Historically Sanguinarine and chelerythrine have been known to kill all types of cancer cell. To date all cancer cells tested with Sanguinarine and chelerythrine have yielded positive results.
TumorX Package #6 Components
Formula 103X helps to detoxify the body and helps to remove human chorionic gonadotropin (hCG). The cancer produces this hormone to hide itself from the immune system, that is to say hCG cloaks the cancer cells from the immune system. Because Formula 103X is a natural mixture of pancreatic trypsin, chymotrypsin, elastase, carboxypeptidase A1, A2, and carboypeptidase B, it has the ability to convert dead cells into food, then the waste byproducts will leave through the waste system. The process of dead cells being recycled inside the human body is completely natural.
Formula 303X is a specialized enzyme that helps balance the body by removing excess carbohydrate chain from cancer cells. This action takes place as the enzymes are destroying the cancer and post mortem, allowing the waste product to quickly and efficiently be removed from the body. This quick action helps to prevent the dead cells from causing fermentation, causing unneeded stress on the system as a whole; one could easily say that this process helps to kill cancer cells while detoxification takes place.
Formula 403X is a proteolytic digestive enzyme called bromelain. Bromelain contains high concentrations of sulfur. Organic sulfur is a natural agent to remove heavy metals from the body. Formula 403X has demonstrated excellent anti-inflammatory properties. Formula 403X helps digest protein, allowing the other anticancer enzymes the body produces to go into the bloodstream and fight the cancer cells. Additionally, Formula 403X helps stop the formation of platelet aggregation and rouleaux. these processes are prior to a blood clotting, Rouleaux formation can be very troublesome and can create a low oxygen environment which hinders the evacuation of gases from the body.
The anti-cancer properties of bromelain cannot be overstated. Bromelain has shown to e beneficial in regulating tumor growth and its metastasis. Batkin et al 1995, Honne 1983; Sato et al 1993, who were esearchers at the Queensland Institute of Medical Research showed that two proteins found in bromelaine named CCS and CCZ were found to block growth of tumor cells including breast, lung, colon, ovarian, and melanoma. These malignancies represent about 30% of all cancers.
ATP Pure Energy Research funded by the Department of Veterans Affairs and the American Liver Foundation, found that cachexia is metabolic starvation that triggers conservation mode- a process that stops the production of stomach acid, intrinsic factor, pepsinogen, pancreatic enzymes and bile. This condition is common at the end stages of the disease process. Cachexia produces extreme pain when eating is attempted and constant pain the rest of the time.
It is estimated that 80% of patients with upper gastrointestinal cancer and 60% of patients with lung cancer develop cachexia before diagnosis of their cancer. In reality these patients are not cachexic, but are rather at the beginning of the starvation mode that will become cachexia if not reversed by nutrition. The dire fact is that cachexia is not reversible unless one uses ATP to convert the lactic acid back into glucose. One of the problems is the net loss of four molecules of phosphate per conversion, creating a net deficiency of ATP in the body. Now keep in mind that Q10 is the one of the precursors for ATP, and that ATP is recycled in the body. We basically need to restart the digestion process by allowing nutrients to enter into the body, feeding the cells and allowing an increase in metabolism thus increasing ATP production and reversing the starvation.
Package 6 is for cancer patients with cancer/metastasis to liver or lung who have already experienced significant weight loss in the form of starvation but who are not typically cachexic before diagnosis of cancer. For patients who are simply nutritionally starved, one of my goals in this formulation was to stop the process of starvation and cachexia before it compromised their immune and endocrine systems, before it caused the body’s inability to repair. Using the healthy liver, ATP Converts lactic acid into energy/glucose, increases blood flow and oxygen to organs, and converts the body from anaerobic to aerobic- a process which kills cancer cells.
Coenzyme Q10 BioEnergenic Formula, or simple Q10, is also used in this package. Q10 induces macrophages killer T and helper T cells. These cells have the ability to kill cancer cells as long as they are not cloaked by hCG. Pancreatic enzymes, however, remove hCG from the blood stream and Q10 allows the pancreatic enzymes to last longer in the body without degrading the enzymes, plus speeds up their chemical actions producing synergy between them. Q10 acts as fuel to feed the mitochondria and acts as a precursor to ATP, which is the energy source or chemical energy for the body. An example of this would be the "sodium-potassium pump," this action balance the pH of the cells.
Please keep in mind that when Q10 is deficient, by default ATP could be deficient. These deficiencies decrease the body’s pH and make and acidic environment- making a hostile environment for healthy cells and a breeding ground for cancer cells.
Apoptosis Easy Digest and Apoptosis Full Strerenght Formulas treatment was found to result in a dose-dependent decrease in the viability of cancer cells. Normally, cancerous cells are unable to experience apoptosis by natural means. DNA (deoxyribonucleic acid) ladder assay demonstrated that, compared to vehicle-treated control, Tumorx Apoptosis Formulas treatment of squamous cell carcinoma resulted in an induction of programmed cell death as signaled by the nuclei in functioning cells.
This process is characterized by cleavage of the DNA into fragments that give a so called laddering pattern when the solid phase of the cell liquefies.
The induction of apoptosis by Tumorx Apoptosis Formulas was also especially clear when viewed with confocal microscopy (this microscope allows the observer to visualize objects in a single plane of focus, thereby creating a sharper image). This method identified the necrotic squamous cell carcinoma.
TumorX Apoptosis Formula &
DNA Cell Cycle Analysis
The DNA cell cycle analysis showed that sanguinarine treatment did not significantly affect the distribution of cells among the different phases of the cell cycle in squamous cell carcinoma. This is especially important because this proves definitely that Tumorx Apoptosis Formulas will not harm the DNA of cells. The research proves that Tumorx Apoptosis Formulas are effective anticancer formulas.
Agents that can eliminate the cancerous cells via a programmed cell death but do not affect the normal cells have a therapeutic advantage for the elimination of cancer cells. In contrast, TumorX Apoptosis Formulas will not harm the patient like synthetic allopathic drugs do.
Studies have shown that Tumorx Apoptosis Formulas are an inhibitor of the activation of nuclear transcription factor NF-B, which has been implicated to play a key role in the regulation of cell growth, cell cycle regulation, and apoptosis. The anti-tumor properties of Tumorx Apoptosis Formulas are constantly being reestablished.
Studies provide more definitive evidence that Tumorx Apoptosis Formulas at micromolar concentrations impart a cell growth-inhibitory response in human cancer cells via an induction of apoptosis.
Safety of TumorX Apoptosis Formulas
The concerns related to herbs with emetic potential are of primary significance when patients do not follow the TumorX Apoptosis Protocol...Click Here
When using Apoptosis Formulas one should follow and understand the TumorX Protocols.
Chelerythrine and Sanguinarine
Apoptosis Easy Digest contains slippery elm to aid the digestive track by calming and soothing as it comes in contact with potential irritants found in the small and large intestine. Bloodroot (Sanguinaria canadensis) contains two key anticancer phytochemicals sanguinarine and chelerythrine.
Sanguinarine and chelerythrine induce apoptosis, the self-destruction of cancer cells. These components also stop the cancer from receiving nutrients by destroying the blood supply to the tumor- known as angiogenesis. The anti-metastasis properties of Sanguinarine and chelerythrine stops the spreading of cancer cells, while at the same time promotes cell cycle arrest by down regulating survivin. These two phytochemo agents have demonstrated multiple anti- drug resistance in clinical studies, while other studies have shown the potential for these components as a nutrient to prevent cancer cells from forming.
Studies have demonstrated that sanguinarine and chelerythrine induce apoptosis in cancer cells:
- Acute Myeloid Leukemia (Aml), 14, 21
- Breast Cancer (MCF-7) 28 highly metastatic breast cancer cell line MDA-MB-231 36, 41
- Bronchial carcinoid cell line human (NCI-H727, and NCI-H720)31
- Bone Cancer19
- B-cell lymphoma 2 (Bcl-2) 20
- B-cell lymphoma-extra-large (Bcl-xl) 20
- Cervical cancer 28
- Cardiac myocytes 28
- Colon carcinoma (HCT116) 28, 41
- Endocervical (Cervix) 28,
- Epidermoid carcinoma A431 cells human 13, 15, 22, 23, 28, and 29
- Erythroleukemia (K 562, JM1) 13, 28,
- Fibroblasts 28,
- Gastric 41
- histiocytic lymphoma (U 937) 28,
- Leukemia U937 cells human,
- Keratinocytes (HaCaT cells) 15, 22, 28
- Kidney 38
- Leukemia HL-60 cells and (K562 cells) human 14, 21
- Lung Non-Small Cell Carcinoma 28,
- Lymphoid 14,
- Myeloid leukemia cells14, 28
- Melanoma, A375 Human16 & Mouse Melanoma cell lines B16, 4A516, 28,
- Neuroblastoma (SH-SY5Y) 28,
- Uveal melanoma eye melanoma (OCM-1)28,35
- Non-Hodgkin's Lymphoma,
- Primary effusion lymphoma (PEL) 30,
- Premalignant cell line (HaCaT human Cells are utilized for their high capacity to differentiate and proliferate in the petri dish.)13.
- Pancreatic carcinoid cell line human (BON-1)31, 41
- Prostate carcinoma cells (Five different types cell types LNCaP, PC-3, DU-145, C4-2, and PZ-HPV7 human) 13, 22, 28, 37, 41,
- Osteosarcoma 32, 33,
- Ovary 39, 40, 41,
- Uterine cervical multidrug-resistant carcinoma cells (HeLa cells human) 13,
The interest in Sanguinarine and chelerythrine is increasing every year as new research demonstrates the effectiveness of the anticancer agents to kill all types of cancer cells. To date, all the research I have read has demonstrated that every cancer cell tested with Sanguinarine and chelerythrine has yielded positive results. Additionally, one of the little known actions about Sanguinarine is its ability to kill infections like MERSA. Research has demonstrated that sanguinarine killed resistant methicillin and resistant staphylococcus aureus in a dose dependent manner8.
Slippery Elm (Ulmus rubra) has a long history in the United States, first by the American Indians, and then listed in United States Pharmacopoeia from 1820 to 193624. The inner bark of this plant is what possesses the therapeutic properties. Slippery Elm has an emollient action which helps to hold and retain moisture in the G.I. track. It is known as a mucilaginous, demulcent agent as it soothes and heals the irritation of inflamed or injured skin and surfaces of the gastrointestinal track. It also contains plant based flavonols called oligomeric procyanidins. Slippery Elm exhibits antiseptic and anti-allergic actions, and promotes healthy kidney function4. Medical Slippery Elm is used to sooth irritated mucous membranes, treats ulcerations of the digestive tract,5 and is used to treat gastritis, gastric catarrh, mucous colitis and enteritis4.
The inner bark of Slippery Elm is also very nutritious. In fact, this highly nutritious food is made into gruel. The consistency is a thick mixture similar to porridge’s (whole grains are typically mixed with it). The gruel forms a nutritious wholesome food that is easily digested by infants and other who have impaired digestion4.
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.
TumorX Enzymes are able to
destroy the cancerous cells.
The photo below describes the outer shell of a cancerous cell.
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., amylase.
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 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 houlders 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 ineral 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.
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. Kelley 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.
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! Co-Enzyme Q10 is Dose Dependent. * 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.
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 prostate 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: 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. As of 2007, there were over 186,000 cases of cancer resulting from malnutrition, and the rates continue to grow!
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.
The fundamental difference between cancerous and non-cancerous cells is that cancerous cells do not respond to adjacent cell commands. 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.
Healthy Immune System Cures Cancer
A study reviewed the relation of Co-Enzyme Q10 to the regression of breast cancer. When 90 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 Q10.8,10 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.
Verification That You Are Cancer Free
The three best testing methods that I know of are the American Metabolic Laboratories, Ca Profile test, Dr. Navarro Cancer Test and the AMAS Test. The Navarro Test is a urine analysis to test for pregnancy. If the test indicates that you are pregnant you still have cancer. If the test indicates that you are not pregnant, you are cancer free.
The AMAS test checks for a protein that is found in cancer patients. This test can be ordered by a medical doctor and is available worldwide.
I believe you should steer clear of biopsy and other crazy ideas proposed by doctors. The problem with biopsy is that it creates needle scarring and pain. The problem with the before mentioned test is often false positives.
I would suggest that if you have a positive reading with either of these tests to have it performed a second time. If both tests return a positive then you in fact have cancer.