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Dr Raths discoveries and our research set up new therapeutic directions and present a
real chance to control cancer, all of which had not been possible with conventional
medicine approaches. We have demonstrated that a specific combination of natural
substances (vitamins, amino acids, polyphenols and other micronutrients) working in
biological synergy can successfully control critical aspects of malignancy in our body,
such as:
- Curtail metastasis (the spread of cancer to other organs)
- Inhibit tumor growth
- Decrease tumor angiogenesis (formation of new blood vessels feeding tumors)
- Trigger natural death of cancer cells through apoptosis.
Cancer is one of the most dreaded diseases affecting mankind. It is the second leading cause
of death in the industrialized countries and a significant health burden in other countries in the
world. Decades of scientific and clinical research conducted at leading institutions worldwide
have achieved marginal progress in managing this disease and a cure for it is not even in sight.
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chemical toxins, including certain medical drugs. About 50-75% of cancers have been
recognized as preventable since they are triggered by factors that can be avoided, such as
improper diets, micronutrient deficiencies or environmental pollutants.
Although there is a great diversity of these causative agents, the end cellular response is
always the same - the production of cells with the following characteristic which applies to most,
if not all, cancers.
1. Independent growth: Cancer cells multiply independently and at a different rate
compared to neighboring cells
2. Unlimited growth potential. Cancer cells lack biological signals which regulate and limit
their multiplication
3. Immortality of cancer cells. Due to an error in the genetic program which determines
the time of cell death (apoptosis) cancer cells do not die like all normal cells in the body which
have a limited life span
4. An ability to trigger growth of new blood vessels (Angiogenesis). Cancer cells send
biological signals that trigger formation of new blood vessels essential to support tumor growth
5. Invasion in the tissue and metastasis to other organs. Cancer expansion is possible
because malignancy triggers uncontrolled digestion of collagen and connective tissue paving
the way for cancer cells to invade and spread.
Conventional therapies
The majority of current therapies are not cancer-specific and do not curtail the spread of cancer
to different organs. They are based on the use of highly toxic chemical agents (chemotherapy)
and radiation (radiotherapy). Both treatments generate serious side effects, organ damage and
secondary cancers. As a result, these treatments have not been successful in controlling cancer
and on the contrary, many cancers are increasing.
Comprehensive review of the effectiveness of chemotherapy in 22 types of cancer has shown
that these highly toxic treatments increase a chance for five-year survival by merely 2.1% and in
many types of cancer, chemotherapy does not offer any benefits (Clinical Oncology 2004).
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The basis of chemotherapy and radiation is the destruction of rapidly dividing cells, such as
cancer cells. However, these treatments do not discriminate between healthy and abnormal
(cancer) cells. As a result they also damage cells in healthy organs that have a high renewal
rate and are frequently dividing, such as the cells of bone marrow, skin, the intestinal lining and
many other organs. Therefore a frequent consequence of these therapies is anemia and
weakening of the immune system further impairing the elimination of cancer cells. Intestinal
bleeding triggered by these therapies impairs the absorption of nutrients and contributes to
diminishing the bodys natural ability to fight cancer. The consequence of the administration of
such powerful chemical toxins or radiation is damage to the genetic machinery of the cells, the
DNA, leading to development of new cancers. These interventions also activate the secretion of
enzymes that facilitate the release of cancer cells from the surrounding connective tissue
accelerating the spread of cancer to other organs. Chemotherapy often fails since many cancer
cells develop resistance to these toxic agents.
In this situation approximately 80% of patients diagnosed with cancer seek alternative
therapies, which include antioxidants and other essential nutrients.
In 1990 Dr. Rath presented a new research approach that can lead to effective control of the
growth and spread of cancer. This research focus is on strengthening the integrity of a natural
barrier made of collagen and other connective tissue elements which surround all cells,
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including cancer cells. In order to grow and spread to other organs every type of cancer cells
have to disintegrate (digest) this natural collagen and connective tissue barrier with the help of
specific enzymes. To halt this collagen digestion process, Dr Rath proposed the use of natural
components, vitamin C and the amino acid lysine.
The main reason cancer is so difficult to control is that it adapts to the bodys natural
mechanisms to expand in the tissue and relocate to other organs.
Most cells in the body are capable of producing enzymes that dissolve the surrounding collagen
and connective tissue (collagenases, proteinases). In a healthy body this ability is essential for
maintaining normal body function, tissue repair and restructuring. For instance, enzymatic
degradation of connective tissue forms an integral part of immune system effectiveness (i.e.,
allows for migration of white blood cells to infection sites), the function of reproductive organs
(release of an egg in the female monthly cycle, remodeling of breast and uterine tissue
occurring in pregnancy and lactation) and during growth. This collagen dissolving mechanism is
well controlled in a health body.
However, the same mechanism shifts out of control in a disease condition, such as cancer. In
this case a persistent secretion of collagen destroying enzymes by cancer cells leads to tissue
degradation facilitating tumor growth and metastasis. In addition, uncontrolled collagen
dissolving accompanies other pathologies, such as chronic inflammation (arthritis, asthma,
atherosclerosis), infections (destruction of connective tissue facilitates spread of microbial
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agents) and in many other conditions. (For more information, please click here .)
In the case of cancer, the importance of controlling connective tissue destruction mechanism
has been confirmed by Danish researchers using a transgenic mouse model. Their study has
shown that genetically modified mice which are unable to produce the enzyme urokinase which
is needed to degrade collagen, have a limited ability to form cancer metastasis. ( K. Almholt et
al., Reduced metastasis of transgenic mammary cancer in urokinase deficient mice, Int J
Cancer 2005; 113(4): 525-532
)
There are many enzymes involved in digesting connective tissue proteins, such as plasmin,
urokinase and various types of matrix metalloproteinases (MMPs). The main enzymes
associated with malignancy are MMP 2 and MMP 9. Their activity has been linked to the
aggressiveness of cancer. Interestingly, tissues which have natural remodeling potential and
therefore can produce large quantities of these collagen digesting enzymes (i.e., tissues in the
breasts, ovaries, and bone marrow) have a high susceptibility to develop cancer. Dr Rath has
provided an explanation to this phenomenon
.
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cancer cells in the tissue and control other key mechanisms of cancer at the same time. This
synergy utilizes vitamin C, the amino acids lysine, proline, arginine, N acetylcysteine, green tea
extract (NM) as well as copper, manganese and selenium.
Using both in vitro and in vivo approaches, we provided comprehensive scientific data that this
nutrient synergy can:
1. Inhibit tumor growth and cancer metastasis:
The following relevant mechanisms have been affected by this nutrient synergy
- Inhibition of secretion and expression of MMPs curtailing connective tissue digestion
- Inhibition of cancer cells invasion in the tissue (confirmed in almost 40 types of cancer
cells)
- Optimizing composition of connective tissue towards increasing its integrity and
resistance to degradation
- Decreased cell multiplication resulting in the inhibition of tumor growth.
As a result we demonstrated in vivo that the spread (metastasis) of cancer cells can be largely
inhibited by the administration of nutrient synergy in the diet or by iv and ip delivery.
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4. Decrease inflammation
The following relevant mechanisms have been affected by this nutrient synergy
- Impaired secretion of various pro-inflammatory factors, which have been implicated in the
induction and progression of cancer
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