Integrity


RESEARCH
  • Low cancer death rates in green tea consuming countries and countries with diets high in chili peppers.
  • Green tea appears to block growth of new blood vessels that tumors require for growth and metastasis.
  • Green tea catechin EGCg inhibits special enzyme cancer cells secrete to penetrate and colonize tissue.
  • Green tea enhances the effectiveness of conventional therapies.
  • EGCg inhibits telomerase, the enzyme that "immortalizes" cancer cells.
  • Capsaicin inhibits tNOX.
  • In 1999 Congress appropriated funds for NIH to establish botanical research initiative.
  • In 2000 Purdue University awarded grant by NIH to participate in botanical research initiative.

     The final decade of the twentieth century brought exciting new research into the role played by green tea in the pursuit of good health and longevity. Epidemiologists have long noted that people in green tea consuming countries (primarily China and Japan) have low death rates from cancer. In addition, they have noted that countries (especially Thailand and Mexico) that consume diets high in capsaicin, the pungent (hot) principle of chili peppers, also have significantly low death rates from cancer.

     The potential health benefits of green tea are being studied extensively. This ongoing research, which has been published in prestigious academic journals, indicates that the catechins of green tea (also known as polyphenols) exhibit potential anti-cancer and cancer-fighting health benefits. The catechin epigallocatechin gallate (EGCg) is thought to be the one of the most important constituents of green tea. Capsaicin, though less studied than green tea, has also been shown to have potential anti-cancer and cancer-fighting health benefits.

     Research suggests that drinking tea, green tea in particular, lowers the incidence of breast, prostate and lung cancer. In fact, there is mounting evidence that green tea may be effective against more types of cancer including colon, stomach, pancreatic, skin cancer, leukemia, and glioma. Researchers in Stockholm, Sweden at the Karolinska Institute discovered that green tea appears to block angiogenesis or the development of new blood vessels that cancerous tumors require for growth and metastasis. If more studies confirm these findings, it may help to explaining why green tea is effective against so many kinds of cancer.

     Cancer cells secrete special enzymes called collagenases that enable the cells to penetrate and colonize tissue-the metastatic process. A study done in Japan at the University of Shizuoka reported that EGCg inhibits the secretion of the enzyme collagenases. In another study at the same university conducted with ovarian cancer patients, researchers found that theanine, an amino acid found in the leaves of green tea, synergized with the chemotherapy Adriamycin in lowering tumor weight. Adriamycin alone was ineffective. Their recent research has also shown that theanine also synergized with Adriamycin to inhibit liver metastases of ovarian cancer. Studies using human cancer cell culture found that the effect of tea catechins was synergistically increased when catechins were combined with other anti-cancer agents such as tamoxifen, capsaicin, and curcumin as well as Adriamycin. This adds to the growing evidence that natural agents such as green tea can greatly enhance the effectiveness of conventional therapies.

     A recent 7 year study in Japan found that women with stage I or II breast cancer who consumed five or more cups of green tea daily had about half the recurrence rate of those who drank four or less cups a day. In Tokyo a study at the Cancer Chemotherapy Center using leukemia and colon cancer cell cultures showed that EGCg inhibited telomerase, the enzyme that "immortalizes" cancer cells. Inhibition of telomerase is considered an important anticarcinogenic mechanism.

     A recent study at Purdue University identified and investigated an enzyme associated with all forms of cancer. The newly identified enzyme,
tNOX (the tumor-associated form of NOX), is expressed by cancer cells all the time and is common to all forms of cancer. The normal enzyme NOX, or quinol oxidase, is required for growth and is expressed only when cells are dividing. The researchers determined that when cells were exposed to EGCg the cancer cells failed to grow and reach the minimum size needed for division. The cancer cells then underwent programmed cell death or apoptosis. EGCg had no effect on the NOX of normal cells.

    
Capsaicin, the pungent (hot) principle of chili peppers, has also been shown to inhibit tNOX. Before the proprietary process of modifying capsaicin for exclusive use in Capsibiol-T® was developed, the dosage required for capsaicin to be effective (its therapeutic dosage) had exceeded the level at which its pungency and neurological discomfort (heat) could be tolerated.

     In 1999 Congress appropriated funds for the Office of Dietary Supplements (ODS) at the
National Institutes of Health (NIH) in collaboration with the National Center for Complementary and Alternative Medicine (NCCAM) to develop and establish a botanical research center initiative with major research institutions. Its purpose is to foster research to identify potential health benefits and a systematic evaluation of the safety and effectiveness of botanicals available as dietary supplements. To date four institutions have been awarded grants-in 1999, UCLA and the University of Illinois-Chicago and in 2000, Purdue University and the University of Arizona.

REFERENCES
Published research regarding cancer fighting and cancer preventive benefits of green tea and capsaicin.



Please View Website Disclosure Message


About Capsibiol-T
Frequent Questions
Glossary of Terms
Research
Ordering Procedure
Website Security
Privacy Policy
Contact Information

Order Status

View Cart/Checkout

PLACE ORDER

Printable Version