Angiogenesis is the creation of new blood vessels, a process that occurs in both health and disease. When new tissue is formed, as in the healing of a wound or the creation of the placenta, blood vessel formation must occur as well. The body is awash in factors that act to signal the growth and differentiation of various cells, including those of the arteries and veins, and the arterioles, venules, and capillaries. The control of angiogenesis operates through a series of “on” and “off” switches that either stimulate or inhibit the formation of new vessels. If there are too many “ons” and insufficient “offs,” the upset of balance favors the growth of new blood vessels. The opposite also holds true. If a person is healthy, the balance is easily maintained, but in some disease states things get out of hand, in either direction—too many or too few new vessels. You see, tumors also need a blood supply. The nutrients and growth factors supplied by the new blood vessels allow tumors to grow. Because of this, the search for ways to destroy cancer cells is partly focused on anti-angiogenesis. But having too many blood vessels is not limited to tumors. Diseases of the eye (macular degeneration, for example) and chronic inflammatory diseases, such as rheumatoid arthritis, psoriasis, and periodontal disease are also characterized by proliferation of vascular tissue. (Polverini. 1995) And researchers at the University of British Columbia believe that Alzheimer’s disease may be related to hypervascularization. (Biron. 2011)
Substances that prevent the formation of new blood vessels have been around for awhile. Thalidomide is one of them. This drug caused quite a stir in the 1950’s and 60‘s, after it was found to cause skeletal birth defects. Prescribed as a sedative to prevent morning sickness, thalidomide caused thousands of congenital disorders before it was reined in. Because it has benefits for leprosy patients and some inflammatory and autoimmune disorders, it’s still available. Additionally, its antiangiogenic character makes it an appropriate choice for the treatment of multiple myeloma, a primary tumor of bone marrow. (Singhal. 1999) (Bamias. 2003) If thalidomide is able to interrupt the formation of new blood vessels, you can easily see how the development of a neonate can be disrupted.
To study the effects of antiangiogenic substances, some scientists have chosen fat as the experimental system because of its remodeling capacity. Here they have learned that the manufacture of new blood vessels is important to the viability of adipose tissue, and that if the neovascularization were halted, so would be the proliferation of fat cells. (Rupnick. 2002) This transfer of concept to tumor cells is encouraging. A signaling protein termed VEGF (vascular endothelial growth factor) stimulates the growth of new blood vessels, and it helps to restore the oxygen supply to tissues when blood circulation is inadequate. Its importance in embryonic development is obvious, but its overexpression can be problematic. Solid tumors need VEGF to grow beyond their normally limited size, so they make their own. On the other hand, the body makes angiogenic inhibitors, such as thrombospondin and angiostatin to keep tumors dormant. ( Huang. 2004) Besides thalidomide, there are numerous pharmaceuticals available to interrupt angiogenesis, including bevacizumab (Avastin®) and other monoclonal antibodies, the side effects of which offer a laundry list of ills, including cancer. (Hansel. 2010) How ironic! The majority of these drugs block the activity of VEGF, but there may be other angiogenic factors about which less is known.
Working on the antiangiogenesis strategy proposed by renowned cancer researcher, Judah Folkman, Dr. William Li, of the Angiogenesis Foundation in New York, looked beyond drugs and their costs and toxicity, and identified powerful antiangiogenic molecules in dietary sources. This suggests that dietary enlightenment could offer a safe, readily available, novel strategy for preventing cancer. (Folkman. 2006) (Li. 2012)
Dr. Li discovered that nature has loaded a number of foods, beverages and herbs with naturally occurring inhibitors of angiogenesis: berries, citrus fruits, cruciferous vegetables, mushrooms, tomatoes, red wine, green tea, parsley, garlic, turmeric and dark chocolate, among others. The laboratory names extracted from these foods include brassanin, curcumin, genistein, N-acetylcysteine, resveratrol, silymarin, and selenium. The last-named is the only antioxidant mineral. ( Li. 2012)
A study in India, at the Himalayan Institute of Medical Sciences, found aberrant angiogenesis to be factored in Alzheimer’s disease and AIDS, comparing the modulation of angiogenesis in this century to the antibiotics of the twentieth century. (Bisht. 2010) Sagar, Yance and Wong, working at the McMaster University Department of Medicine, in Ontario, added a litany of herbs to Dr. Li’s initial list, citing their antiangiogenic behavior as being engaged through several interdependent processes that include effects on gene expression and enzyme activities. Besides inhibiting the formation of new vascular tissue, these may directly hinder tumor progression and reduce metastasis by way of other actions, including the interruption of epidermal growth factor reception, the blocking of the cyclooxygenase-2 enzyme, and the obstruction of nuclear factor kappa-B transcription. The herbals, artemisia annua (Chinese wormwood), viscum album (European mistletoe), curcuma longa (curcumin), resveratrol, quercitin, ginger, Panax ginseng, and proanthocyanidin (grape seed extract) are among them. (Sagar, Yance and Wang. 2006)
Not only has a soy-based diet, but also the isolated soy isoflavone, genistein, exhibited anti-cancer properties, particularly in lines of melanoma and mammary carcinoma. As is the case with most non-drug treatments, effect is dose-dependent. Its behavior suggests interference with tumor cell migration. (Farina. 2006) The medicinal mushroom, Agaricus blazei Murrill, common to the tropical rain forests near Sao Paulo, Brazil, has traditionally been used to stimulate the immune system, to treat digestive and circulatory disorders, and to lower cholesterol. But its lipid fraction, ergosterol, which is converted to vitamin D2 when exposed to UV radiation, was found to reduce tumor growth significantly in sarcoma-bearing mice at doses of 400+ mg/kg without side effects, suggesting that either ergosterol or its metabolites inhibits tumor-induced neovascularization. (Takaku. 2001) This is the first report of ergosterol’s antiangiogenic character. Later study of this mushroom found additional antiangiogenic constituents. (Kimura. 2004)
Another popular medicinal mushroom is Ganoderma lucidum, used largely in East Asia. Its attributes include the induction of programmed cell death in tumors (apoptosis), accompanied by the inhibition of cell proliferation and suppression of cell migration, especially in prostate cancer, where VEGF was down-regulated. (Stanley. 2005) It is desirable to keep cancer growth stagnant for as long a time as possible. Black raspberry extract was able to do that, as identified in research at Louisiana State University, where investigators saw potent inhibition of angiogenesis and concomitant vessel growth. Gallic acid was pinpointed as a major agent, which worked best in conjugation with less potent fractions, the synergy of which has yet to be elucidated. (Zhijun. 2005)
By disrupting the growth of new vessels from pre-existing capillaries, the green tea catechin, epigallocatechin gallate (EGCG) interrupts cell tube formation in the angiogenesis process by stopping VEGF signals from reaching their receptors. (Rodriguez. 2006) Likewise, blueberries are antiangiogenic. But these little beauties also have the distinction of being able to regenerate rhodopsin, the ocular molecule responsible for turning light energy onto nerve signals. Chinese researchers also found that blueberries can help to forestall a few age-related chronic diseases, such as diabetes, hyperlipidemia, hypertension, neurodegeneration, and even obesity through its apoptosis, antioxidant and anti-inflammation effects. (Chen. 2010)
If there is a favorite among anti-cancer alternative treatments, curcumin might hog the spotlight. Chemoprevention—the use of chemicals to prevent the development of cancer—is a promising anti-cancer approach with limited side effects compared to traditional chemotherapy. Curcumin, isolated from the kitchen spice turmeric, demonstrates the capability of suppressing, retarding, and even inverting carcinogenesis. It is able to induce apoptosis in cancer cells without cytotoxic effects on healthy cells while inhibiting the formation of tumors. It is well tolerated and is selective for cancer cells. (Lopez-Lazaro. 2008) No definitive dose has been identified, but trials using up to 8,000 mg a day have found no adverse effects. Its particular effectiveness appears to lie in colon cancer lines (Johnson. 2007), but its antiproliferative effects may extend to others (Hanif. 1997) (Lopez-Lazaro. 2008) The military can win a war by cutting off the enemy’s supplies. Could the war on cancer do the same?
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