Technical Data
DESCRIPTION
Protective Breast Formula is a combination of clinically and scientifically studied ingredients that support the immune system and cellular health.
It includes turmeric extract, Indoplex® with DIM, calcium d-glucarate, maitake d-fraction, green tea extract, grape seed extract and vitamin D3, bringing together some of the most widely-studied ingredients that support immune health.
This formula was developed in association with Christine Horner, MD, FACS, an expert in the field of women's breast health.
Protective Breast Formula:
- Combines the best-researched ingredients that support breast tissue health
- Specifically formulated to provide optimum benefits for women
- Includes the potent natural immune boosters and antioxidants: Indoplex®, green tea extract, maitake D-fraction, turmeric, vitamin D3 cholecalciferol and grape seed extractm/LI>
- Recommended by women's health expert, Dr. Christine Horner
- Supports breast tissue health through five separate, unique pathways
HOW DOES IT WORK?
FIVE PATHWAYS TO BREAST HEALTH:
Optimal breast health depends on a complex interplay of factors. A woman's diet, her environment, and even the level in stress in her life play a role in her health experience. The ingredients in Protective Breast Formula™ were selected because each provides demonstrated breast health support through one or more different pathways, including antioxidants, hormone detoxification, and immune system support.
When used in conjunction with a balanced diet and healthy lifestyle choices, Protective Breast Formula provides superior support for breast tissue health.
1. Antioxidant
Human cells are constantly being exposed to unstable molecules known as free radicals. These compounds steal electrons from other molecules to stabilize themselves, thereby creating a new unstable free radical and starting a chain reaction of free radical formation. Exposure to free radicals is not associated with optimal health.
Free radicals form as a normal part of body function, or in response to exposure to toxins such as cigarette smoke, air pollution, or even ultraviolet rays from the sun. The human body has a built in system to neutralize free radicals with the help of antioxidants. These compounds donate an extra electron to a free radical (making it stable) but do not then become free radicals themselves. If the amount of free radical formation is greater than the amount of available antioxidants, this may lead to oxidative stress and potential harm to cells. Supplemental antioxidants from food or supplements can boost the body's own natural antioxidant defenses.
Grape seed extract is a powerful antioxidant ingredient found in Protective Breast Formula. In a scientific study, grape seed extract even exhibited more powerful antioxidant activity than vitamins C and E.1
Other research has shown that the antioxidant activity of grape seed extract aids in the overall functioning of healthy cellular production and immune support. A recent study in an animal model found that grape seed extract was associated with a 50% increased benefit in breast cell health.2,3
Green tea is well known for its antioxidant abilities as well. Green tea compounds, called polyphenols or catechins are the components studied for their beneficial effects. To date, most research has centered around a catechin of green tea called epigallocatechin-3-gallate, or simply, EGCG. In scientific and clinical studies, EGCG from green tea works as an overall antioxidant and a powerful scavenger of free radicals. Specifically, studies have found EGCG supports healthy breast cell development.4,5
Green tea has been shown in research studies to both increase the activity of antioxidant production systems (glutathione peroxidase and superoxide dismutase enzyme), as well as protect lipids and proteins from oxidation. Finally green tea has also shown COX-2 inhibition, and support for healthy cell replication and development.6,7
2. Natural Inflammatory Response
Inflammation is a natural process, and may occur throughout the body. The inflammatory response can be triggered by many factors, including poor diet, physical injury, and invading microorganisms. A healthy inflammatory response involves activation of inflammatory compounds including prostaglandins, leukotrienes, and cytokines. Research has now found that inflammation also plays a role in cell development.8
COX-2 and inflammation
The cyclooxygenase enzyme plays an important role in the production and regulation of prostaglandins, the hormone-like compounds that regulate many biochemical processes in the body. The enzyme exists in two primary forms, cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2). An imbalance of the COX-2 enzyme may lead to the development of inflammation and generation of free radicals. Additionally, a high level of COX-2 enzyme active is not associated with healthy cell development.8-14
Because of its important role in the inflammatory cascade, much research has focused on COX-2 inhibition. COX-2 inhibitors decrease prostaglandin production, thereby halting the inflammatory cascade.
Recent research also shows a link between COX-2 inhibition and support of healthy breast tissue formation. 8-14
In scientific studies, turmeric shows COX-2 inhibition and general support for healthy cell development. Turmeric seems to be COX-2 preferential—not inhibiting the activity of the beneficial COX-1 enzyme involved in supporting the stomach lining. Additional recent research has investigated turmeric's ability to scavenge free radicals.15-19
3. Hormone Balance:
Estrogen is an important hormone for women, as it stimulates the development and function of female characteristics and sexual reproduction. Estrogen also plays a role in supporting healthy cell development, especially in the tissues of the breast and ovaries.
Interestingly, there are compounds in the environment called “xenoestrogens” that can mimic the effect of estrogen in the body, landing on estrogen receptor sites and stimulating cell activity. However, many of these xenoestrogens come from environmental pollutants and pesticides, and their estrogenic activity has a much more potent effect than natural estrogen made by the body. Xenoestrogens can also block the cell receptor site, preventing natural estrogen from doing its job, and may contribute to estrogen dominance.
Promoting healthy hormone balance involves limiting exposure to environmental xenoestrogens, and supporting the body's own hormone balancing mechanisms. For years, an observational association has been noted between healthy estrogen balance and a high dietary intake of vegetables, such as broccoli, cauliflower, and cabbage. Scientific study determined that such cruciferous vegetables contain several phytochemicals, including diindolylmethane (DIM).20-24
DIM acts as a natural hormone detoxifier, helping the body to efficiently and effectively break down and excrete estrogen. Metabolism occurring via the C-2 pathway in the liver increases the chances for estrogen to be broken down into 2-hydroxyestrone (2-OH1) and 2-hydroxyestradiol (2-OH2), estrogen metabolites known for their health supporting activities and promotion of healthy cell development.25-32
DIM shifts estrogen metabolism to the beneficial C-2 pathway in the liver. Research has shown that consumption of DIM increases the ratio of desirable 2-hydroxy and 2-methoxy estrogen metabolites over the undesirable 16-hydroxyestrone estrogen metabolites. 25 Scientific studies have also found that DIM directly supports healthy cell development in breast tissue.33-39
4. Immune Health:
The immune system includes cells and organs whose purpose is to defend the body from external invaders and internal malfunctions. Immune system cells, including macrophages, B and T cells, and natural killer cells detect and destroy foreign and potential harmful molecules – including bacteria, viruses, and damaged cells. Breast tissue health is tightly linked to healthy immune system function. Two ingredients in Protective Breast Formula™, maitake mushroom extract and cholecalciferol (vitamin D3) were specifically included in the formula to provide immune system support.
Maitake and Maitake-D-Fraction: Maitake (Grifola frondosa) mushrooms grow in clusters and have a leafy appearance (hence the “frondosa” or “fronds” of its Latin name). When eaten as food, they are noted for their woodsy taste, and are used as side dishes and additions to main ingredients. Extracts of maitake have also been investigated for their effects on immune system health and cellular development.
D-fraction is one of the key compounds in maitake mushrooms. Its primary benefit is to boost the activity of important immune system cells. In a clinical study, maitake D-fraction enhanced natural killer cell activity by 1.2 to 2.7 times.40
Other clinical and scientific studies have been encouraging as well, showing that maitake D-fraction induced a healthy immune system and cellular response. All the participants in a clinical study experienced increased natural killer activity and support of healthy cellular development.41
The benefits of vitamin D for bone health have been well documented. New epidemiologic studies have now shown that higher dietary intake of vitamin D is associated with support for breast health. Cholecalciferol, the biologically active form of vitamin D (also known as vitamin D3) is now the focus of research to determine exactly how vitamin D's benefits for breast tissue are attained.42,43
Scientific studies have shown that cholecalciferol encourages healthy cell growth and cell differentiation. These studies show that cholecalciferol enhances the body's own natural immune defense, support normal cellular health and support TNF-alpha (a protein involved with inflammation)-induced defense of breast cell tissues.44,45
5. Detoxification:
The process of detoxification refers to the breakdown and excretion of substances that are no longer needed or may be harmful to the body. One of the ways in which the body excretes hormones and toxins is by binding them to glucuronic acid in the liver, and then excreting this compound in the bile. However, this process can be disrupted by â-glucuronidase, an enzyme that produced by intestinal bacteria. This enzyme has the ability to break (uncouple) the chemical bond established by glucuronic acid. This action releases the bound toxins, which are then reabsorbed into the body instead of being excreted.
Calcium D-Glucarate is the calcium salt of d-glucaric acid. Naturally occurring both in the human body, and in certain plant sources, supplementation with calcium d-glucarate has been shown in research studies to support immune system function, promote estrogen metabolism, and enhance the body's detoxification systems through inhibition of beta-glucuronidase. By decreasing the portion of active compounds that could be hazardous to the body through its inhibition of D-glucuronidase, calcium d-glucarate provides significant support of breast tissue health.46,47
Five Pathways for Support of Breast Health
| Pathway |
Ingredient |
| Antioxidants |
Grape seed extract quenches free radicals and has more powerful antioxidant activity than vitamins C and E.1
Green tea extract contains the compound EGCG, a powerful scavenger of free radicals that supports healthy cell proliferation.5 |
| Natural inflammatory response |
Turmeric shows COX-2 inhibition and general support for healthy cell development. Turmeric appears to be COX-2 preferential—not inhibiting the activity of the beneficial COX-1 enzyme involved in supporting the stomach lining.18 |
| Healthy hormone balance |
DIM acts as a natural hormone detoxifier, helping the body to efficiently and effectively break down and excrete estrogen into beneficial, rather than undesirable, metabolites.36 |
| Immune system support |
In a clinical study, maitake D-fraction enhanced natural killer cell activity by 1.2 to 2.7 times.40
In recent studies, vitamin D3 (cholecalciferol) enhanced the body's own natural immune defense, supported normal cellular health and supported TNF-alpha (a protein involved with inflammation)-induced defense of breast cell tissues.44 |
| Detoxification |
Calcium d-glucarate helps bind spent hormones (estrogen) and other compound to transport them out of the body.46 |
RECOMMENDATIONS
Two tablets daily with food. If desired, take one tablet twice daily with food. For more active support, take two tablets twice daily.
PRECAUTIONS
Do not use if pregnant or nursing. Harmless changes in urine color may occur with the use of this product. If taking prescription drugs, consult your healthcare practitioner prior to use.
HOW IS IT SUPPLIED?
STORAGE RECOMMENDATIONS
Store at controlled room temperature, 59° to 86°F (15°-30°C)
REFERENCES
- Bagchi D, Garg A, Krohn RL, Bagchi M, Tran MX, Stohs SJ. Oxygen free radical scavenging abilities of vitamins C and E, and a grape seed proanthocyanidin extract in vitro. Res Commun Mol Pathol Pharmacol. 1997;95(2):179-89.
- Kim H, Hall P, Smith M, Kirk M, Prasain JK, Barnes S, Grubbs C. Chemoprevention by grape seed extract and genistein in carcinogen-induced mammary cancer in rats is diet dependent. J Nutr. 2004 Dec;134(12 Suppl):3445S-3452S.
- Zhao J, Wang J, Chen Y, Agarwal R. Anti-tumor-promoting activity of a polyphenolic fraction isolated from grape seeds in the mouse skin two-stage initiation-promotion protocol and identification of procyanidin B5-3'-gallate as the most effective antioxidant constituent. Carcinogenesis. 1999;20(9):1737-1745.
- Morley N, Clifford T, Salter L, Campbell S, Gould D, Curnow A. The green tea polyphenol (-)-epigallocatechin gallate and green tea can protect human cellular DNA from ultraviolet and visible radiation-induced damage. Photodermatol Photoimmunol Photomed. 2005;21(1):15-22.
- Roy AM, Baliga MS, Katiyar SK. Epigallocatechin-3-gallate induces apoptosis in estrogen receptor-negative human breast carcinoma cells via modulation in protein expression of p53 and Bax and caspase-3 activation. Mol Cancer Ther. 2005 Jan;4(1):81-90.
- Noreen Y, Serrano G, Perera P, et al. Flavan-3-ols isolated from some medicinal plants inhibiting COX-1 and COX-2 catalysed by prostaglandin biosynthesis. Planta Med. 1998 Aug;64(6):520-4
- Luczaj W, Waszkiewicz E, Skrzydlewska E, Roszkowska-Jakimiec W. Green tea protection against age-dependent ethanol-induced oxidative stress. J Toxicol Environ Health A. 2004;67(7):595-606.
- Michael MS, Badr MZ, Badawi AF. Inhibition of cyclooxygenase-2 and activation of peroxisome proliferator-activated receptor-gamma synergistically induces apoptosis and inhibits growth of human breast cancer cells. Int J Mol Med. 2003;11(6):733-6.
- Costa C, Soares R, Reis-Filho JS, et al. Cyclo-oxygenase 2 expression is associated with angiogenesis and lymph node metastasis in human breast cancer. J Clin Pathlo. 2002;55(6):429-34
- Howe LR, Dannenberg AJ, A role for cyclooxygense-2 inhibitors in the prevention and treatments of cancer. Semin Oncol. 2002;29 (Suppl 11):111-9
- Kundu N, Smyth MJ, Samsel L, et al. Cyclooxygenase inhibitors block cell growth, increase ceramind and inhibit cell cycle. Breast Cancer Res Treat. 2002;76(1):57-64
- Lu S, Zhang X, Badawi AF, et al. Cyclooxygenase-2 inhibitor celecoxib inhibits promotion of mammary tumorigenesis in rats fed a high fat diet rich in n-polyunsaturated fatty acids. Cancer Lett. 2002;184(1):7-12
- Singh B, Lucci A, et al. Role of Cyclooxygenase-2 in breast cancer. J Surg Res 2002 Nov,108(1):173-9.
- Spizzo G, Gasti G, Wolf D, et al. Correlation of COX-2 and Ep-CAM overexpression in human invasive breast cancer and its impact on survival. Br J Cancer. 2003 Feb 24;88(4):574-8
- Tilak JC, Banerjee M, Mohan H, Devasagayam TP. Antioxidant availability of turmeric in relation to its medicinal and culinary uses. Phytother Res. 2004;18(10):798-804. PMID: 15551376
- Rukkumani R, Aruna K, Varma PS, Rajasekaran KN, Menon VP. Comparative effects of curcumin and an analog of curcumin on alcohol and PUFA induced oxidative stress. J Pharm Pharm Sci. 2004;7(2):274-83. PMID: 15367386.
- Balasubramanyam M, Koteswari AA, Kumar RS, Monickaraj SF, Maheswari JU, Mohan V. Curcumin-induced inhibition of cellular reactive oxygen species generation: novel therapeutic implications. J Biosci. 2003 Dec;28(6):715-21. PMID: 14660871
- Zhang F, Altorki NK, Mestre JR, Curcumin inhibits cyclooxygenase-2 transcription in bile-acid and phorbol ester-treated human gastrointestinal epithelial cells. Carcinogenesis. 1999 Mar;20(3):45-51
- Shah BH, Nawaz Z, Pertani SA, et al. Inhibitory effect of curcumin, a food spice from turmeric, on platelet-activating factor-and arachidonic acid mediated platelet aggregation through inhibition of thromboxane formulation and Ca2+ signaling. Biochem Pharmacol. 1999;58:1167-1172.
- Verhoeven DT, Goldbohm RA, van Poppel G, Verhagen H, van den Brandt PA. Epidemiological studies on brassica vegetables and cancer risk. Cancer Epidemiol Biomarkers Prev. 1996;5:733-748.
- Kolonel LN, Hankin JH, Whittemore AS, et al. Vegetables, fruits, legumes and prostate cancer: a multiethnic case-control study. Cancer Epidemiol Biomarkers Prev. 2000;9:795-804.
- Fahey JW, Zhang Y, Talalay P. Broccoli sprouts: an exceptionally rich source of inducers of enzymes that protect against chemical carcinogens. Proc Natl Acad Sci U S A. 1997;94:10367-72.
- Brooks JD, Paton VG, Vidanes G. Potent induction of phase 2 enzymes in human prostate cells by sulforaphane. Cancer Epidemiol Biomarkers Prev. 2001;10:949-954.
- Jellinck PH, Forkert PG, Riddick DS, Okey AB, Michnovicz JJ, Bradlow HL. Ah receptor binding properties of indole carbinols and induction of hepatic estradiol hydroxylation. Biochem Pharmacol. 1993;45:1129-36.
- Zeligs MA. Safer estrogen with phytonutrition. Towns Lett. 1999;189:83-88.
- Bradlow HL, Telang NT, Sepkovic DW, Osborne MP. 2-hydroxyestrone: the 'good' estrogen. J Endocrinol. 1996;150:259-65.
- Meilahn EN, De Stavola B, Allen DS, et al. Do urinary oestrogen metabolites predict breast cancer? Guernsey III cohort follow-up. Br J Cancer. 1998;78:1250-5.
- Maran A, Zhang M, Kennedy AM, et al. 2-methoxyestradiol induces interferon gene expression and apoptosis in osteosarcoma cells. Bone. 2002;30:393-8.
- Singh A, Purohit A, Hejaz HA, Potter BV, Reed MJ. Inhibition of deoxyglucose uptake in MCF-7 breast cancer cells by 2-methoxyestrone and 2-methoxyestrone-3-O-sulfamate. Mol Cell Endocrinol. 2000;160:61-6.
- Djavaheri-Mergny M, Wietzerbin J, Besancon F. 2-Methoxyestradiol induces apoptosis in Ewing sarcoma cells through mitochondrial hydrogen peroxide production. Oncogene. 2003;22:2558-67.
- Raobaikady B, Purohit A, Chander SK, Woo LW, Leese MP, Potter BV, Reed MJ. Inhibition of MCF-7 breast cancer cell proliferation and in vivo steroid sulphatase activity by 2-methoxyoestradiol-bis-sulphamate. J Steroid Biochem Mol Biol. 2003;84:351-8.
- Tinley TL, Leal RM, Randall-Hlubek DA, Cessac JW, Wilkens LR, Rao PN, Mooberry SL. Novel 2-methoxyestradiol analogues with antitumor activity. Cancer Res. 2003;63:1538-49.
- Lippert C, Seeger H, Mueck AO, Lippert TH. The effects of A-ring and D-ring metabolites of estradiol on the proliferation of vascular endothelial cells. Life Sci. 2000;67:1653-8.
- Fowke JH, Longcope C, Hebert JR. Brassica vegetable consumption shifts estrogen metabolism in healthy postmenopausal women. Cancer Epidemiol Biomarkers Prev. 2000;9(8):773-9.
- Michnovicz JJ, Bradlow HL. Dietary and pharmacological control of estradiol metabolism in humans. Ann NY Acad Sci. 1990;595:291-299.
- Michnovicz HH, Bradlow HL. Altered estrogen metabolism and excretion in humans following consumption of indole-3-carbinol. Nutr Cancer. 1991;16:59-66.
- Firestone GL, Bjeldanes LF. Indole-3-carbinol and 3-3'-diindolylmethane antiproliferative signaling pathways control cell-cycle gene transcription in human breast cancer cells by regulating promoter-Sp1 transcription factor interactions. Nutr. 2003;133(7 Suppl):2448S-2455S.
- Ge X, Yannai S, Rennert G, Gruener N, Fares FA. 3,3'-diindolylmethane induces apoptosis in human cancer cells. Biochem Biophys Res Commun. 1996;228(1):153-8.
- Hong C, Kim HA, Firestone GL, Bjeldanes LF. 3,3'-diindolylmethane (DIM) induces a G(1) cell cycle arrest n human breast cancer cells that is accompanied by Sp1-mediated activation of p21 (WAF1/CIP1) expression. Carcinogenesis. 2002;23(8):1297-305.
- Kodama N, Komuta K, Sakai N, Nanba H. Effects of D-fraction, a polysaccharide from Grifola frondosa on tumor growth involve activation of NK cells. Biol Pharm Bull. 2002;25(12):1647-50.
- Kodama N, Komuta K, Nanba H. Effect of Maitake (Grifola frondosa) D-Fraction on the activation of NK cells in cancer patients. J Med Food. 2003;6(4):371-7. PMID: 14977447
- “Vitamin D” In: Brody T. Nutritional Biochemistry, 2nd edition. San Diego, Ca: Academic Press; 1999:565-585.
- Berube S, Diorio C, Verhoek-Oftedahl W, Brisson J. Vitamin D, calcium, and mammographic breast densities. Cancer Epidemiol Biomarkers Prev. 2004 Sep;13(9):1466-72.
- Banwell CM, O'Neill LP, Uskokovic MR, Campbell MJ. Targeting 1alpha,25-dihydroxyvitamin D3 antiproliferative insensitivity in breast cancer cells by co-treatment with histone deacetylation inhibitors. J Steroid Biochem Mol Biol. 2004 May;89-90(1-5):245-9. PMID: 15225779
- Weitsman GE, Ravid A, Liberman UA, Koren R. Vitamin D enhances caspase-dependent and independent TNF-induced breast cancer cell death: the role of reactive oxygen species. Ann N Y Acad Sci. 2003 Dec;1010:437-40. PMID: 15033766
- Walaszek Z, Szemraj J, Narog M, Adams AK, Kilgore J, Sherman U, Hanausek M. Metabolism, uptake, and excretion of a D-glucaric acid salt and its potential use in cancer prevention. Cancer Detect Prev. 1997;21:178-190.
- Walaszek A, Hanausek M Sherman U, Adams AK. Antiproliferative effect of dietary glucarate on the Sprague-Dawley rat mammary gland. Cancer Lett. 1990;49:51-57.
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