Health Conditions

Would you like to get valuable condition related information?

New Study Suggest Quercetin Supplementation May Reduce Risk Of Colon Cancer

Take FREE Health Assessment- Instant Results

Quercetin is a flavonoid that serves as the backbone for many other flavonoids in nature, including the citrus flavonoids rutin, quercitin, and hesperidin.  These derivates differ from Quercetin in that they have sugar molecules attached to their Quercetin backbone.  Experimental studies reveal that many medicinal plants owe much of their biological activity to their high Quercetin content.  Abundant evidence indicates that quercetin supplementation provides anti-inflammatory effects, may inhibit the formation and/or progression of cataracts, and has anti-tumor properties. A recent human trial showed that quercetin supplementation (in conjunction with curcumin – another natural supplement) reduced colon cancer incidence in high-risk subjects, which is discussed at the end of this review.

Anti-Inflammatory Effectscancer_400

Quercetin inhibits the manufacture and release of histamine and other allergic/inflammatory mediators, which gives Quercetin supplementation application in a variety of inflammatory and allergic reactions (arthritis, joint inflammation, asthma, hay fever, lupus, etc.) It also demonstrates impressive anti-inflammatory and antioxidant properties, and like some other flavonoids (e.g. genistein, diadzein), appears to possess phytoestrogen effects.  In one human trial, Quercetin supplementation demonstrated improvement in prostatitis, with 67% of patients experiencing significant improvement in the Quercetin group compared to only 20% of patients reporting improvement in the placebo group.  This benefit may be due to its phytoestrogen activity and/or its anti-inflammatory properties.

Inhibits Formation of Diabetic Cataracts 

Quercetin inhibits the aldose reductase enzyme, which converts glucose into sorbitol.  Sorbitol build-up in the lens of the eye (secondary to diabetes and hyperglycemia) is involved in the development of cataracts. Elevated sorbitol may also contribute to the development of diabetic neuropathy and retinopathy. Thus, Quercetin may be beneficial in diabetes management for a number of reasons. Animal studies reveal that Quercetin effectively delays the onset of cataracts in diabetic animals

Anti-Tumor Effects

Many flavonoids inhibit tumor formation, but Quercetin has demonstrated a very consistent effect in this regard.  Under experimental conditions, Quercetin demonstrates a significant antiproliferative effect in regards to squamous cell carcinoma, leukemia, and cancers of the breast, ovaries, colon, rectum and brain. It is thought that Quercetin down-regulates enzymes that control the rate of cellular division (i.e., protein kinase, DNA-topoisomerase, ornithine decarboxylase), in addition to its mild phytoestrogen effects. Under experimental conditions, its phytoestrogen effects have been shown to inhibit the proliferation of human breast cancer cells in test tube experiments.

Recent Studies Indicate That Quercetin Supplementation Decreases Colon Cancer Risk

Experimental evidence has shown the mechanism of action through which quercetin can protect against colon cancer development in a number of experimental and animal studies:

  • slows colon cancer cell replication
  • induces programmed cell death of cancer cells (apoptosis)
  • encourages normal differentiation of colon cells and colon cancer cells
  • acts as an antioxidant and anti-inflammatory agent

The addition of quercetin to cultured human colon cancer cells (Caco-2 cells: human adenocarcinoma colon cancer cells) inhibited the ability of the colon cancer cells to replicate. After exposure to quercetin, cell replication rates decreased to 51.3% compared to cancer cells not exposed to quercetin. Some animal studies have shown that oral administration of quercetin reduces the development of colon cancer in animals exposed to cancer-causing agents known to induce colon cancer development (animals given the quercetin showed significantly less cancers than those not given quercetin). As well, experimental studies indicate that quercetin can cause undifferentiated cancer cell lines to differentiate and has been shown to protect against hydrogen peroxide induced DNA strand breaks in human adenocarcinoma cells (Caco-2 cells).

A study in The European Journal of Nutrition (M.J. van Erk et al/2005) demonstrated that quercetin inhibited proliferation of human colonic adenocarcinoma cells (Caco-2 cells) via a number of biological actions. These include down-regulation expression of cell cycle genes (e.g., CDC6, CDK4 and cyclin D1), down-regulation of cell proliferation and induced cell cycle arrest.

The strong experimental and animal research cited above led researchers to test whether or not quercetin could prevent colon cancer in human subjects, who are known to be at high risk for colon cancer development. Individuals with a hereditary condition known as familial adenomatous polyposis are known to have a high risk of developing colon cancer, as they produce numerous polyps in the large bowel, which are prone to undergoing conversion to malignancy. In a study involving 5 patients with familial adenomatous polyposis (FAP: an autosomal-dominant disorder characterized by the development of hundreds of colorectal adenomas and eventual colorectal cancer) and prior colectomy (4 with retained rectum and 1 with an ileal anal pouch), supplementation with curcumin and quercetin reduced the number and size of ileal and rectal adenomas. The patients received oral supplementation with 480 mg curcumin and 20 mg quercetin, three times a day.

At treatment end, the number and size of polyps decreased in all five patients, with a 60.4% mean decrease in the number of polyps and a 50.9% mean decrease in the size of polyps. Additionally, minimal adverse side effects and no laboratory abnormalities were observed in the patients during the treatment period. Thus, the findings of this study indicate that supplementation with curcumin and quercetin may reduce the number and size of ileal and rectal adenomas in patients with FAP and may help to prevent colon cancer development in general.

Curcumin was tested with quercetin in this study because it also shares many of the same anti-colon cancer properties as quercetin, according to experimental and animal studies. Curcumin is a constituent of the spice turmeric and can be found in many supplements that are used to reduce joint inflammatory condition.

In regards to the preventive dosages of quercetin, large bowel concentrations of quercetin can reach 100 micromoles in the intestinal lumen after ingestion of a quercetin supplement (250-500 mg). Studies show that the addition of only 50 micromoles to human adenocarcinoma cells (Caco-2 cells) can inhibit their proliferation by more than 50%.

Dosage

  1. Anti-Inflammatory/Anti-Allergy:  as a single agent; 200-400 mg, three times per day.  Combinations of bromelain and Quercetin have been shown to potentiate or enhance each other’s anti-inflammatory activity.  The amount of bromelain should be equal to the amount of Quercetin. Bromelain also enhances the absorption of Quercetin.
  2. Diabetes (neuropathy or cataract protection):  consider 200-400 mg (three times per day).
  3. Colon Support: The study by Cruz-Correa M and Shoskes DA suggest that supplementation with 60 mg of quercetin and 1440 mg of curcumin, per day may reduce risk of colon cancer

Colon Cancer:

Colon cancer is the second leading cause of cancer death in North America, after lung cancer.  Studies reported in the Journal of the National Cancer Institute indicate that 70-90% of all colon cancer cases are produced by faulty dietary and lifestyle factors. In addition to quercetin and curcumin supplementation, a number of other lifestyle practices are associated with decreased risk of colon cancer, some of which include:

  • Low animal fat diet
  • Calcium Intake above 1200 mg per day
  • Blood levels of Vitamin D above 85 nmol/L
  • Regular Exercise
  • Alcohol consumption below two drinks per day, on average
  • Reduced intake of foods containing nitrate salts, heterocyclic amines, and polycyclic aromatic hydrocarbons (from smoked, BBQ, charred and pan-fried meats)
  • High intake of cruciferous vegetables and dietary fibre
  • Selenium Supplementation at 100-200 mcg per day (which can be from a multiple vitamin and mineral)
  • Folic acid intake of 400 mcg per day from a supplement (can be from a multiple vitamin and mineral supplement)
  • Intake of omega-3 fats achieving at least one gram per day
  • Higher than average intakes of vitamin C and supplementation with vitamin E (at least 100 IU per day)
  • Not smoking

Adverse Side Effects and Toxicity of Quercetin

Animal studies demonstrate that Quercetin is extremely non-toxic and non-carcinogenic.  In rare cases, allergic reactions to Quercetin can occur in humans.

Quercetin Drug-Nutrient Interactions of Importance

  1. Estradiol (found in oral contraceptives and hormone replacement therapy)

    Quercetin may slow down the detoxification of estradiol by liver enzymes.  There are no human reports of Quercetin potentiating the effects of estradiol through this mechanism at this time.

  2. Felodipine

    Felodipine is a calcium channel blocker used in the treatment of congestive heart failure, hypertension and Raynaud’s Syndrome.  Test tube studies indicate that Quercetin inhibits the enzyme in the liver that is responsible for the breakdown of felodipine.  This may result in higher, more potentially dangerous levels of felodipine in the bloodstream, although no human reports of adverse effects have been reported to date.

References

  1. Murray M. Encyclopedia of Nutritional Supplements. Rocklin, CA: Prima Publishing; 1996.  p. 320-31.
  2. Beyer-Meyers A, et al.  Diminished sugar cataractogenesis by quercetin.  Exp Eye Res 1979; 28(6): 709-16
  3. Chaudry PS, et al.  Inhibition of human lens aldose reductase by flavonoids, sulindac, and indomethacin.  Biochem Pharmacol.  1983; 32: 1995-98 
  4. Havsteen B.  Flavonoids, a class of natural products of high pharmacological potency.  Biochem Pharmacol 1983;32:1141-8.
  5. Middleton E.  The flavonoids.  Trends Pharmaceut Sci 1984;5:334-8.
  6. Ferrandiz ML, Alcaraz MJ.  Anti-inflammatory activity and inhibition of arachidonic acid metabolism by flavonoids.  Agents Action 1991;32:283-7.
  7. Middleton E, Drzewiedi G.  Flavonoid inhibition of human basophil histamine release stimulated by various agents.  Biochem Pharmacol 1984;33:3333-8.
  8. Middleton E, Drzewieki G.  Naturally occurring flavonoids and human basophil histamine release.  Int Arch Allergy Appl Immunol 1985;77:155-7.
  9. Amella M, Bronner C, Briancon F, Haag M, Anton R, Landry Y.  Inhibition of mast cell histamine release by flavonoids and bioflavonoids.  Planta Medica 1985;51:16-20.
  10. Pearce F, Befus AD, Bienenstock J.  Mucoal mast cells, III.  Effect of quercetin and other flavonoids on antigen-induced histamine secretion from rat intestinal mast cells.  J Allergy Clin Immunol 1984;73:819-23.
  11. Busse WW, Kopp DE, Middleton E.  Flavonoid modulation of human neutrophil function.  J Allergy Clin Immunol 1984;73:801-9.
  12. Yoshimoto T, Furukawa M, Yamamoto S, Horie T, WatanabeKohno S.  Flavonoids: Potent inhibitors of arachidonate 5-lipoxygenase.  Biochem Biophys Res Common 1983;116:612-8.
  13. Chaundry PS, Cambera J, Juliana HR, Varma SD.  Inhibition of human lens aldose reductase by flavonoids, sulindac and indomethacin.  Biochem Pharmacol 1983;32:1995-8.
  14. Varma SD, Muzuno A, Kinoshita JH.  Diabetic cataracts and flavonoids.  Science 1977;195:87-9.
  15. Elangovan V, et al.  Studies on the chemopreventative potential of some naturally-occurring biovlavonoids in 7,12-dimethylbenz(a)anthracene-induced carcinogens in mouse skin.  J Clin Biochem Nutr 1994;17:153-60.
  16. Verma AK, Johnson JA, Gould MN, Tanner MA.  Inhibition of 7,12-dimenthylbenz(a)anthracene and N-nitrosomethyl urea induced rat mammary cancer by dietary flavonol quercetin. Cancer res 1988;48:5754-5758.
  17. Stavric B.  Quercetin in our diet: from potent mutagen to probable anticarcinogen.  Clin Biochem 1994;27:245-8.
  18. Larocca LM, Giustacchini M, Maggiano N, Ranelletti FO, Piantelli M, Alcini E et al.  Growth-inhibitory effect of quercetin and presence of type II estrogen binding sites in primary human transitional cell carcinomas.  J Urol 1994;152:1029-33.
  19. Castillo MH, Perkins E, Campbell JH, et al.  The effects of the bioflavonoid quercetin on squamous cell carcinoma of head and neck origin.  Am J Surg 1989: 351-5
  20. Kuo SM.  Antiproliferative potency of structurally distinct dietary flavonoids on human colon cancer cells.  Cancer Letter 1996;110:41-8.
  21. Tarayre JP, Lauressergues H.  Advantages of a combination of proteolytic enzymes, flavonoids and ascorbic acid in comparison with non-steroid anti-inflammatory agents.  Arzneim Forsch 1077;27:1144-9.
  22. Hirono I, Ueno I, Hosaka S, Takanashi H, Matsushima T, Sugimura T et al. Carcinogenicity examination of quercetin and rutin in ACI rats.  Cancer Lett 1981;13:15–21.
  23. Kato K, et al.  Lack of promotive effect of quercetin on methlazoxy acetate carcinogenesis in rats.  J Toxicol Sci 1984;9:319-25.
  24. Kato K, et al.  Absence of initiating activity by quercitin in the rate liver.  Ecotoxicol Environ Safety 1985;10:63-9.
  25. Healthnotes online. Healthnotes Inc, 2000.
  26. Doll R, Peto R: The causes of cancer: Quantitative estimates of avoidable risks of cancer in the United States today.  J Natl Cancer Instit.., 66:1191-1308, 1981
  27. Willet, W. Estimates of cancer deaths avoidable by dietary change. J Natl Cancer Instit., 1996; 86, 14: 948).
  28. Van Erk MJ; Roepman P; van der Lende TR; et al. Integrated assessment of multiple gene expression analysis of quercetin bioactivity on anticancer-related mechanisms in colon cancer cells in vitro. Eur J Nutr. 44: 143-156. 2005
  29. Su CC: Chen GW; Lin JG; Wu LT; Chung JG. Curcumin inhibits cell migration of human colon cancer colo 205 cells through the inhibition of nuclear factor kappa B /p65 and down-regulates cyclooxygenase-2 and matrix metalloproteinase-2 expressions. Anticancer Research [Anticancer Res] 2006 Mar-Apr; Vol. 26 (2A), pp. 1281-8.
  30. Cruz-Correa M, Shoskes DA, et al. Combination Treatment With Curcumin and Quercetin of Adenomas in Familial Adenomatous Polyposis. Clin Gastroenterol Hepatol., 2006, Jun 4

 

Related Articles