Perhaps selenium can prevent hereditary breast cancer

May 30, 2005

Women with a genetic tendency towards breast cancer have unstable chromosomes. Studies now show that these chromosomes can be stabilized by taking selenium supplements.
About every twenty cases of breast cancer are due to inheritance. Most often, the cause is an innate mutation in the so-called BRCA1 gene, which, under normal circumstances, repairs damage to chromosomes.

If you carry this mutation, you already have a high risk of breast cancer: Approximately 60% will get the disease before they reach 50, and approximately 85% will get it before they reach 70. At the same time, the risk of ovarian cancer is no less than 60%.

It is a despairing situation to be born with this mutation, which presents the affected with difficult decisions. Some prefer to prevent the cancer by having their breasts and ovaries removed at a young age, while others wait and see if they are among the unlucky ones. Those affected must at least think about having the children they want at a young age if they want to retain the opportunity to breastfeed. There is no certainty as to when the disease will strike.

Now, however, a highly interesting Polish study suggests that the risk can be significantly reduced with a simple supplement of selenium. The supplement drastically reduces the frequency of chromosomal damage in women with the congenital defect. This can, if the results hold, buy the vulnerable women time and reduce their risk of instability in the protective chromosomes.

The experiment was carried out at the Pomeranian Academy of Medicine in Szczecin. It was about measuring the amount of mutations – so-called chromosome breaks – on white blood cells, which in the laboratory were exposed to “chemical radiation” in the form of the chemotherapy drug bleomycin.

Two experiments were performed. In one, chromosome breaks were compared in 26 women with and 26 women without the congenital defect. In the first, 0.59 fractures per cell were measured, while women without the defect had only 0.39.

35 other women, all of whom were carriers of the mutation, now participated in the second trial. Half of them received a daily supplement of approx. 280 mcg selenium a day, after which they had blood samples taken after 1-3 months, so that their blood cells could also be exposed to bleomycin. The result was almost exactly as in the first experiment: In the blood cells of the women who did not receive selenium, 0.63 chromosome breaks occurred per cell, while those who received the selenium had only 0.40 fractures per. cell.

In other words, women with the inherited mutation could increase the stability of their chromosomes to normal with something as simple as a daily selenium supplement. The question then is how this is to be interpreted. Does this mean that they also had their cancer risk reduced?

There are many indications of this, but one cannot be sure. Researchers have concluded that hereditary breast cancer is due in part to unstable chromosomes. Others have found that breast cancer patients have clearly more chromosomal abnormalities in their white blood cells than healthy ones. In addition, several experiments have shown a correlation between the susceptibility to cancer in general and the level of chromosome rupture.

In addition, a study of 3,812 workers who were exposed to mutation-promoting substances showed that those who had the most chromosomal abnormalities were also most likely to get cancer later on. The clues are many.

Selenium has an antioxidant effect and has been shown to be strongly anti-cancer in several trials. As the soil in Poland (just like Denmark) is very low in selenium, the researchers believe that a similar experiment in other countries could give a different result.

The participants received the equivalent of approx. three regular selenium tablets with organic selenium a day. It is a dose that certainly does not exceed what is allowed.

By: Vitality Council

References:
Kowalska E. et al. Increased rates of chromosome breakage in BRCA1 carriers are normalised by oral selenium supplementation. Cancer Epidem Biomarkers Prev 2005;14(5):1302-6.

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Perhaps Prostate Cancer may be a Rarity in the Future

April 1, 2005

Every forth man lives with a highly increased risk of getting cancer of the prostate, the next most frequent cause to cancer deaths in men. It does not have to be like that. Exactly these exposed men could easily decrease their risk to a tenth.

Researchers from Harvard University in Boston have published a landmark study. It strongly suggests that most cases of cancer in the prostate are due to lack of balance in the body’s defense against free oxygen radicals. And most importantly: This balance can be restored with antioxidants – especially with selenium, but also vitamin E and the red dye of the tomatoes, lycopene. Prostate cancer can thus become a rare disease.

The imbalance occurs especially in men who get too little selenium and who, for hereditary reasons, have a particularly effective antioxidant enzyme (manganese-containing SOD) in their mitochondria. The mitochondria are the cells’ internal energy factories, which are worn down by free oxygen radicals with age. This wear and tear, parenthetically noted, is believed to be a very significant cause of aging and age-related diseases.

One would therefore think that it was an advantage to have a particularly effective antioxidant enzyme in one’s mitochondria. But very often it is not. The SOD enzyme transforms free oxygen radicals into the less risky hydrogen peroxide, but this creates a new problem: the hydrogen peroxide must also be removed, since it also causes harmful oxygenation. The removal requires an enzyme (glutathione peroxidase), the quantity of which depends on the supply of selenium.

The more free oxygen radicals (e.g. from smoking) that need to be neutralized and the more efficient the SOD enzyme is, the more harmful hydrogen peroxide accumulates and the greater the need for selenium.

Balance in things
The Harvard study is part of a study of approx. 15,000 American doctors who have been followed since 1982. Around 1990, 275 of them had developed serious prostate cancer, and it was those who were primarily found interesting.

By: Vitality Council

References:
1. Haojie Li et al. : Manganese superoxide dismutase polymorphism, prediagnostic antioxidant status, and risk of clinical significant prostate cancer. Cancer Res. 2005;65:2498-2504.
2. Woodson et al. Manganese superoxide dismutase (MnSOD) polymorphism, α-tocopherol supplementation and prostate cancer risk in the α-Tocopherol, β-Carotene Cancer Prevention Study. Cancer Causes Control 2003;14:513-8
3. Niels Hertz. Selen – et livsvigtigt spormineral. Forlaget Ny Videnskab 2002.

www.aacr.org/cncrrea.htm
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Selenium, Research references

January 1999

  1. Bruce A et al. The effect of selenium and vitamin E on glutathione peroxidase levels and subjective symptoms in patients with arthrosis and rheumatoid arthritis, in Proc N Z Workshop on Trace Elements in N Z. Dunedin, U. of Otago, 1981: 92.
  2. Chen X, Xiaoshu, Chen X et al. Selenium in biology and medicine. New York: AVI/Van Nostrand Reinhold. 1987: p 589-607.
  3. Clark LC. The epidemiology of selenium and cancer. Fed Proc 1985; 44: 2584-2589.
  4. Clark L, Combs GF Jr, Turnbull BW et al. Effects of selenium supplementation for cancer prevention in patients with carcinoma of the skin. JAMA 1996.
  5. Constans J, Pellegrin JL, Sergeant C, et al. Serum selenium predicts outcome in HIV infection. J AIDS Human Retrovirol 10:392, 1995.
  6. Delmas-Beauvieux M-C, Peuchant E, Couchouron A, et al. The enzymatic antioxidant system in blood and glutathione status in human immunodeficiency virus (HIV)-infected patients: Effects of supplementation with selenium or carotene. Am J Clin Nutr 64:101-7, 1996.
  7. Fletcher MP, Gershwin ME, Keen CL et al. Trace element deficiences and immune responsiveness in humans and animal models. In: Chandra RK, ed. Nutrition and immunology. New York: Alan R, Liss. p 215-239, 1988.
  8. Gebre-Medhin M et al. Selenium supplementation in X-linked muscular dystrophy. Effects on erythrocyte and serum selenium and on erythrocyte glutathione peroxidase activity. Acta Paediatr Scand 74;6:886-90, 1985.
  9. Glover JR. Proceedings of the symposium on selenium-tellurium environments. Pittsburgh: Industrial Health Foundation. 1976: p 279-292.
  10. Hinks LJ, Inwards KD, Lloyd B, Clayton BE. Body content of selenium in coeliac disease. Br Med J Clin Res 288:1862-3, 1984.
  11. Jackson ML. Selenium. Present status and perspectives in biology and medicine. Clifton, NJ: Humana Press. 1988: p 13-21.
  12. James S et al. Effekter av selenvitamin E-behandling till kvinnor med lång variga arbetsrelaterade nack-och skuldersmärtor. En dubbelblindstudie. Läkaresällskapets Riksstämma, 1985.
  13. Jameson S et al. Pain relief and selenium balance in patients with connective tissue disease and osteoarthrosis: A double-blind selenium tocopherol supplementation study. Nutr Res Suppl 1: 391-7, 1985.
  14. Juhlin L et al. Blood glutathione-peroxidase levels in skin diseases: Effect of selenium and vitamin E treatment. Acta Derm Venereal (Stockh) 62; 3: 211-4, 1982.
  15. Karakucuk S et al. Selenium concentrations in serum, lens and aqueous humor of patients with senile cataract. Acta Ophthalmol Scand 73:323-32, 1995.
  16. Kok FJ et al. Decreased selenium levels in acute myocardial infarction. JAMA 261;8:1161-4, 1989.
  17. Korpela H et al. Effect of selenium supplementation after acute myocardial infarction. Res Commun Chem Pathol Pharmacol 65:249-52, 1989.
  18. Kose K et al. Plasma selenium levels in rheumatoid arthritis. Biol Trace Elem Res 53: 51-6, 1996.
  19. L’Abbe M, Fischer W, Trick K et al. Dietary Se and tumor glutathione peroxidase and superoxide dismutase activities. J Nutr Biochem 1991; 2: 430-436.
  20. Levander OA. A global review of human selenium nutrition. Ann Rev Nutr 1987; 7: 227-250.
  21. Levander OA. Trace substances in environmental health – 23. Springfield: University of Missouri. 1990: p 11-19.
  22. Levander, OA, Burk, RF. Selenium. In. Present knowledge in nutrition. 7th edn. Washington, DC: Nutrition Foundation. 1996: p 320-328.
  23. Longnecker GF. Nutrition and cancer prevention: investigating the role of micronutrients. New York: Marcel Dekker. 1989: p 389-420.
  24. Macpherson A, Scott R, Yates R. The Effect of Selenium Supplementation in Sub-Fertile Males. (Abstract), 8th International Conference on Trace Element Metabolism in Man and Animals, 1993.
  25. Moore JA et al. Selenium concentrations in plasma of patients with arteriographically defined coronary atherosclerosis. Clin Chem 30:1171, 1984
  26. Munthe E, Aaseth J. Treatment of Rheumatoid Arthritis with Selenium and Vitamin E. Scan J of Rheumatol 53 (suppl.): 103, 1984.
  27. Oster O et al. The serum selenium concentration of patients with acute myocardial infarction. Ann Clin Res 18;1:36-42, 1986.
  28. Overad K, Thorling EB, Bjerring P, Ebbesen P. Selenium inhibits W-light-induced skin caronogenesis in hairless mice. Cancer Lett 1985; 27: 163-170.
  29. Peretz A, Nève J, Famaey J. Selenium in rheumatic diseases. Semin Arthritis Rheum 20: 305-16, 1991.
  30. Peretz A, Nève J, Duchateau J, Famaey JP. Adjuvant treatment of recent onset rheumatoid arthritis by selenium supplementation: Preliminary observations. Br J Rheumatol 31: 281-6, 1992.
  31. Robinson MF et al. Effect of daily supplements of selenium on patients with muscular complaints in Otago and Canterbury. N Z Med J 93:289-292, 1981.
  32. Salonen JT et al. Association between cardiovascular death and myocardial infarction and serum selenium in a matched-pair longitudinal study. Lancet ii:175-9, 1982
  33. Salonen JT, Alfthan G, Huttunen JK, Puska P. Association between serum selenium and the risk of cancer. Am J Epidem 1984; 120: 342-349.
  34. Salonen JT et al. Interactions of serum copper, selenium, and low density lipoprotein cholesterol in atherogenesis. Br Med J 302:756-60, 1991.
  35. Schrauzer GN, Sacher J. Selenium in the maintenance and Therapy of HIV-infected patients. Chem Biol Interact 91:199-205, 1994.
  36. Shamberger RJ, Frost DV. rossible protective effect of selenium against human cancer. Can Med Assoc J 1969; 100: 682.
  37. Shamberger RJ. Biochemistry of selenium. New York: Plenum. 1983.
  38. Sklodowska M, Wasowicz W, Gromnadzinska J, et al. Selenium and vitamin E concentrations in plasma and erythrocytes of angina pectoris patients. Trace Elem Med 8:113-17, 1991.
  39. Stead NW et al. Selenium Se balance in the dependent elderly. Am J Clin Nutr 39:677, 1984.
  40. Stone WL et al. Effects of dietary selenium and vitamin E on plasma lipoprotein cholesterol levels in male rats. Ann Nutr Metab 30:94-103, 1986.
  41. Suadicani P, Hein H, Gyntelberg F. Serum selenium concentration and risk of ischaemic heart disease in an prospective cohort study of 3000 males. Atherosclerosis 96:33-42, 1992.
  42. Sunde RA. Molecular biology of selenoproteins. Ann Rev Nutr 1990; 10: 451-474.
  43. Sword J, Pope A, Hoekstra W. Endotoxin and lipid peroxidation in vitro in selenium- and vitamin E-deficient and -adequate rat tissues. J Nutr 1991; 121: 258-264.
  44. Tarp U et al. Low selenium level in severe rheumatoid arthritis. Scand J Rheumatol 14: 97, 1985.
  45. Tarp U et al. Selenium Treatment in Rheumatoid Arthritis. Scandinavian J of Rheumatol 14: 364-8, 1985.
  46. Vanderpas JB, Contempre B, Duale NL et al. Iodine and selenium deficiency associated with cretinism in northern Zaire. Am J Clin Nutr 1990; 52: 1087-1094.
  47. Van Rij AM et al. Selenium deficiency in total parenteral nutrition. Am J Clin Nutr 32:2076-85, 1979.
  48. Virtamo J et al. Serum selenium and the risk of coronary heart disease and stroke. Am J Epidemiol 122:276-82, 1985.
  49. Winnefeld K, Dawczynski H, Schirrmeister W et al. Selenium in serum and whole blood in patients with surgical interventions. Biological Trace Element Res 1995; 50: 149-155.
  50. Wright JV, Ogle DJ, Hoare L. Improvement of vision in macular degeneration associated with intravenous zinc and selenium therapy: two cases. J Nutr Med 1:133-8, 1990.
  51. Yang GQ Wang SZ, Ahou RH, Sun SZ. Endemic selenium intoxication of humans in China. Am J Clin Nutr 1983- 37: 872-881.
  52. Yu SY et al. Chemoprevention trial of human hepatitis with selenium supplementation in China. Biol Trace Elem Res 21; 1-2:15-22, 1989.
  53. Zazzo JF, Chalas J, Lafont A, et al. Is nonobstructive cardiomyopathy in AIDS a selenium deficiency-related disease? Letter. JPEN J Parenter Enteral Nutr 12; (5):537-8, 1988.
  54. Zielonka E et al. Sulfur and selenium levels in the blood of patients with rheumatoid arthritis and ankylosing spondylitis. Reumatologia 20; 3-4: 217-20, 1982.
  55. Örndahl G et al. Myotonic dystrophy and selenium. Acta Med Scand 211:493-9, 1982.
  56. Örndahl G et al. Selenium therapy of myotonic dystrophy. Acta Med Scand 213;3:237-9, 1983.
  57. Örndahl G et al. Myotonic dystrophy treated with selenium and vitamin E. Acta Med Scand 219:409-44, 1986.

 

Sources:
Joseph E. Pizzorno Jr., Michael T. Murrey & Melvyn R. Werbach.