by Dr. James Meschino on 15 March 2021 in Diet, Cancer

Tags:  lifestyle, Nutrients 

How Diet And Prostate Cancer linked to each other?

Introduction

Before focusing on Diet and Prostate cancer,the studies revealed that  Prostate cancer incidence increased steadily from 1981 to 1989, with a steep increase in the early 1990’s, followed by a decline. Incidence rates were forecasted to remain stable through the year 2001.

However, the exaggerated rate of increase in the early 1990’s was transient and likely a result of increased early detection of preclinical prostate cancer due to widespread implementation of the new PSA (prostate specific antigen) blood-screening test.

Nevertheless, prostate cancer remains the most common cancer in North American men, as well as in other Western countries, and is the second leading cause of cancer death in males.(1)

As reported in the Journal of the National Cancer Institute, as much as 75% of prostate cancer may be prevented if men followed more prudent nutritional practices, many of which will be outlined in this review. (2)

In Japan the incidence of prostate cancer is 80% lower than in North America and much of the Western world. Low rates are also found in Africa and Eastern Europe. Migration studies reveal that when men relocate from a low- to high-risk region of the world and abandon their traditional dietary patterns, their incidence of prostate cancer rises to approach that of North American men. (3,4)

In recent years a number of nutritional factors and bioactive compounds have been identified that shows  strong links between diet and prostate cancer.

In fact, in the past year (2001) published data from the Harvard Alumni Study revealed that men with moderate liquor consumption (3 drinks per week to 3 drinks per day) show a 61-67% increased risk of developing prostate cancer compared to men who never or infrequently consumed alcohol.

Wine and beer did not appear to be as hazardous as liquor, however men initiating alcohol consumption of any kind between 1977 and 1988 had a twofold increased risk of prostate cancer compared to men with almost no alcohol consumption at both evaluation dates (after controlling for other confounding variables).

This study followed 7612 Harvard alumni (mean age - 66.6 years) from 1988 through 1993. (5)

Also in 2001, the study by K.T. Bogen and G.A. Keating provided evidence that higher intakes of heterocyclic amines among the U.S. Black population, especially from pan-fried meats, may partially explain the twofold increase in prostate cancer in this group, as U.S. Blacks were shown to consume approximately two- and approximately three-fold more heterocyclic amines at ages less than 16 and over 30, respectively.

Heterocyclic amines are potent mutagens that increase the rates of colon, mammary, prostate and other cancers in bioassay rodents. (6)

In the journal Oncogene (2001), S.R. Chinni et al, provided strong evidence to show that the indole ring structures present in cruciferous vegetables may play an important role in the prevention of prostate cancer.

This study demonstrated that indole rings (indole-3-carbinols) can inhibit the growth of PC-3-type human prostate cancer cells by arresting their cell division cycle and promote their demise through apoptosis (programmed cell death).

They conclude that indole-3-carbinols may be an effective chemopreventive or therapeutic agent against prostate cancer. Previously, similar findings have argued for the ingestion of indole-3-carbinols as a means to prevent breast cancer in women. (7)

As well, a link between vascular disease and increased risk of prostate cancer has been reported recently suggesting that heightened central sympathetic stimulation, which can lead to elevated blood pressure and heart rate, also may over-stimulate the androgen activity of prostate cells. Increased androgen activity is strongly linked to prostate cancer.

Thus, heart rate and blood pressure may represent indirect markers of sympathetic stimulation of androgen activity on the prostate.

In support of this model, recent data (2001) from the Cardiovascular Health Study (n=2442 men) demonstrated that men with a resting heart rate equal to or greater than 80 beats per minute had a 60% greater chance of developing prostate cancer, during the 5.6-year follow-up period, compared to men with a resting heart rate of less than 60 beats per minute, an indirect indicator of cardiovascular fitness and lower sympathetic tone. (8)

In addition to these recent publications, a vast amount of prior evidence indicates that risk of prostate cancer is largely determined by nutritional and other lifestyle factors, as well as age-related changes that occur in the prostate gland.

Incredibly, even undesirable age-related changes to the prostate may be preventable and reversible through nutrition and supplementation practices, including changes that lead to prostate enlargement (benign prostatic hyperplasia), which affects 50-60% of men by age 40-59 and 80% of men by age 80.

Thus, nutritional support for the prostate gland is considered to be an important anti-aging intervention to preserve the health and function of this gland and in the prevention and treatment of prostate disease. (9,10)

This review brings to light the evidence-based research that should prompt all health practitioners to counsel their male patients on the importance of diet and prostate cancer in lifelong prostate health.

Does Age–Related Change Is Linked to Prostate

As men age (by age 40), the prostate gland tends to accelerate the rate at which it converts testosterone to dihydrotestosterone (DHT). The build-up of DHT in prostate cells stimulates them to divide and multiply at a faster rate.

This results in more prostate cells (more prostate mass) and the potential for prostate enlargement and other problems. As the prostate enlarges under the influence of DHT, men often notice symptoms such as reduced strength of their urine stream, more frequent urination, repeated nighttime urination, bladder urgency and related symptoms. (10)

More rapid cell division rates also increase the chances of forming cancerous DNA mutations. In fact, DHT is known to promote the spread of existing prostate cancer and males born with the genetic inability to synthesize DHT are virtually immune from developing prostate cancer in their lifetime.

There is no question that DHT is linked to prostate cancer and prostate enlargement in a number of ways. (11,12) The encouraging news is that specific nutrients and natural bioactive compounds in foods and certain supplements have been shown to block the conversion of testosterone to DHT and exert other protective effects within the prostate gland.

As such, the consumption of these products at the correct dosage and/or standardized grade have been shown to be effective in the treatment of enlarged prostate problems, and some of these natural agents are associated with the prevention of prostate cancer, and more recently, in the treatment of prostate cancer. (13)

What are the Nutrients That Block The Build Up Of DHT?

There are several known natural agents that can effectively block the build-up of DHT within the prostate gland. The primary ones include the standardized grade of saw palmetto, pygeum africanum, beta-sitosterol, soy isoflavones and stinging nettle (urtica dioica).

Numerous studies have shown that the fatty acids and sterols present in saw palmetto block the build-up of DHT and exert other favourable effects on prostate health.

Saw Palmetto extract is a proven therapy for enlarged prostate problems and has recently been used in trials with prostate cancer patients, yielding impressive results in helping to contain the disease and lower PSA levels by more than 75% in many cases.

For the prevention and treatment of benign prostatic hyperplasia (BPH) the usual dose is 160 mg, twice daily, of saw palmetto extract (std to 90% fatty acids and sterols) or 320 mg, twice per day, of a standardized grade containing 45% fatty acids and sterols.

Pygeum Africanum contains active compounds known as triterpenes, which have also been shown to be effective in the treatment of enlarged prostate problems in numerous human studies. The usual dose of Pygeum for the prevention and treatment of BPH is 100-200 mg per day (std. to 12-14% triterpenes).

In recent years, prestigious medical journals such as the Lancet and the British Journal of Urology have published research papers demonstrating that beta-sitosterol (found in saw palmetto, soy products and in other plant foods) at 20 mg, three times per day, or 65 mg, twice per day, is also extremely effective in reversing BPH.

Contained within soy products, and including soy extract, are several important isoflavones, the most important of which include genistein and diadzein. These isoflavones directly inhibit the build up of DHT and exhibit many other biological properties that are related to the prevention of prostate disease and prostate enlargement as men age.

Soy isoflavones have been shown to induce apoptosis (programmed cell death) of human prostate cancer cell lines, decrease androgen stimulation to the prostate gland, slow the cell division

rate of prostate cells and prostate cancer cells, and reduce the conversion of androstenedione to estrone hormone in adipose tissue by acting as an aromatase enzyme inhibitor.

All of these physiological effects are known to reduce prostate cancer development and/or arrest prostate cancer growth.  As previously stated, in Japan, where soy isoflavone intake is high (avg. 50 mg per day), prostate cancer incidence is 80% lower than in North America.

The herbal agent stinging nettle, (urtica dioica) also enjoys a reputation as a natural agent that has consistently been shown to reverse prostate enlargement in European studies. Prostate combination formulas often include 20-60 mg of stinging nettle as part of the complex. (14-34)

How Antioxidants Assist Prostate?

Studies indicate that prostate cancer may also arise from free radical damage to prostate cells, converting them into mutated, cancer cells. Evidence is very strong to suggest that the antioxidant lycopene (derived from tomatoes), plays an essential role in protecting prostate cells from free radical damage.

Lycopene is known to concentrate in the prostate gland and its fluids, at levels much higher than are found in serum. As such, it has been shown to be a tissue-specific antioxidant in prostate health. 

Human studies such as the Physicians’ Health Study and the Health Professionals’ Follow Up Study have shown a striking correlation between higher lycopene blood levels and/or intake levels (6 mg per day), and a marked reduction in prostate cancer development (as much as a 40% reduction).

Experimental evidence also supports this protective effect of lycopene on prostate health.

Soy isoflavones (mentioned earlier in this review) are also known to provide antioxidant protection to the prostate gland, and soy intake is highly correlated with reduced prostate cancer development in epidemiological and experimental studies.

There has also been the suggestion from human intervention trials (placebo-controlled) that vitamin E (60 IU per day) and selenium (200 mcg per day) supplementation provides antioxidant support to the prostate, resulting in a 30-60% reduction in risk of prostate cancer. (35-41,4,11)

What are the ways to Protect The Prostate?

To help combat the age-related changes to the prostate gland that lead to problems of enlargement and the multi-step processes involved in prostate cancer development, all men should practice prudent nutritional practices throughout their lifetime.

Due to the changes that occur at around age 40, men this age and older may consider taking a supplement that contains the correct dosage and standardized grade of saw palmetto, pygeum africanum, beta-sitosterol, soy isoflavones, stinging nettle, lycopene and other prostate-related nutrients as a form of chemoprevention and for general prostate gland support.

The current scientific evidence suggests that the diet and prostate cancer are strongly linked and the following nutrition and lifestyle factors can favourably affect prostate health and should be strongly considered by all men throughout their lifetime:

  1. Consume a diet that is low in saturated fat, trans fats, and deep fried foods.
  2. Remain at or near your ideal body weight.
  3. Consume alcohol in moderation or not at all.
  4. Consume tomato and tomato products on a daily basis.
  5. Use more soy products, such as tofu, veggie burgers, miso soup, soy nuts and soymilk.
  6. By age 40, consider taking a prostate support supplement that contains all the prostate herbal and accessory nutrients reviewed in this report. It is vital that the herbal and accessory compounds are present at the correct dosage and standardized grades, in order to yield sufficient amounts of their bioactive agents to be effective.
  7.  Take a high potency multi vitamin and mineral that is enriched with other antioxidants, including vitamin E succinate (400 IU), selenium (100-200 mcg), vitamin C (1000 mg), etc.
  8. Ingest cruciferous vegetables a minimum of 3-5 times per week.
  9. Remain fit, especially from a cardiovascular fitness standpoint, striving to achieve a resting heart rate of below 60 beats per minute.
  10. Avoid pan-fried meats and other sources of heterocyclic amines (charred BBQ meats and blackened fish and meats).
  11. Drink 4-8 ounces of pomegranate juice daily
  12. Ingest two heaping tablespoons of ground flaxseed daily
  13. Supplement with 1500- 2000 IU of Vitamin D per day (ensuring that your Vitamin D blood level is above 85nmol/L).
  14. Take an essential fatty acid supplement each day, containing borage seed, flaxseed and fish oil (2-3 capsule per day)
  15. Drink 3-5 cups of green tea daily.
  16.  After age 40 take a supplement containing melatonin (1-3 mg one hour before bedtime)

References

  1. Sarma, A.V., Schottenfeld, D. Prostate cancer incidence, mortality, and survival trends in the United States: 1981-2001. Semin Urol Oncol 2002 Feb; 20 (1): 3-9
  2. Willet, W. Estimates of cancer deaths avoidable by dietary change. J Natl Cancer Instit., 1996; 86, 14: 948
  3. Shimizu, H., et al. Cancers of the breast and prostate among Japanese and white immigrants in Los Angeles County. Br J Cancer, 1991; 63: 963-966
  4. Mitchell, J., et al. Effects of phytoestrogens on growth and DNA integrity in human prostate tumor cell lines: PC-3 and LNCaP. Nutr and Cancer, 2000; 38, 2: 223-228
  5. Sesso, H.D., Paffenbarger, R.S. Jr., Lee, I.M. Alcohol consumption and risk of prostate cancer: The Harvard Alumni Health Study. Int J Epidemiol 2001. Aug; 30 (4): 749-55
  6. Bogen, K.T., Keating, G.A. U.S. dietary exposures to heterocyclic amines. J Expo Anal Environ Epidemiol, 2001, May-Jun; 11(3): 155-68
  7. Chinni, S.R., Li, Y., Upadhyay, S., Koppolu, P.K., Sarkar, F.H. Indole-3-carbinol (I3C) induced cell growth inhibition, G1 cell cycle arrest and apoptosis in prostate cancer cells. Oncogene 2001, May 24; 20 (23): 2927-36
  8. Fitzpatrick, A.L., Daling, J.R., Furberg, C.D., Kronmal, R.A., Weissfeld, J.L. Hypertension, heart rate, use of antihypertensives, and ancident prostate cancer. Ann Epidemiol 2001, Nov.; 11 (8): 534-42
  9. Hennenfront, B., et al. American Prostate Society Quarterly, 1995; 3:9
  10. Murray, M. The Healing Power of herbs (2nd edit.) Prima Publishing. 1995: 306-313
  11. Pollard, M., et al. Influence of isoflavones in soy protein isolates on development of induced prostate-related cancers in L-W rats. Nutr and Cancer, 1997; 28, 1: 41-45
  12. Pollard, M., et al. Prevention and treatment of experimental prostate cancer in Lobund-Wister rats: Effects of estradiol, dihydrotestosterone and castration. Prostate, 1989, 15: 95-103
  13. Small, E.J., et al. Prospective trial of the herbal supplement PC-SPES in patients with progressive prostate cancer. J Clinical Oncology, 20000; 18, 21: 3595-3603
  14. Thompson, J.M. et al: Chemoprevention of prostate cancer. Semin Urol 1995;13:122-9
  15. Sultan, C. et al: Inhibition of androgen metabolism and binding by a liposterolic extract of Serenoa repens B in human foreskin fibroblasts. J Steroid Biochem 20, 515-519, 1984
  16. Di Silverio, E. et al: Evidence that Serenoa repens extract displays antiestrogenic activity in prostatic tissue of benign prostatic hypertrophy. Eur Urol 21, 309-314, 1992
  17. Boccafoschi and Annosica, S: Comparison of Serenoa repens extract with placebo by controlled clinical trial in patients with prostatic adenomatosis. Urologia, 50, 1257-1268, 1983.
  18. Mattei, F.M., Capone, M. and Acconcia, A.: Serenoa repens extract in the medical treatment of benign prostatic hypertrophy. Urologia 55, 547-552, 1988
  19. Braeckman, J.: The extract of Serenoa repens in the treatment of benign prostatic hyperplasia: A multi-center open study. Curr Ther Res 55, 776-785, 1984.
  20. Pansadoro, V. and Benincasa, A.: Prostatic hypertrophy: Results obtained with Pygeum africanum extract. Minerva Med 11, 119-144, 1972.
  21. Dufour, B. and Choquenet, C.: Trial controlling the effects of Pygeum africanum extract on the functional symptoms of prostatic adenoma. Ann Urol 18, 193-195, 1984
  22. Menchini-Fabris, G.F., et al: New perspectives of treatment of prostato-vesicular pathologies with Pygeum africanum. Arch Int Urol 60, 313-322, 1988
  23. Wilt T. J. et al:  Beta-sitosterol for the treatment of benign prostatic hyperplasia:  a systematic review. Br J Urol Jun; 83 (a): 976-83, 1999.
  24. Berges R.R. et al:  Treatment of sympotomatic benign prostaic hyperplasia with beta-sitosterol:  an 18 month follow-up.  Br J Urol, May;85 (7): 842-46, 2000.
  25. Dreikorn K. et al:  Status of phyto therapeutic drugs in the treatment of benign prostatic hyperplasia [German] Urologe A.  1995;34(2):119-29.
  26. Buck A.  Phyto therapy for the Prostate.  Br J Urol, 1996;78: 325-336.
  27. Hartmann R. et al.  Inhibition of 5 alpha reductase and aromatase by PHL-00801, a combination of pygeum africanum and urtica dioica extracts.  Phytomedicine, 1996;3 (2): 121-128.
  28. McCaleb R.  Synergistic action of pygeum and nettle root extracts in prostate disease.  Herbalgram, 1996;40:18.
  29. Peterson G. et al.  Genistein and biochanin A.  Inhibit the growth of human prostate cancer cells but not epidermal growth factor receptor auto phosphorylation.  Prostate 1993;22:335-45.
  30. Naik H.R. et al.  An in vitro and in vivo study of anti-tumor effects of genistein on hormone refractory prostate cancer.  Anticancer Res. 1994;14:2617-20.
  31. Kyle E. et al.  Genistein-induced apoptosis of prostate cancer cells is preceded by a specific decrease in focal adhesion kinase activity.  Mol Pharmacol 1997; 51:193-200.
  32. Evans B.A.J. et al.  Inhibition of 5-alpha-reductase in genital skin fibroblasts and prostate tissue by dietary lignans and isoflavonoids.  J. Endocrinology 1995; 147:295-302.
  33. Lu L. et al.  Effects of one-month soya consumption on circulating steroids in men:  Pro. Am. Assoc.  Cancer Research 1996; 37:220 (abstr.).
  34. Messina M.  Legumes and soybeans: an overview of their nutritional profiles and health effects.  AM J Clin Nutr. 1999; 70 (Suppl): 439-50.
  35. Giovanncci et al: Intake of carotenoids and retinol in relation to risk of prostate cancer. J Natl Cancer Inst 1995; 87; 23:1767-76
  36. Heinonen, O.P. et al: Prostate cancer and supplementation with Alpha-Tocopheral and Beta-Carotene: Incidence and mortality in a controlled trial. J Natl Cancer Inst 1998; 90; 6:440-446
  37. Olson, K.B. et al. Vitamins A and E: Further clues for prostate cancer prevention. J Natl Cancer Inst. 1998; 90; 6: 414-415
  38. Linehan, W.M. Inhibition of prostate cancer metastasis: A critical challenge ahead. J Natl Cancer Inst. 1995; 87; 5:331-332
  39. Rao, V.A., et al: Serum and Tissue Lycopene and Biomarkers of Oxidation in Prostate Cancer Patients: A Case-Control Study. Nutrition and Cancer, 1999. 33(2), 159-164.
  40. Gann, P.H., et al. Lower prostate cancer risk in men with elevated lycopene levels: results of a prospective analysis. Cancer Res, 1999; 59, 6: 1225-1230
  41.  Clark, L.C., et al. Effects of selenium supplementation for cancer prevention in patients with carcinoma of the skin. A randomized-controlled trial. Nutritional Prevention of Cancer Study Group. JAMA; 1996, 276 (24): 1957-1963

About the Author

Dr. James Meschino, DC, MS, ROHP, is an educator, author, and researcher having lectured to thousands of healthcare professionals across North America. He holds a Master’s Degree in Science with specialties in human nutrition and biology and is recognized as an expert in the field of nutrition, anti-aging, fitness, and wellness as well as the author of numerous books.

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