- We strive to provide complete care for our patients. Learn more about all the services we provide.
You are using an outdated browser. Please upgrade your browser to improve your experience.
Diet and Prostate Cancer
By Larry E. Masula, DC and James P. Meschino, DC, MS
Recent Trends and Research Findings
Prostate cancer incidence increased steadily from 1981 to 1989, with a steep increase in the early 1990s, followed by a decline. However, the exaggerated rate of increase in the early 1990s was transient, likely a result of increased early detection of preclinical prostate cancer from the widespread implementation of the new PSA (prostate-specific antigen) blood-screening test. Nevertheless, prostate cancer remains the most common form of 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 many as 75 percent of prostate cancer cases may be prevented if men follow more prudent nutritional practices, many of which will be outlined in this review.2 In Japan, the incidence of prostate cancer is 80 percent lower than in North America and much of the Western world. Low rates are also found in Africa and
In recent years, a number of nutritional factors and bioactive compounds have been identified that are strongly linked to the development of prostate cancer. In the past year, published data from the Harvard alumni study revealed that men with moderate liquor consumption (three drinks per week to three drinks per day) show a 61-67 percent increased risk of developing prostate cancer, compared to men who never or infrequently consume alcohol. Wine and beer did not appear to be as hazardous as liquor. However, men initiating alcohol consumption of any kind between 1977 to 1988 had double the 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 7,612 Harvard alumni (mean age was 66.6 years) from 1988 -1993.5
Also in 2001, the study by K.T. Bogen and G.A. Keating provided evidence that higher intakes of heterocyclic amines among African-Americans, especially from pan-fried meats, may partially explain the twofold increase in prostate cancer in this group, as it was shown to consume approximately two and three times 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). The authors concluded 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
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, may overstimulate the androgen activity of prostate cells. Increased an-drogen 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 from a cardiovascular health study (2,442 men) demonstrated that men with a resting heart rate equal to or greater than 80 beats per minute had a 60-percent 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 Thus one can draw a strong argument for the inclusion of chiropractic care to help stabilize the sympathetic nervous system output.
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, and 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 percent of men by ages 40-59, and 80 percent 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 important 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 nutrition in lifelong prostate health.
Age-Related Changes to the 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. 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 lifetimes. There is no question that DHT is linked to prostate cancer and prostate enlargement in a number of ways.11,12 Encouraging 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 and (more recently) treatment of prostate cancer.13
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 agents 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 percent 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 (standardized grade containing 90 percent fatty acids and sterols) or 320 mg (twice daily) of a standardized grade containing 45 percent 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 (standardized grade containing12-14 percent 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 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, including soy extract, are several important isoflavones, the most important being genistein and diadzein. These isoflavones directly inhibit the build-up of DHT and exhibit many other biological properties related to the prevention of prostate disease and prostate enlargement as men age. Soy isoflavones have been shown to induce apoptosis 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. In
The herb stinging nettle 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
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 and intake levels (six mg per day), and a marked reduction in prostate cancer development (as much as a 40-percent 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. 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 provide antioxidant support to the prostate, resulting in a 30 to 60 percent reduction in the risk of prostate cancer.4,11,35-41
Protecting the Prostate
To help combat the age-related changes to the prostate gland that lead to problems of enlargement, and the multistep processes involved in prostate cancer development, all men should practice prudent nutritional practices. Due to the changes that occur at around age 40, men this age and older should 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 general prostate gland support. The scientific evidence suggests that the following nutrition and lifestyle factors can favourably affect prostate health, and should be strongly considered by all men:
1. Consume a diet that is low in saturated fat.
2. Remain at or near your ideal body weight.
3. Consume alcohol in moderation, or not at all.
4. Consume tomatoes and tomato products daily.
5. Use more soy products: 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 dosages and standardized grades to yield sufficient amounts of their bioactive agents.
7. Consider taking a high-potency multivitamin and mineral supplement that is enriched with other antioxidants, including vitamin E
(400 IU), selenium (100-200 mcg), vitamin C (1,000 mg), etc.
8. Eat cruciferous vegetables a minimum of three to five times per week.
9. Remain fit, especially from a cardiovascular fitness standpoint, striving to achieve a resting heart rate of below 60 beats per
10. Avoid pan-fried meats and other sources of heterocyclic amines (charred BBQ meats and blackened fish and meats).
1. Sarma AV, Schottenfeld D. Prostate cancer incidence, mortality, and survival trends in the
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
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 HD, Paffenbarger RS Jr., Lee IM. Alcohol consumption and risk of prostate cancer. The Harvard Alumni Health Study. Int J Epidemiol 2001Aug;30(4):749-55.
6. Bogen KT,
7. Chinni SR, Li Y, Upadhyay S, Koppolu PK, Sarkar FH. 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 AL, Daling JR, Furberg CD, Kronmal RA, Weissfeld JL. Hypertension, heart rate, use of antihypertensives, and incident prostate cancer. Ann Epidemiol 2001, Nov;11(8):534-42.
9. Hennenfront B, et al. American Prostate Society Quarterly 1995;3:9.
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 EJ, et al. Prospective trial of the herbal supplement PC-SPES in patients with progressive prostate cancer. J Clinical Oncology 2000;18(21):3595-3603.
14. Thompson JM, 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 1984;20:515-519.
16. Di Silverio E, et al. Evidence that Serenoa repens extract displays antiestrogenic activity in prostatic tissue of benign prostatic hypertrophy. Eur Urol 1992;21:309-314.
17. Boccafoschi and Annosica S. Comparison of Serenoa repens extract with placebo by controlled clinical trial in patients with prostatic adenomatosis. Urologia 1983;50:1257-1268, 1983.
18. Mattei FM, Capone M, Acconcia, A. Serenoa repens extract in the medical treatment of benign prostatic hypertrophy. Urologia 1988;55:547-552.
19. Braeckman J. The extract of Serenoa repens in the treatment of benign prostatic hyperplasia. A multi-center open study. Curr Ther Res 1994;55:776-785.
20. Pansadoro V, Benincasa A. Prostatic hypertrophy: Results obtained with pygeum africanum extract. Minerva Med 1972;11:119-144.
21. Dufour B, Choquenet C. Trial controlling the effects of pygeum africanum extract on the functional symptoms of prostatic adenoma. Ann Urol 1984;18:193-195.
22. Menchini-Fabris GF, et al. New perspectives of treatment of prostato-vesicular pathologies with pygeum africanum.
Arch Int Urol 1988;60:313-322.
23. Wilt TJ, et al. Beta-sitosterol for the treatment of benign prostatic hyperplasia: a systematic review. Br J Urol Jun 1999;83(a):976-83.
24. Berges RR, et al. Treatment of sympotomatic benign prostaic hyperplasia with beta-sitosterol: an 18-month follow-up. Br J Urol, May 2000;85(7):842-46.
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. Phytotherapy 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 HR, 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 BAJ, 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).
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 OP, 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 KB, et al. Vitamins A and E: Further clues for prostate cancer prevention. J Natl Cancer Inst 1998;90;6: 414-415.
38. Linehan WM. Inhibition of prostate cancer metastasis: A critical challenge ahead. J Natl Cancer Inst 1995;87;5:331-332.
40. Gann PH, 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 LC, 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.
Sign-up using the form or call us at 530-342-6441 to learn more about us.
|Monday||8:30am - 12pm||2pm-6:00pm|
|Tuesday||8:30am - 12pm||2pm - 5:00pm|
|Wednesday||8:30am - 12pm||2pm - 6:00pm|
|Thursday||8:30am - 12pm||2pm - 6:00pm|
|Friday||8:30am - 12pm||2pm - 5:00pm|
|8:30am - 12pm||8:30am - 12pm||8:30am - 12pm||8:30am - 12pm||8:30am - 12pm||Closed||Closed|
|2pm-6:00pm||2pm - 5:00pm||2pm - 6:00pm||2pm - 6:00pm||2pm - 5:00pm||Closed||Closed|
3D Spine Simulator