Cancer

The carcinogenic process can be modulated, as new treatments unfold. This section presents varied studies, demonstrating the pros and cons of hormone modulation, supplementation, obesity and other lifestyle issues that may be therapeutically exploited. Review current research and medical articles on cancer and its response or relationship to these factors.


Prostate Cancer and the Testosterone ‘Myth’.pdf

In this interview, Abraham Morgentaler, M.D. concludes his comments saying that “testosterone treatment can be enormously helpful for many men. Attitudes are shifting with regard to its relationship to prostate cancer.” He references his article on the subject that appeared in European Urology in 2006.
(2007, February 25). Prostate cancer and the testosterone ‘myth’ [Electronic version]. Vitasearch.com. (PDF).

Mortality Greater for Hip Fracture Than Breast Cancer in Elderly Women.pdf

Older women are at greater risk for death after hip fracture than after breast cancer, according to a presentation at the American Geriatrics Society (AGS) annual meeting held in Seattle, Washington. The investigators suggest that increased awareness of mortality associated with hip fracture is needed to improve preventive measures.
Barclay, L. (2007, May 18). Mortality greater for hip fracture than breast cancer in elderly women [Electronic version]. Medscape Medical News. Retrieved May 31, 2007.

Calcium and Vitamin D Intake and Risk of Colorectal Cancer - The Multiethnic Cohort Study.pdf

The associations of intakes of calcium and vitamin D with colorectal cancer risk were examined in the Multiethnic Cohort Study (Hawaii and Los Angeles, California). In 1993-1996, 85,903 men and 105,108 women aged > or =45 years completed a quantitative food frequency questionnaire. The findings support the hypothesis of protective roles for calcium, vitamin D, and dairy products in the risk of colorectal cancer.
Park, S.Y., Murphy, S.P., Wilkens, L.R., Nomura, A.M., Henderson, B.E. & Kolonel, L.N. (2007). Calcium and vitamin D intake and risk of colorectal cancer - The Multiethnic Cohort Study [Electronic version].  American Journal of Epidemiology, 165(7), 784-793. Retrieved May 14, 2007.

Fiber Crucial to Breast Health in Premenopausal Women.pdf

According to this article, researchers suggest that fiber may support health in premenopausal women because antioxidant nutrients in high-fiber foods have protective properties against reactive oxygen species. Another theory, they suggested, is that fiber may stabilize insulin levels in the body, since hyperglycemia may be a potential cause of cancer. Another theory why fiber may be important to breast health, they suggested, revolves around estrogen’s role in the development of breast cancer.
VRP Staff. (2007). Fiber crucial to breast health in premenopausal women [Electronic version]. Vitamin Research Products Website. Retrieved May 31, 2007.

Combination Hormone Replacement Therapy Linked to Lower-Risk Breast Cancers.pdf

The types of breast tumors that occur after combination hormone replacement therapy in the peri- and post-menopausal period tend to have a better prognosis than those that occur after estrogen-only replacement therapy, Swedish researchers report.
(2006, May 9). Combination hormone replacement therapy linked to lower-risk breast cancers [Electronic version]. Reuters Health. Retrieved May 31, 2007.

Neoadjuvant Mitoxantrone and Docetaxel for High-Risk Localized Prostate Cancer.pdf

This study concluded that administration of multi-agent chemotherapy before prostatectomy was safe in this population. This regimen appeared to have antineoplastic activity as evidenced by PSA reductions in the absence of significant testosterone changes. The benefit of chemotherapy for improving surgical margin rates could not be determined outside of a phase III trial because the effect of patient or surgeon factors could not be dissected from the potential effect of neoadjuvant therapy.
Garzotto, M., Myrthue, A., Higano, C.S. & Beer, T.M. (2006). Neoadjuvant mitoxantrone and docetaxel for high-risk localized prostate cancer [Electronic version]. Urologic Oncology, 24(3), 254-259. Retrieved November 27, 2006.

Does Growth Hormone Cause Cancer?.pdf

This study concluded that even if GH/IGF-1 therapy does result in a small increase in cancer risk compared to untreated patients with GH deficiency, it is likely that the eventual risk will be the same as the general population. Such a restoration to normality will need to be balanced against the known morbidity of untreated GH deficiency.
Jenkins, P.J., Mukherjee, A. & Shalet, S.M. (2006). Does growth hormone cause cancer? [Electronic version]. Clinical Endocrinology (Oxford), 64(2), 115-121. Retrieved November 14, 2006.

Do Differences in Age Specific Androgenic Steroid Hormone Levels Account for Differing Prostate Cancer Rates Between Arabs and Caucasians?.pdf

This study concluded that serum TT, SHBG, DHEAS and ADT levels are significantly lower in Arab men compared to those reported for Caucasian men, especially in early adulthood. Arab men with newly diagnosed prostate cancer have higher circulating androgens compared to healthy controls. We suggest that low circulating androgens and their adrenal precursors in Arab men when compared to Caucasians may partially account for the relatively lower risk for prostate cancer among Arab men.
Kehinde, E.O., Akanji, A.O., Al-Hunayan, A., Memon, A., Luqmani, Y., Al-Awadi, K.A., et al. (2006). Do differences in age specific androgenic steroid hormone levels account for differing prostate cancer rates between Arabs and Caucasians? [Electronic version]. International Journal of Urology, 13(4), 354-361. Retrieved November 27, 2006.

Low Serum Testosterone and Mortality in Male Veterans.pdf

This study used a clinical database to identify men older than 40 years with repeated testosterone levels obtained from October 1, 1994 to December 31, 1999, and without diagnosed prostate cancer. It concluded that low testosterone levels were associated with increased mortality in male veterans. Further prospective studies are needed to examine the association between low testosterone levels and mortality.
Shores, M.M., Matsumoto, A.M., Sloan, K.L. & Kivlahan, D.R. (2006). Low serum testosterone and mortality in male veterans [Electronic version]. Archives of Internal Medicine, 166(15), 1660-1665. Retrieved August 28, 2006.

Combined Estrogen and Testosterone Use and Risk of Breast Cancer in Postmenopausal Women.pdf

According to this study, consistent with the elevation in risk for endogenous testosterone levels, women using estrogen and testosterone therapies have a significantly increased risk of invasive breast cancer.
Tamimi, R.M., Hankinson, S.E., Chen, W.Y., Rosner, B.. & Colditz, G.A. (2006). Combined estrogen and testosterone use and risk of breast cancer in postmenopausal women [Electronic version]. Archives of Internal Medicine, 166(14), 1483-1489. Retrieved November 14, 2006.

Prostate Carcinoma Incidence in Relation to Prediagnostic Circulating Levels of Insulin-Like Growth Factor I, Insulin-Like Growth Factor Binding Protein 3, and Insulin.pdf

In this study, the IGF-1 level was not associated positively with the risk of prostate carcinoma; however, an increase in the IGFBP-3 level was associated with a modest decrease in risk.
Chen, C., Lewis, S.K., Voigt, L., Fitzpatrick, A., Plymate, S.R. & Weiss, N.S. (2005). Prostate carcinoma incidence in relation to prediagnostic circulating levels of insulin-like growth factor I, insulin-like growth factor binding protein 3, and insulin [Electronic version]. Cancer, 103(1), 76-84. Retrieved May 17, 2005.

Vitamin E Supplementation Raised Chances of New Cancer in at-Risk Patients.pdf

Researchers have reported that cancer patients who took high-dose vitamin E supplements to protect themselves from a recurrence of the disease were actually at higher risk of getting a second cancer while taking the supplement than those in a placebo group.
Vitamin E supplementation raised chances of new cancer in at-risk patients. (2005). [Electronic version]. Nutraingredientsusa.com. Retrieved May 17, 2005.

Prostatic Specific Antigen in Patients with Hypogonadism: Effect of Testosterone Replacement.pdf

The current study demonstrated that the level of PSA was not significantly changed after 1 year of testosterone replacement therapy in patients with hypogonadism associated with ED.
El-Sakka, A.I., Hassoba, H.M., Elbakry, A.M. & Hassan, H.A. (2005). Prostatic specific antigen in patients with hypogonadism: effect of testosterone replacement [Electronic version]. The Journal of Sexual Medicine, 2(2), 235-240. Retrieved November 13, 2006.

Obesity, Weight Gain, and Risk of Biochemical Failure Among Prostate Cancer Patients Following Prostatectomy.pdf

The findings of this study validate the importance for a role of obesity in prostate cancer progression and suggest a link to the biological basis of prostate cancer progression that can be therapeutically exploited.
Strom, S.S., Wang, X., Pettaway, C.A., Logothetis, C.J., Yamamura, Y., Do, K, et al. (2005). Obesity, weight gain, and risk of biochemical failure among prostate cancer patients following prostatectomy [Electronic version]. Clinical Cancer Research, 11, 6889-6894. Retrieved October 20, 2005.

Hormone Replacement, the Male Version.pdf

According to this article, a growing number of men in the United States are now taking testosterone to reverse the gradual, age-related decline of the hormone, or so-called andropause. By some estimates, the number of testosterone prescriptions in the United States has tripled in recent years, and total sales now come to about $400 million a year. That’s not much compared with the $12.5 billion spent on cholesterol-lowering statins, but the upward trend is still impressive.
(2004, May). Hormone replacement, the male version [Electronic version]. Harvard Health Letter. Retrieved May 2, 2007.

The Women’s Health Initiative 2004 – Review and Critique.pdf

This article reviews the published results from the Women’s Health Initiative (WHI) and their various interpretations. The WHI was designed to define the risks and benefits of interventions, notably hormone therapy, to potentially prevent heart disease, breast and colorectal cancer, and osteoporotic fractures in postmenopausal women.
Goldman, J.A. (2004). The Women’s Health Initiative 2004 – Review and Critique [Electronic version]. Medscape General Medicine, 6(3). Retrieved September 27, 2005.

Androgen Replacement After Curative Radical Prostatectomy for Prostate Cancer in Hypogonadal Men.pdf

According to this study, based on the clinical experience with this small group of men, and indirect evidence of the safety of this approach from epidemiological and clinical data, further cautious use of testosterone in a carefully selected population seems warranted.
Kaufman, J.M. & Graydon, R.J. (2004). Androgen replacement after curative radical prostatectomy for prostate cancer in hypogonadal men [Electronic version]. The Journal of Urology, 172(3), 920-922. Retrieved November 21, 2005.

Potential Anabolic Effects of Androgens on Bone.pdf

With the decrease of estrogen at menopause, the need for androgens increases in post-menopausal women.  Androgens also appear to be important for the bone health of women who are pre-menopausal.
Kearns, A.E. & Khosla, S. (2004). Potential anabolic effects of androgens on bone [Electronic version]. Mayo Clinic Proceedings, 79(4 Suppl.), S14-18. Retrieved May 18, 2005.

Review of the Book The Sexy Years: Discover the Hormone Connection: The Secret to Fabulous Sex, Great Health, and Vitality, for Women and Men.pdf

Review by Amazon.com of Suzanne Somers’ book The Sexy Years: Discover the Hormone Connection: The Secret to Fabulous Sex, Great Health, and Vitality, for Women and Men.
Lightner, J. (2004). [Review of the book The sexy years: Discover the hormone connection: the secret to fabulous sex, great health, and vitality, for women and men]. Retrieved September 10, 2004.

Risks of Testosterone-Replacement Therapy and Recommendations for Monitoring.pdf

According to this study, hypogonadism affects an estimated 2 million to 4 million men in the United States; its prevalence increases with age. However, it has been estimated that only 5 percent of affected men currently receive treatment. Recent interest in testosterone therapy has been fueled not only by increased medical awareness of the effects of hypogonadism, but also by media attention regarding hormone-replacement therapy in both men and women, the marketing of new topical testosterone formulations, and the desire of "baby boomers" to maintain vigor and health into their more mature years.
Rhoden, E.L. & Morgentaler, A. (2004). Risks of testosterone-replacement therapy and recommendations for monitoring [Electronic version]. The New England Journal of Medicine, 350(5), 482-492. Retrieved September 27, 2005.

Increased Risk of Breast Cancer Following Different Regimens of Hormone Replacement Therapy Frequently Used in Europe.pdf

The aim of this study was to investigate whether different treatment regimens or the androgenecity of progestins influence the risk of breast cancer differently.
Stahlberg, C., Pedersen, A.T., Lynge, E., Andersen, Z.J., Keiding, N., Hundrup, Y.A., et al. (2004). Increased risk of breast cancer following different regimens of hormone replacement therapy frequently used in Europe [Electronic version]. International Journal of Cancer, 109(5), 721-727. Retrieved November 21, 2005.

High Levels of Circulating Testosterone Are Not Associated with Increased Prostate Cancer Risk: A Pooled Prospective Study.pdf

In this study, no support was found for the hypothesis that high levels of circulating androgens within a physiologic range stimulate development and growth of prostate cancer.
Stattin, P., Lumme, S., Tenkanen, L., Alfthan, H., Jellum, E., et al. (2004). High levels of circulating testosterone are not associated with increased prostate cancer risk: a pooled prospective study [Electronic version]. International Journal of Cancer, 108(3), 418-424. Retrieved September 27, 2005.

Growth Hormone Replacement Therapy Appears Safe in Long Term.pdf

Rates of death, cancers, and intracranial tumor growth do not appear to be increased by growth hormone replacement therapy in adults, Mark L. Hartman, M.D., reported at the 12th International Congress of Endocrinology.
Tucker, M.E. (2004). Growth hormone replacement therapy appears safe in long term. Family Practice News, 34(21). Retrieved May 17, 2005.

Effects of Estrogen Plus Progestin on Gynecologic Cancers and Associated Diagnostic Procedures: The Women's Health Initiative Randomized Trial.pdf

This randomized trial suggests that continuous combined estrogen plus progestin therapy may increase the risk of ovarian cancer while producing endometrial cancer rates similar to placebo. The increased burden of endometrial biopsies required to assess vaginal bleeding further limits the acceptability of this regimen. These data provide additional support for caution in the use of continuous combined hormones.
Anderson, G.L., Judd, H.L., Kaunitz, A.M., Barad, D.H., Beresford, S.A., Pettinger, M., et al. (2003).  Effects of estrogen plus progestin on gynecologic cancers and associated diagnostic procedures: The Women's Health Initiative Randomized Trial [Electronic version]. The Journal of the American Medical Association, 290(13), 1739-1748. Retrieved December 7, 2005.

Endogenous Sex Hormones and Prostate Cancer Risk: A Case-Control Study Nested Within the Carotene and Retinol Efficacy Trial.pdf

In this study, the inverse association between E2 and prostate cancer risk was largely restricted to men with blood collection within 3 years of diagnosis. The results add to the evidence that serum testosterone is unrelated to prostate cancer incidence. The suggestions that intraprostatic androgen activity may increase risk and that serum estrogens may decrease risk, warrant additional study.
Chen, C., Weiss, N.S., Stanczyk, F.Z., Lewis, S.K., DiTommaso, D., et al. (2003). Endogenous sex hormones and prostate cancer risk: a case-control study nested within the Carotene and Retinol Efficacy Trial [Electronic version]. Cancer Epidemiology, Biomarkers & Prevention: A Publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 12(12), 1410-1416. Retrieved September 27, 2005.

Influence of Estrogen Plus Progestin on Breast Cancer and Mammography in Healthy Postmenopausal Women: The Women's Health Initiative Randomized Trial.pdf

This study concluded that relatively short-term combined estrogen plus progestin use increases incident breast cancers, which are diagnosed at a more advanced stage compared with placebo use, and also substantially increases the percentage of women with abnormal mammograms. These results suggest estrogen plus progestin may stimulate breast cancer growth and hinder breast cancer diagnosis.
Chlebowski, R.T., Hendrix, S.L., Langer, R.D., Stefanick, M.L., Gass, M., Lane, D., et al. (2003). Influence of estrogen plus progestin on breast cancer and mammography in healthy postmenopausal women: The Women's Health Initiative Randomized Trial [Electronic version]. The Journal of the American Medical Association, 289(24), 3243-3253. Retrieved December 7, 2005.

Insulin Resistance and Prostate Cancer Risk.pdf

In this study, the associations between prostate cancer risk and insulin sensitivity or resistance were independent of total caloric intake and serum levels of insulin-like growth factors, sex hormones, and sex hormone-binding globulin. Because of the retrospective design of this study, the role of insulin resistance in prostate cancer needs to be confirmed in prospective studies.
Hsing, A.W., Gao, Y.T., Chua, S., Jr., Deng, J. & Stanczyk, F.Z. (2003). Insulin resistance and prostate cancer risk [Electronic version]. Journal of the National Cancer Institute, 95(1), 67-71. Retrieved September 27, 2005.

Growth Hormone Protects Human Lymphocytes from Irradiation-Induced Cell Death.pdf

According to this study, undesired effects of cancer radiotherapy mainly affect the hematopoietic system. Growth hormone (GH) participates in both hematopoiesis and modulation of the immune response.
Lempereur, L., Brambilla, D., Scoto, G.M., D'Alcamo, M., Goffin, V., Crosta, L., et al. (2003). Growth hormone protects human lymphocytes from irradiation-induced cell death [Electronic version]. British Journal of Pharmacology, 138(8), 1411-1416. Retrieved December 7, 2005.

Pretreatment Total Testosterone Level Predicts Pathological Stage in Patients with Localized Prostate Cancer Treated with Radical Prostatectomy.pdf

This study concludes that pretreatment total testosterone was an independent predictor of extraprostatic disease in patients with localized prostate cancer. As testosterone decreases patients have an increased likelihood of non-organ confined disease. Low testosterone was not predictive of biochemical recurrence, although trends observed dictate study in larger cohorts with mature followup.
Massengill, J.C., Sun, L., Moul, J.W., Wu, H., McLeod, D.G., et al. (2003). Pretreatment total testosterone level predicts pathological stage in patients with localized prostate cancer treated with radical prostatectomy [Electronic version]. The Journal of Urology, 169(5), 1670-1675. Retrieved September 27, 2005.

Testosterone Replacement Therapy in Hypogonadal Men at High Risk for Prostate Cancer: Results of 1 year of Treatment in Men with Prostatic Intraepithelial Neoplasia.pdf

This study concludes that after 1 year of testosterone replacement therapy (TRT) men with prostatic intraepithelial neoplasia (PIN) do not have a greater increase in PSA or a significantly increased risk of cancer than men without PIN. These results indicate that TRT is not contraindicated in men with a history of PIN.
Rhoden, E.L. & Morgentaler, A. (2003). Testosterone replacement therapy in hypogonadal men at high risk for prostate cancer: Results of 1 year of treatment in men with prostatic intraepithelial neoplasia. The Journal of Urology, 170(6, Part 1 of 2), 2348-2351. Retrieved September 27, 2005.

Prostate Cancer and Prostate-Specific Antigen: The More We Know, the Less We Understand.pdf

This editorial discusses PSA and in particular the Cramer et al study that observes that PSA values may be related to polymorphisms in the PSA gene promoter.
Thompson, I., Leach, R.J., Pollock, B.H. & Naylor, S.L. (2003). Prostate cancer and prostate-specific antigen: the more we know, the less we understand [Electronic version]. Journal of the National Cancer Institute, 95(14), 1027-1028. Retrieved January 4, 2006.

Overweight, Obesity, and Cancer Risk.pdf

According to this article, in addition to an increase in the risk of cardiovascular disease and type II diabetes, the evidence summarized here shows that excess body weight is directly associated with risk of cancer at several organ sites, including colon, breast (in postmenopausal women), endometrium, oesophagus, and kidney.
Bianchini, F., Kaaks, R. & Vainio, H. (2002). Overweight, obesity, and cancer risk [Electronic version]. The Lancet Oncology, 3(9), 565-574. Retrieved January 4, 2006.

Outcomes of Growth Hormone Replacement Therapy in Survivors of Childhood Acute Lymphoblastic Leukemia.pdf

This study suggests that GH replacement therapy is safe and efficacious for the correction of GH deficiency in survivors of childhood acute lymphoblastic leukemia (ALL).
Leung, W., Rose, S.R., Zhou, Y., Hancock, M.L., Burstein, S., et al. (2002). Outcomes of growth hormone replacement therapy in survivors of childhood acute lymphoblastic leukemia [Electronic version]. Clinical Oncology, 20(13), 2959-2964. Retrieved September 26, 2005.

Bone Loss Following Hypogonadism in Men with Prostate Cancer Treated with GnRH Analogs.pdf

These findings of this study demonstrate a significant loss of bone in men with prostate cancer after receiving GnRH therapy and suggest that the total hip and radius are the preferred sites for monitoring bone loss in older men. In addition, markers of bone resorption may be helpful. 
Mittan, D., Lee, S., Miller, E., Perez, R.C., Basler, J.W. & Bruder, J.M. (2002). Bone loss following hypogonadism in men with prostate cancer treated with GnRH analogs [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 87(8), 3656-3661. Retrieved December 7, 2005.
GH-Deficient Survivors of Childhood Cancer: GH Replacement During Adult Life.pdf

This article proposes that, as in patients with hypopituitarism caused by pituitary disease, the main indication for GH replacement in GH-deficient survivors of childhood cancer should be severe impairment of quality of life.
Murray, R.D., Darzy, K.H., Gleeson, H.K. & Shalet, S.M. (2002). GH-deficient survivors of childhood cancer: GH replacement during adult life [Electronic version]. The Journal of Clinical Endocrinology & Metabolism, 87(1), 129-135. Retrieved September 26, 2005.

Risk of Disease Recurrence and Second Neoplasms in Survivors of Childhood Cancer Treated with Growth Hormone: A Report from the Childhood Cancer Survivor Study.pdf

This study concludes that GH therapy does not appear to increase the risk of disease recurrence or death in survivors of childhood cancer. The increased number of SN, particularly in survivors of acute leukemia, is of concern, but the data need to be interpreted with caution given the small number of events.
Sklar, C.A., Mertens, A.C., Mitby, P., Occhiogrosso, G., Qin, J., et al. (2002). Risk of disease recurrence and second neoplasms in survivors of childhood cancer treated with growth hormone: a report from the Childhood Cancer Survivor Study [Electronic version]. The Journal of Clinical Endocrinology & Metabolism, 87(7), 3136-3141. Retrieved September 26, 2005.

Changes in Body Composition During Androgen Deprivation Therapy for Prostate Cancer.pdf

The aim of this study was to determine the effects of initial treatment with a GnRH agonist on body composition in asymptomatic men with nonmetastatic prostate cancer. 
Smith, M.R., Finkelstein, J.S., McGovern, F.J., Zietman, A.L., Fallon, M.A., Schoenfeld, D.A., et al. (2002). Changes in body composition during androgen deprivation therapy for prostate cancer [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 87(2), 599-603. Retrieved December 7, 2005.

Growth Hormone Treatment and Neoplasia-Coincidence or Consequence?.pdf

This special editorial by the Lawson Wilkins Pediatric Endocrine Society (LWPES) Writing Committee discusses the article by Swerdlow et al in Lancet, which reports on the risk of cancer in patients treated with human pituitary GH in the United Kingdom from 1959 to 1985.
Sperling, M.A., Saenger, P.H., Hintz, R., Wilson, T. & Rose, S.R. on behalf of the LWPES Executive Committee and the LWPES Drug and Therapeutics Committee. (2002). Growth hormone treatment and neoplasia-coincidence or consequence? [Electronic version]. The Journal of Clinical Endocrinology & Metabolism, 87(12), 5351-5352. Retrieved September 26, 2005.

Risk of Cancer in Patients Treated with Human Pituitary Growth Hormone in the UK, 1959-85: A Cohort Study.pdf

The interpretation of this study is that although based on small numbers, the risk of colorectal cancer is of some concern and further investigation in other cohorts is needed.  They have no evidence as to whether growth hormone in modern dosage regimens is associated with an increased risk of colorectal cancer.
Swerdlow, A.J., Higgins, C.D., Adlard, P. & Preece, M.A. (2002). Risk of cancer in patients treated with human pituitary growth hormone in the UK, 1959-85: a cohort study [Electronic version]. Lancet, 360(9329), 273-277. Retrieved September 26, 2005.

Association Between Prostate Cancer and Serum Testosterone Levels.pdf

The findings of this study show that serum total and free testosterone levels in patients with prostate cancer are altered, supporting the possibility that prostate cancer may inhibit serum testosterone levels.
Zhang, P.L., Rosen, S., Veeramachaneni, R., Kao, J., DeWolf, W.C., et al. (2002). Association between prostate cancer and serum testosterone levels [Electronic version]. The Prostate, 53(3), 179-182. Retrieved September 27, 2005.

Prostate Cancer Risk and Serum Levels of Insulin and Leptin: A Population-Based Study.pdf

The results of this study suggest that serum insulin levels may influence the risk of prostate cancer in Chinese men. Further research, especially prospective studies, is needed to confirm these findings in high-risk populations and to clarify the underlying mechanisms involved.
Hsing, A.W., Chua, S., Jr., Gao, Y.T., Gentzschein, E., Chang, L., et al. (2001). Prostate cancer risk and serum levels of insulin and leptin: a population-based study [Electronic version]. Journal of the National Cancer Institute, 93(10), 783-789. Retrieved September 27, 2005.

Clinical Perspective - Acromegaly and Cancer: Not a Problem?.pdf

This study discusses how uncontrolled acromegaly may provide a growth advantage to concurrently occurring neoplasms in these patients; and based upon experimental information, cancer in a patient with acromegaly and uncontrolled GH levels will likely be more aggressive, with potentially increased cancer-associated morbidity and mortality. However, there is no clear evidence for enhanced de novo cancer initiation in acromegaly and, as yet, no direct proven causal relationship of acromegaly with malignant disease.
Melmed, S. (2001). Clinical perspective - Acromegaly and cancer: not a problem? [Electronic version]. The Journal of Clinical Endocrinology & Metabolism, 86(7), 2929-2934. Retrieved September 26, 2005.

Low Serum Insulin-Like Growth Factor 1 (IGF-1): A Significant Association with Prostate Cancer.pdf

According to this study, insulin-like growth factor 1 (IGF-1) is an important mitogenic and antiapoptotic peptide that affects the proliferation of normal and malignant cells. Findings of this study indicate a significant association between low serum levels of IGF-1 and prostate cancer.
Baffa, R., Reiss, K., El-Gabry, E.A., Sedor, J., Moy, M.L., Shupp-Byrne, D., et al. (2000). Low serum insulin-like growth factor 1 (IGF-1): a significant association with prostate cancer [Electronic version]. Techniques in Urology, 6(3), 236-239. Retrieved January 3, 2006.

Insulin-Like Growth Factor I is Not a Useful Marker of Prostate Cancer in Men with Elevated Levels of Prostate-Specific Antigen.pdf

According to this study, in screen-positive men with elevated serum PSA, serum IGF-I is not a useful diagnostic test for prostate cancer, but it may be associated with benign prostatic hyperplasia and enlargement.
Finne, P., Auvinen, A., Koistinen, H., Zhang, W.M., Maattanen, L., Rannikko, S., et al. (2000). Insulin-like growth factor I is not a useful marker of prostate cancer in men with elevated levels of prostate-specific antigen [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 85(8), 2744-2747. Retrieved January 3, 2006.

The Significance of Serum Levels of Insulin-Like Growth Factor-1 in Patients with Prostate Cancer.pdf

This study concluded that there was no significant association between IGF-1 serum levels and prostate cancer. Short-term androgen withdrawal using LHRH analogues combined with anti-androgens had no effect on the levels of IGF-1.
Kurek, R., Tunn, U.W., Eckart, O., Aumuller, G., Wong, J. & Renneberg, H. (2000). The significance of serum levels of insulin-like growth factor-1 in patients with prostate cancer [Electronic version]. BJU International, 85(1), 125-129. Retrieved January 3, 2006.

The Prevalence and Characteristics of Colorectal Neoplasia in Acromegaly.pdf

In this study, no associations were found between the presence of colonic neoplasia and the duration of disease, total GH exposure, cure status, and serum insulin-like growth factor I. This study has failed to demonstrate an increased prevalence of neoplasia in acromegalic patients compared with the expected prevalence in the general population and questions the need for an aggressive colonoscopic screening policy.
Renehan, A.G., Bhaskar, P., Painter, J.E., O’Dwyer, S.T., Haboubi, N., et al. (2000). The prevalence and characteristics of colorectal neoplasia in acromegaly [Electronic version]. The Journal of Clinical Endocrinology & Metabolism, 85(9), 3417-3424. Retrieved September 26, 2005.

Effect of Hormone Replacement Therapy on Breast Cancer Risk: Estrogen Versus Estrogen Plus Progestin.pdf

This study provides strong evidence that the addition of a progestin to HRT enhances markedly the risk of breast cancer relative to estrogen use alone. These findings have important implications for the risk-benefit equation for HRT in women using CHRT.
Ross, R.K., Paganini-Hill, A., Wan, P.C. & Pike, M.C. (2000). Effect of hormone replacement therapy on breast cancer risk: estrogen versus estrogen plus progestin [Electronic version]. Journal of the National Cancer Institute, 92(4), 328-332. Retrieved October 3, 2005.

Gender Difference in Insulin-Like Growth Factor I Response to Growth Hormone (GH) Treatment in GH-Deficient Adults:  Role of Sex Hormone Replacement.pdf

The present study confirms short-term data published in the literature on a sex difference in rhGH dose requirement in GH-deficient patients. It furthers extends the data by demonstrating that this sex difference in GH responsivity persists and changes during the 24 months of the study. Moreover, it shows that estrogen replacement blunts the IGF-I response to rhGH in women, whereas in men with androgen substitution the responsivity increases over time, thus bearing a risk of undertreatment in women and overtreatment in men.
Span, J.P., Pieters, G.F., Sweep, C.G., Hermus, A.R. & Smals, A.G. (2000). Gender difference in insulin-like growth factor I response to growth hormone (GH) treatment in GH-deficient adults:  role of sex hormone replacement [Electronic version].  The Journal of Clinical Endocrinology & Metabolism, 85(3), 1121-1125. Retrieved September 26, 2005.

Testosterone: Its Role in Development of Prostate Cancer and Potential Risk from Use as Hormone Replacement Therapy.pdf

According to this article, two observations support the view that the prostate cancer risks from use of testosterone hormone replacement may not be as great as first feared. Firstly, prostate cancers arising in men with low serum testosterone levels are more malignant and frequently nonresponsive to hormones. Secondly, breast cancers diagnosed in women on HRT though increased in number are less malignant possibly because of enhanced sensitivity to hormone therapy, and the situation may prove to be analogous with prostate cancer and testosterone replacement.
Slater, S. & Oliver, R.T. (2000). Testosterone: its role in development of prostate cancer and potential risk from use as hormone replacement therapy [Electronic version]. Drugs & Aging, 17(6), 431-439. Retrieved October 3, 2005.

Long-Term Risk of Gastrointestinal Tumor Recurrence After Postoperative Treatment with Recombinant Human Growth Hormone.pdf

According to this study, the results demonstrate no evidence for an increased risk of tumor recurrence after rhGH treatment for a short period of time after removal of a gastrointestinal adenocarcinoma. Therefore, the positive metabolic effects of rhGH application can be used safely in the treatment of the postoperative catabolic state in the patient groups investigated.
Tacke, J., Bolder, U., Herrmann, A., Berger, G. & Jauch, K.W. (2000). Long-term risk of gastrointestinal tumor recurrence after postoperative treatment with recombinant human growth hormone [Electronic version]. Journal of Parenteral and Enteral Nutrition, 24(3), 140-144. Retrieved January 4, 2006.


Role of the Insulin-Like Growth Factor Family in Cancer Development and Progression.pdf

According to this study, the insulin-like growth factors (IGFs) are mitogens that play a pivotal role in regulating cell proliferation, differentiation, and apoptosis. The effects of IGFs are mediated through the IGF-I receptor, which is also involved in cell transformation induced by tumor virus proteins and oncogene products.
Yu, H. & Rohan, T. (2000). Role of the insulin-like growth factor family in cancer development and progression [Electronic version]. Journal of the National Cancer Institute, 92(18), 1472-1489. Retrieved September 26, 2005.

Growth Hormone, Alone and in Combination with Insulin, Increases Whole Body and Skeletal Muscle Protein Kinetics in Cancer Patients After Surgery.pdf

The aim of this study was to investigate the impact of growth hormone, alone and in combination with insulin, on the protein kinetics of patients with upper gastrointestinal (GI) tract cancer who have undergone surgery and are receiving total parenteral nutrition (TPN). It concluded that growth hormone and GH plus insulin regimens improve protein kinetic parameters in patients with upper GI tract cancer who are receiving TPN after undergoing surgery.
Berman, R.S., Harrison, L.E., Pearlstone, D.B., Burt, M. & Brennan, M.F. (1999). Growth hormone, alone and in combination with insulin, increases whole body and skeletal muscle protein kinetics in cancer patients after surgery [Electronic version]. Annals of Surgery, 229(1), 1-10. Retrieved January 4, 2006.

Lower Prostate Cancer Risk in Men with Elevated Plasma Lycopene Levels: Results of a Prospective Analysis.pdf

According to this study, for men with low lycopene, beta-carotene supplements were associated with risk reductions comparable to those observed with high lycopene. These data provide further evidence that increased consumption of tomato products and other lycopene-containing foods might reduce the occurrence or progression of prostate cancer.
Gann, P.H., Ma, J., Giovannucci, E., Willett, W., Sacks, F.M., et al. (1999). Lower prostate cancer risk in men with elevated plasma lycopene levels: results of a prospective analysis [Electronic version]. Cancer Research, 59(6), 1225-1230. Retrieved September 27, 2005.

Hormone Replacement Therapy and Breast Cancer Risk in a Nationally Representative Cohort.pdf

This study, based on a nationally representative cohort followed for up to 22 years, failed to find an increased risk of breast cancer associated with the use of HRT. It provides further evidence that if there is an increased risk of breast cancer associated with HRT use, this risk is small.
Lando, J.F., Heck, K.E. & Brett, K.M. (1999). Hormone replacement therapy and breast cancer risk in a nationally representative cohort [Electronic version]. American Journal of Preventative Medicine, 17(3), 176-180. Retrieved October 3, 2005.

Prospective Study of Colorectal Cancer Risk in Men and Plasma Levels of Insulin-Like Growth Factor (IGF)-I and IGF-Binding Protein-3.pdf

The findings of this study suggest that circulating IGF-I and IGFBP-3 are related to future risk of colorectal cancer.
Ma, J., Pollak, M.N., Giovannucci, E., Chan, J.M., Tao, Y., et al. (1999). Prospective study of colorectal cancer risk in men and plasma levels of insulin-like growth factor (IGF)-I and IGF-binding protein-3 [ Electronic version]. Journal of the National Cancer Institute, 91(7), 620-625. Retrieved September 26, 2005.

Hormone Replacement Therapy and the Risk of Colorectal Cancer: A Meta-Analysis.pdf

This article concludes that the risk of colon cancer may be decreased among recent postmenopausal HRT users. Although data are limited, the risk of fatal colon cancer also may be lower in HRT users.
Nanda, K., Bastian, L.A., Hasselblad, V. & Simel, D.L. (1999). Hormone replacement therapy and the risk of colorectal cancer: a meta-analysis [Electronic version]. Obstetrics and Gynecology, 93(5 Pt. 2), 880-888. Retrieved October 3, 2005.

Hormone Replacement Therapy and Risk of Colon and Rectal Cancer.pdf

This study, one of the largest case-control investigations on exogenous female hormones and colorectal cancer thus far, provides further evidence that women who have ever used HRT are at lower risk of colon and rectal cancer. Because colorectal cancer is the second most common neoplasm and cause of death among nonsmoking women in developed countries, these results may have a major public health impact.
Fernandez, E., La Vecchia, C., Braga, C., Talamini, R., Negri, E., Parazzini, F., et al. (1998). Hormone replacement therapy and risk of colon and rectal cancer [Electronic version]. Cancer Epidemiology, Biomarkers & Prevention, 7(4), 329-333. Retrieved October 3, 2005.

Inhibition of Aberrant Proliferation and Induction of Apoptosis in Pre-Neoplastic Human Mammary Epithelial Cells by Natural Phytochemicals.pdf

In long-term (21 day) experiments, BP treatment induced a 145.3% increase (P=0.001) in anchorage-dependent colony formation. This aberrant proliferation was inhibited by 44.2% to 65.3% (P=0.01) in the presence of the three phytochemicals. Thus, BP-induced aberrant proliferation is inhibited by the natural phytochemicals in part due to regulation of cell cycle progression and induction of p53 dependent apoptosis.
Katdare, M., Osborne, M.P. & Telang, N.T. (1998). Inhibition of aberrant proliferation and induction of apoptosis in pre-neoplastic human mammary epithelial cells by natural phytochemicals [Electronic version]. Oncology Reports, 5(2), 311-315. Retrieved September 27, 2005.

Breast Cancer and Hormone Replacement Therapy: Collaborative Reanalysis of Data from 51 Epidemiological Studies of 52,705 Women with Breast Cancer and 108,411 Women without Breast Cancer. Collaborative Group on Hormonal Factors in Breast Cancer.pdf

The interpretation of this study was that the risk of having breast cancer diagnosed is increased in women using HRT and increases with increasing duration of use. This effect is reduced after cessation of use of HRT and has largely, if not wholly, disappeared after about 5 years. These findings should be considered in the context of the benefits and other risks associated with the use of HRT.
(1997). Breast cancer and hormone replacement therapy: collaborative reanalysis of data from 51 epidemiological studies of 52,705 women with breast cancer and 108,411 women without breast cancer. Collaborative Group on Hormonal Factors in Breast Cancer [Electronic version]. Lancet, 350(9084), 1047-1059. Retrieved October 3, 2005.

The Role of Hormone Replacement Therapy in the Risk for Breast Cancer and Total Mortality in Women with a Family History of Breast Cancer.pdf

The data in this study suggest that HRT use in women with a family history of breast cancer is not associated with a significantly increased incidence of breast cancer but is associated with a significantly reduced total mortality rate.
Sellers, T.A., Mink, P.J., Cerhan, J.R., Zheng, W., Anderson, K.E., Kushi, L,H., et al. (1997). The role of hormone replacement therapy in the risk for breast cancer and total mortality in women with a family history of breast cancer [Electronic version]. Annals of Internal Medicine, 127(11), 973-980. Retrieved October 3, 2005.

Inhibition of Proliferation and Modulation of Estradiol Metabolism: Novel Mechanisms for Breast Cancer Prevention by the Phytochemical Indole-3-Carbinol.pdf

This study says that the preventive efficacy of I3C on human mammary carcinogenesis may be due in part to its ability to regulate cell-cycle progression, increase the formation of antiproliferative E2 metabolite, and induce cellular apoptosis.
Telang, N.T., Katdare, M., Bradlow, H.L., Osborne, M.P. & Fishman, J. (1997). Inhibition of proliferation and modulation of estradiol metabolism: novel mechanisms for breast cancer prevention by the phytochemical indole-3-carbinol [Electronic version]. Proceedings of the Society for Experimental Biology and Medicine, 216(2), 246-252. Retrieved January 19, 2006.

Hormone Replacement Therapy and Endometrial Cancer Risk: A Meta-Analysis.pdf

This study concluded that endometrial cancer risk increases substantially with long duration of unopposed estrogen use, and this increased risk persists for several years after discontinuation of estrogen. Although not statistically significant, the risk of death from endometrial cancer among unopposed estrogen users is increased, similar to the increased risk of developing the disease. Data regarding risk for endometrial cancer among estrogen plus progestin users are limited and conflicting.
Grady, D., Gebretsadik, T., Kerlikowske, K., Ernster, V., & Petitti, D. (1995). Hormone replacement therapy and endometrial cancer risk: a meta-analysis [Electronic version]. Obstetrics and Gynecology, 85(2), 304-313. Retrieved October 3, 2005.

Evidence of a Healthy Estrogen User Survivor Effect.pdf

This article examined the relation between menopausal estrogen use and all-cause and cause-specific mortality in a cohort of over 49,000 women followed between 1979 and 1989 in the Breast Cancer Detection Demonstration Project (BCDDP) Follow-Up Study,

Sturgeon, S.R., Schairer, C., Brinton, L.A., Pearson, T., & Hoover, R.N. (1995). Evidence of a healthy estrogen user survivor effect [Electronic version]. Epidemiology, 6(3), 227-231. Retrieved October 3, 2005.