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Multi-nutrient supplement improves hormone ratio associated with cancer risk
Journal of Translational Medicine volume 11, Article number: 252 (2013)
Gynecological cancers are among the most common in women and are directly related to a variety of hormonal factors. One potential risk factor associated with developing a gynecological malignancy is the ratio of two hormone metabolites, 2-Hydroxyestrone (2-HE) and 16alpha-Hydroxyestrone (16alpha-HE). A number of botanical constituents such as indoles, flavonoids, and resveratrol have been shown to have a favorable effect on the metabolic pathways that affect this ratio. The present study was designed to evaluate if a multi-nutrient supplement containing targeted botanical constituents would affect the 2-HE/16 alpha-HE ratio in middle-aged women.
A retrospective analysis was performed on 76 female patients (mean age 54 years) who received 2-HE/16 alpha-HE ratio assessments at two separate time points. The ratio assessment was part of standard care for women who presented with risk indicators associated with a high proliferative state. All patients who completed pre and post assessments were included. Sixty-five of the patients received a multi-nutrient supplement, Lucentia Peak®, during the study period. Eleven patients chose not to take the supplement, but did receive ratio assessments at similar time points as the treatment group, allowing for between group comparisons. Paired t-tests were used to compare the changes in the 2-HE and 16alpha-HE measures as well as their ratio, both within groups and between groups.
The results demonstrated a significant increase in the 2-HE/16alpha-HE ratio in the treated group (pre 0.38 to post 0.57, p<0.0001), and was significantly different (p=0.02) compared to the change in the control group (pre 0.65 to post 0.64). This change appears to be mediated primarily by an increase in the 2-HE level. Individually, 54 patients given Lucentia Peak® had increased ratios while 11 patients had a decrease. In the control group, 3 patients had an increase in their ratio and 8 patients had a decrease.
The results demonstrated that women receiving the Lucentia Peak® multi-nutrient supplement had significant increases in their 2-HE:16alpha-HE ratio, which appears to be mediated primarily by increasing the 2-HE levels. These results suggest further research on phytonutrients that might positively affect estrogen metabolism is warranted.
Gynecological cancers are among the most common in women and are directly related to a variety of hormones. One potential risk for developing a gynecological malignancy is the relative ratio of two hormone metabolites, 2-Hydroxyestrone (2-HE) and 16alpha-Hydroxyestrone (16alpha-HE). Several early studies showed no significant difference in this 2-HE/16alpha-HE ratio between women currently with or without breast cancer [1–3]. However, more recent studies, including a longitudinal evaluation, showed that a higher ratio lowers the risk of developing future gynecological cancers [4, 5]. Approaches that positively affect this ratio could have important implications for patients at risk of developing gynecological cancers.
Several naturally occurring, plant-derived compounds have been investigated for increasing the 2-HE/16alpha-HE ratio. Indoles may help increase this ratio; in particular, indole-3-carbinol (I3C), a natural compound derived by hydrolysis from glycobrassicin produced in cruciferous vegetables such as cabbage, broccoli, and Brussels sprouts, and its natural diindole condensation product 3-3’-diindolylmethane (DIM) . Several studies provide evidence that both of these indoles can improve the 2-HE/16alpha-HE ratio when given in the appropriate dose . DIM, can induce estrogenic responses through a ligand-independent activation of estrogen receptors or disrupt estrogen responsiveness through its interaction with the aryl hydrocarbon receptor [8, 9].
Bioflavonoids have also been found to have anti-proliferative properties [10–12] that are mediated by several mechanisms. For example, bioflavonoids can interfere with several different free radical–producing systems and can also increase the function of the endogenous antioxidants  and can also inhibit cell proliferation and angiogenesis [14, 15]. However, it is not clear whether bioflavonoids specifically alter the 2-HE/16alpha-HE ratio. Another compound, resveratrol, has been shown to regulate estrogen effects also possibly conferring a beneficial effect with regard to the development of malignancy [16–18]. Several other herbal supplements might have beneficial effects as well. For example, icariin, a prenyl flavonoid derivative from Epimedium Genus has been shown to induce cell cycle arrest in breast cancer cells  and also has estrogenic effects . Red clover has been shown to possess antioxidant and antiinflammatory activities, as well as inhibit angiogenesis and displaying anti-cancer properties . Black currant extracts have been shown to have a variety of phytochemicals that have anti-proliferative effects via multiple cellular mechanisms .
These studies and others have led to the development of multi-nutrient supplements that blend compounds such as these to help improve the hormonal ratio and reduce the proliferative state. The goal of the present study was to retrospectively evaluate the effects of a multi-nutrient supplement designed for this purpose.
All patients in a university hospital out-patient setting who received 2-HE/16alpha-HE assessments at two distinct time points between 2010 and 2012 were included in this study. We retrospectively evaluated the hormone metabolism ratio of 65 patients (mean age 54±9 years) receiving the multi-nutrient supplement, Lucentia Peak®, for dietary support and preventive care. Since this was a retrospective evaluation of existing clinical data, this study was deemed exempt from review by the Institution Review Board (IRB) at Thomas Jefferson University and was administratively approved as per IRB guidelines. The supplement contains a combination of resveratrol, diindolylmethane, epimedium, eucommia, passion flower, suma, damiana, red clover, black currant extract, white button mushroom, and also vitamin E and C, calcium, and magnesium. The exact contents are provided in Table 1. We compared these results to 11 patients (mean age 54±5 years) who chose not to take the supplement, but were willing to receive a follow-up ratio assessment as part of overall clinical care. This formed the control group for the comparison. The mean duration of treatment was 196±175 days. The mean time between evaluations for the treatment group was 288±343 days and for the control group was 891±531 days. A paired t-test was used to compare the changes in the 2-HE and 16alpha-HE measures as well as their ratio. In addition, comparison between the ratio changes for the two groups was also performed. Serum measures of the 2-HE/16alpha-HE ratio were used in this study (27).
The results are shown in Table 2 and demonstrate a significant increase in the 2-HE levels and in the 2-HE/16alpha-HE ratio in the treated group (p < 0.0001), but no change to either of these measures in the untreated group. On an individual basis, 54 patients given Lucentia Peak had an increase in their 2-HE/16alpha-HE ratio (i.e. improvement), while 11 patients had a decrease (worsening). In the control group, 3 patients had an increase in their 2-HE/16alpha-HE ratio and 8 patients had a decrease. Overall, the treated group had a mean increase in the 2-HE/16alpha-HE ratio of 18 points (50%) while the control group had a decrease of 1 point. This difference between the treated and control group change in the ratio was statistically significant (p=0.02) based on a t-test comparing the change between the treated and control groups.
The results from the current study demonstrated that women who received the Lucentia Peak® multi-nutrient supplement had substantial improvements in their 2-HE:16alpha-HE ratio, and this appears to be mediated primarily by increasing the 2-HE levels. These results were comparable to another study that gave indole-3-carbinol to women at high risk for breast cancer . In that study, 17 women were evaluated and treated with increasing doses of indole-3-carbinol for 4 weeks. Patients receiving 800 mg per day demonstrated elevation in the CYP1A2 activity, which mirrored a 66% increase in the urinary 2-HE/16alpha-HE ratio in response to I3C. In that study, the maximal increase was observed with the 400 mg daily of I3C, with no further increase found at 800 mg daily. In a related study, Wong et al. demonstrated in 57 women that 300 mg per day of I3C significantly increased the 2-HE/16alpha-HE ratio . Additionally, the other indole, DIM has antitumorogenesis effects  in breast cancer. And a small placebo controlled study of 19 women given 108 mg DIM/day for 30 days showed a significant increase in levels of 2-HE (P=0. 020) even though the limited sample revealed a nonsignificant increase of 47% in the 2-OHE/16alpha-OHE ratio (P=0.059) .
Studies of the other compounds in Lucentia Peak® also have revealed potential anti-cancer effects mediated either through hormonal effects or other physiological processes. For example, resveratrol has been shown to inhibit estrogen-DNA adduct formation via its antioxidant function and to do so approximately 50% more effectively than N-acetyl cysteine . Icaritin, a prenyl flavonoid derivative from Epimedium Genus has been shown to induce cell cycle arrest in breast cancer cell lines in vitro and to have estrogenic effects in rat studies . Other compounds with estrogenic effects such as red clover are frequently used by women with breast cancer . However, their effectiveness is not established. Finally, several components in Lucentia Peak® also may alter the expression of various inflammatory biomarkers. Such anti-inflammatory properties might play an important role in the potential anti-tumorogenesis effects of this multi-nutrient supplement [11, 13, 21, 22].
Limitations of this study include that it was a retrospective evaluation. Future randomized, prospective and controlled trials will be necessary to better determine whether multi-nutrient supplements help reduce the 2-HE/16alpha-HE ratio, and subsequently, the risk of gynecological cancers. A placebo control would be particularly important, especially in those patients with low 2-HE/16alpha-HE ratios so that it can be more clearly determined whether the supplement has a definitive effect. Selection bias is a consideration since the treated group generally had lower values for the 2-HE/16alpha-HE ratio and therefore may have been given more encouragement by their treating physician to utilize the supplement for this purpose. However, it is noted that the 2-HE/16alpha-HE ratios for the untreated group did not change substantially.
Overall, this study showed that women with a low 2-HE/16alpha-HE ratio who were given Lucentia Peak® experienced an increase in the ratio, specifically related to an increase in the measure of 2-HE. Given the potential reduction in the risk of gynecological cancer in patients having a higher level of 2-HE and the hormone ratio, this study is an important step in evaluating a dietary supplements that may have implications for women’s preventive health.
Cauley JA, Zmuda JM, Danielson ME, Ljung BM, Bauer DC, Cummings SR, Kuller LH: Estrogen metabolites and the risk of breast cancer in older women. Epidemiology. 2003, 14: 740-744. 10.1097/01.ede.0000091607.77374.74.
Ursin G, London S, Stanczyk FZ, Gentzschein E, Paganini-Hill A, Ross RK, Pike MC: Urinary 2-hydroxyestrone/16alpha-hydroxyestrone ratio and risk of breast cancer in postmenopausal women. J Natl Cancer Inst. 1999, 91: 1067-1072. 10.1093/jnci/91.12.1067.
Obi N, Vrieling A, Heinz J, Chang-Claude J: Estrogen metabolite ratio: Is the 2-hydroxyestrone to 16α-hydroxyestrone ratio predictive for breast cancer?. Int J Womens Health. 2011, 3: 37-51.
Fuhrman BJ, Schairer C, Gail MH, Boyd-Morin J, Xu X, Sue LY, Buys SS, Isaacs C, Keefer LK, Veenstra TD, Berg CD, Hoover RN, Ziegler RG: Estrogen metabolism and risk of breast cancer in postmenopausal women. J Natl Cancer Inst. 2012, 104: 326-339. 10.1093/jnci/djr531.
Muti P, Bradlow HL, Micheli A, Krogh V, Freudenheim JL, Schünemann HJ, Stanulla M, Yang J, Sepkovic DW, Trevisan M, Berrino F: Estrogen metabolism and risk of breast cancer: a prospective study of the 2:16alpha-hydroxyestrone ratio in premenopausal and postmenopausal women. Epidemiology. 2000, 11: 635-640. 10.1097/00001648-200011000-00004.
Firestone GL, Sundar SN: Minireview: modulation of hormone receptor signaling by dietary anticancer indoles. Mol Endocrinol. 2009, 23: 1940-1947. 10.1210/me.2009-0149.
Wong GY, Bradlow L, Sepkovic D, Mehl S, Mailman J, Osborne MP: Dose-ranging study of indole-3-carbinol for breast cancer prevention. J Cell Biochem Suppl. 1997, 28–29: 111-116.
Wormke M, Stoner M, Saville B, Walker K, Abdelrahim M, Burghardt R, Safe S: The aryl hydrocarbon receptor mediates degradation of estrogen receptor through activation of proteasomes. Mol Cell Biol. 2003, 23: 1843-1855. 10.1128/MCB.23.6.1843-1855.2003.
Okino ST, Pookot D, Basak S, Dahiya R: Toxic and chemopreventive ligands preferentially activate distinct aryl hydrocarbon receptor pathways: implications for cancer prevention. Cancer Prev Res. 2009, 2: 251-256. 10.1158/1940-6207.CAPR-08-0146.
Manthey JA, Guthrie N: Antiproliferative activities of citrus flavonoids against six human cancer cell lines. J Agric Food Chem. 2002, 50: 5837-5843. 10.1021/jf020121d.
Mercader AG, Pomilio AB: Naturally-occurring dimers of flavonoids as anticarcinogens. Anticancer Agents Med Chem. 2013, [Epub ahead of print]
Wani BA, Ramamoorthy D, Rather MA, Arumugam N, Qazi AK, Majeed R, Hamid A, Ganie SA, Ganai BA, Anand R, Gupta AP: Induction of apoptosis in human pancreatic MiaPaCa-2 cells through the loss of mitochondrial membrane potential (ΔΨm) by Gentiana kurroo root extract and LC-ESI-MS analysis of its principal constituents. Phytomedicine. 2013, 20: 723-733. 10.1016/j.phymed.2013.01.011.
Nijveldt RJ, van Nood E, van Hoorn DE, Boelens PG, van Norren K, van Leeuwen PA: Flavonoids: a review of probable mechanisms of action and potential applications. Am J Clin Nutr. 2001, 74: 418-425.
Stefani ED, Boffetta P, Deneo-Pellegrini H, Mendilaharsu M, Carzoglio JC, Ronco A, Olivera L: Dietary antioxidants and lung cancer risk: a case–control study in Uruguay. Nutr Cancer. 1999, 34: 100-110. 10.1207/S15327914NC340114.
Fotsis T, Pepper MS, Aktas E, Breit S, Rasku S, Adlercreutz H, Wähälä K, Montesano R, Schweigerer L: Flavonoids, dietary-derived inhibitors of cell proliferation and in vitro angiogenesis. Cancer Res. 1997, 57: 2916-2921.
Reed GA, Peterson KS, Smith HJ, Gray JC, Sullivan DK, Mayo MS, Crowell JA, Hurwitz A: A phase I study of indole-3-carbinol in women: tolerability and effects. Cancer Epidemiol Biomarkers Prev. 2005, 14: 1953-1960. 10.1158/1055-9965.EPI-05-0121.
Eliassen AH, Spiegelman D, Xu X, Keefer LK, Veenstra TD, Barbieri RL, Willett WC, Hankinson SE, Ziegler RG: Urinary estrogens and estrogen metabolites and subsequent risk of breast cancer among premenopausal women. Cancer Res. 2012, 72: 696-706. 10.1158/0008-5472.CAN-11-2507.
So FV, Guthrie N, Chambers AF, Carroll KK: Inhibition of proliferation of estrogen receptor-positive MCF-7 human breast cancer cells by flavonoids in the presence and absence of excess estrogen. Cancer Lett. 1997, 112: 127-133. 10.1016/S0304-3835(96)04557-0.
Guo Y, Zhang X, Meng J, Wang ZY: An anticancer agent icaritin induces sustained activation of the extracellular signal-regulated kinase (ERK) pathway and inhibits growth of breast cancer cells. Eur J Pharmacol. 2011, 658: 114-122. 10.1016/j.ejphar.2011.02.005.
Yap SP, Shen P, Li J, Lee LS, Yong EL: Molecular and pharmacodynamic properties of estrogenic extracts from the traditional Chinese medicinal herb, Epimedium. J Ethnopharmacol. 2007, 113: 218-224. 10.1016/j.jep.2007.05.029.
Kolodziejczyk-Czepas J: Trifolium species-derived substances and extracts–biological activity and prospects for medicinal applications. J Ethnopharmacol. 2012, 143: 14-23. 10.1016/j.jep.2012.06.048.
Gopalan A, Reuben SC, Ahmed S, Darvesh AS, Hohmann J, Bishayee A: The health benefits of blackcurrants. Food Funct. 2012, 3: 795-809. 10.1039/c2fo30058c.
Hong C, Kim HA, Firestone GL, Bjeldanes LF: 3,3'-Diindolylmethane (DIM) induces a G(1) cell cycle arrest in human breast cancer cells that is accompanied by Sp1-mediated activation of p21(WAF1/CIP1) expression. Carcinogenesis. 2002, 23: 1297-1305. 10.1093/carcin/23.8.1297.
Dalessandri KM, Firestone GL, Fitch MD, Bradlow HL, Bjeldanes LF: Pilot study: effect of 3,3'-diindolylmethane supplements on urinary hormone metabolites in postmenopausal women with a history of early-stage breast cancer. Nutr Cancer. 2004, 50: 161-167. 10.1207/s15327914nc5002_5.
Zahid M, Saeed M, Beseler C, Rogan EG, Cavalieri EL: Resveratrol and N-acetylcysteine block the cancer-initiating step in MCF-10F cells. Free Radic Biol Med. 2011, 50: 78-85. 10.1016/j.freeradbiomed.2010.10.662.
McLay JS, Stewart D, George J, Rore C, Heys SD: Complementary and alternative medicines use by Scottish women with breast cancer. What, why and the potential for drug interactions?. Eur J Clin Pharmacol. 2012, 68: 811-819. 10.1007/s00228-011-1181-6.
AJB is a shareholder in the company that distributes the product, Lucentia Peak®. GPZ has no conflict of interest to report. ABN has no conflict of interest to report.
AJB treated the patients, helped obtain and evaluate the data, and drafted the manuscript. GZ helped with data analysis and drafting the manuscript. ABN participated in the design of the study and performed the statistical analysis as well as drafting the manuscript. All authors read and approved the final manuscript.
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Bazzan, A.J., Zabrecky, G.P. & Newberg, A.B. Multi-nutrient supplement improves hormone ratio associated with cancer risk. J Transl Med 11, 252 (2013). https://doi.org/10.1186/1479-5876-11-252