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Possible synergistic prostate cancer suppression by anatomically discrete pomegranate fractionsJournal Investigational New Drugs Publisher Springer Netherlands ISSN 0167-6997 (Print) 1573-0646 (Online) Issue Volume 23, Number 1 / January, 2005 DOI 10.1023/B:DRUG.0000047101.02178.07 Pages 11-20 Subject Collection Medicine SpringerLink Date Tuesday, December 07, 2004 Possible synergistic prostate cancer suppression by anatomically discrete pomegranate fractionsEphraim P. Lansky1
, Wenguo Jiang2, Huanbiao Mo3, Lou Bravo3, Paul Froom4, Weiping Yu5, Neil M. Harris6, Ishak Neeman7 and Moray J. Campbell8(1) Rimonest Ltd., Horev Center, Box, 9945, Haifa, Israel (2) University Department of Surgery, University of Wales College of Medicine, Cardiff, UK (3) Department of Nutrition and Food Science, Texas Women's University, Denton, TX, USA (4) Department of Epidemiology and Preventive Medicine, Sackler Medical School, Tel Aviv University, Tel Aviv, Israel (5) School of Biological Sciences, University of Texas at Austin, Austin, TX, USA (6) Department of Urology, Royal Bournemouth Hospital, Bournemouth, UK (7) Department of Food Engineering and Biotechnology, Technion—Israel Institute of Technology, Haifa, Israel (8) Division of Medical Sciences, University of Birmingham Medical School, Birmingham, UK Abstract We investigated whether dissimilar biochemical fractions originating in anatomically discrete sections of the pomegranate (Punica granatum) fruit might act synergistically against proliferation, metastatic potential, and phosholipase A2 (PLA2) expression of human prostate cancer cells in vitro. Proliferation of DU 145 human prostate cancer cells was measured following treatment with a range of therapeutically active doses of fermented pomegranate juice polyphenols (W) and sub-therapeutic doses of either pomegranate pericarp (peel) polyphenols (P) or pomegranate seed oil (Oil). Invasion across Matrigel by PC-3 human prostate cancer cells was measured following treatment with combinations of W, P and Oil such that the total gross weight of pomegranate extract was held constant. Expression of PLA2, associated with invasive potential, was measured in the PC-3 cells after treatment with the same dosage combinations as per invasion. Supra-additive, complementary and synergistic effects were proven in all models by the Kruskal-Wallis non-parametric H test at p < 0.001 for the proliferation tests, p < 0.01 for invasion, and p < 0.05 for PLA2 expression. Proliferation effects were additionally evaluated with CompuSyn software median effect analysis and showed a concentration index CI < 1, confirming synergy. The results suggest vertical as well as the usual horizontal strategies for discovering pharmacological actives in plants.botanical - chaos - chemoprevention - complex drug - complexity - drug design - drug discovery - natural product

Ephraim P. Lansky
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