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Cancer Research 68, 4384, June 1, 2008. doi: 10.1158/0008-5472.CAN-08-0108
© 2008 American Association for Cancer Research

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Experimental Therapeutics, Molecular Targets, and Chemical Biology

Interaction of Tomato Lycopene and Ketosamine against Rat Prostate Tumorigenesis

Valeri V. Mossine1, Pankaj Chopra1 and Thomas P. Mawhinney1,2

Departments of 1 Biochemistry and 2 Child Health, University of Missouri-Columbia, Columbia, Missouri

Requests for reprints: Valeri V. Mossine, Department of Biochemistry, University of Missouri-Columbia, Agriculture Building, Room 4, Columbia, MO 65211. Phone: 573-882-2608; Fax: 573-884-4631; E-mail: MossineV{at}missouri.edu.

Key Words: Prostate Cancer • Prevention • Tomato • Ketosamine • Antioxidant

Prior investigations on the beneficial effect of dietary processed tomato products and lycopene on prostate cancer risk suggested that lycopene may require the presence of other constituents to exert its chemopreventive potential. We investigated whether ketosamines, a group of carbohydrate derivatives present in dehydrated tomato products, may interact with lycopene against prostate tumorigenesis. One ketosamine, FruHis, strongly synergized with lycopene against proliferation of the highly metastatic rat prostate adenocarcinoma MAT-LyLu cell line in vitro. The FruHis/lycopene combination significantly inhibited in vivo tumor formation by MAT-LyLu cells in syngeneic Copenhagen rats. Energy-balanced diets, supplemented with tomato paste, tomato powder, or tomato paste plus FruHis, were fed to Wistar-Unilever rats (n = 20 per group) treated with N-nitroso-N-methylurea and testosterone to induce prostate carcinogenesis. Survival from carcinogenesis was lowest in the control group (median survival time, 40 weeks) and highest in the group fed the tomato paste/FruHis diet (51 weeks; P = 0.004, versus control). The proportions of dying rats with macroscopic prostate tumors in the control, tomato paste, tomato powder, and tomato paste/FruHis groups were 63% (12 of 19), 39% (5 of 13), 43% (6 of 14), and 18% (2 of 11), respectively. FruHis completely blocked DNA oxidative degradation at >250 µmol/L in vitro, whereas neither ascorbate nor phenolic antioxidants from tomato were effective protectors in this assay. FruHis, therefore, may exert tumor-preventive effect through its antioxidant activity and interaction with lycopene. [Cancer Res 2008;68(11):4384–91]




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
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Molecular Cancer Research Cancer Prevention Research
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Copyright © 2008 by the American Association for Cancer Research.