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The Journal of Nutrition Vol. 127 No. 5 May 1997, pp. 668-674
Copyright ©1997 by the American Society for Nutritional Sciences

Isoprenoids Suppress the Growth of Murine B16 Melanomas In Vitro and In Vivo

Manuscript received 17 September 1996. Initial reviews completed 30 October 1996. Revision accepted 23 December 1996.

Lei He, Huanbiao Mo, Susilowati Hadisusilo*, Asaf A. Qureshidagger , and Charles E. Elson

Department of Nutritional Sciences, University of Wisconsin, Madison, WI 53706; * Department of Chemistry, University of Indonesia, Depok, Jakarta, Indonesia; and dagger  Advanced Medical Research, Madison, WI 53719

Sundry mevalonate-derived constituents (isoprenoids) of fruits, vegetables and cereal grains suppress the growth of tumors. This study estimated the concentrations of structurally diverse isoprenoids required to inhibit the increase in a population of murine B16(F10) melanoma cells during a 48-h incubation by 50% (IC50 value). The IC50 values for d-limonene and perillyl alcohol, the monoterpenes in Phase I trials, were 450 and 250 µmol/L, respectively; related cyclic monoterpenes (perillaldehyde, carvacrol and thymol), an acyclic monoterpene (geraniol) and the end ring analog of beta -carotene (beta -ionone) had IC50 values in the range of 120-150 µmol/L. The IC50 value estimated for farnesol, the side-chain analog of the tocotrienols (50 µmol/L) fell midway between that of alpha -tocotrienol (110 µmol/L) and those estimated for gamma - (20µmol/L) and delta - (10 µmol/L) tocotrienol. A novel tocotrienol lacking methyl groups on the tocol ring proved to be extremely potent (IC50, 0.9 µmol/L). In the first of two diet studies, experimental diets were fed to weanling C57BL female mice for 10 d prior to and 28 d following the implantation of the aggressively growing and highly metastatic B16(F10) melanoma. The isomolar (116 µmol/kg diet) and the Vitamin E-equivalent (928 µmol/kg diet) substitution of d-gamma -tocotrienol for dl-alpha -tocopherol in the AIN-76A diet produced 36 and 50% retardations, respectively, in tumor growth (P < 0.05). In the second study, melanomas were established before mice were fed experimental diets formulated with 2 mmol/kg d-gamma -tocotrienol, beta -ionone individually and in combination. Each treatment increased (P < 0.03) the duration of host survival. Our finding that the effects of individual isoprenoids were additive suggests the possibility that one component of the anticarcinogenic action of plant-based diets is the tumor growth-suppressive action of the diverse isoprenoid constituents of fruits, vegetables and cereal grains.

Key words: mice, 3-hydroxy-3-methylglutaryl coenzyme A reductase, tocotrienols, monoterpenes, tumor implants.




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