Isoprenoid-mediated inhibition of mevalonate synthesis: Potential application to cancer

被引:114
作者
Elson, CE
Peffley, DM
Hentosh, P
Mo, HB
机构
[1] Univ Wisconsin, Dept Nutr Sci, Coll Agr & Life Sci, Madison, WI 53706 USA
[2] Finch Univ Hlth Sci Chicago Med Sch, Dept Mol & Cellular Pharmacol, N Chicago, IL 60064 USA
来源
PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE | 1999年 / 221卷 / 04期
关键词
D O I
10.1046/j.1525-1373.1999.d01-87.x
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Pure and mixed isoprenoid end products of plant mevalonate metabolism trigger actions that suppress 3-hydroxy-3-methylglutaryl coenzyme A (HMG CoA) reductase activity. These actions modulate HMG CoA reductase mRNA translation and the proteolytic degradation of HMG CoA reductase. Such post-transcriptional events, we propose, are activated directly by acyclic isoprenoids and indirectly by cyclic isoprenoids. Isoprenoids, acting secondarily to the dominant transcriptional effector of sterologenesis, modestly lower cholesterol levels, if and only if, sterologenesis is not repressed by a saturating imput of dietary cholesterol. An anomaly associated with tumor growth-a sterol feedback-resistant HMG CoA reductase activity-ensures a pool of sterologenic pathway intermediates. Such intermediates provide lipophilic anchors essential for membrane attachment and biological activity of growth hormone receptors, nuclear lamins A and B, and oncogenic res. Tumor HMG CoA reductase retains high sensitivity to the isoprenoid-mediated secondary regulation. Repression of mevalonate synthesis by plant-derived isoprenoids reduces res and lamin B processing, arrests cells in G1, and initiates cellular apoptosis. This unique tumor cell-specific sensitivity allows isoprenoids to be used for tumor therapy, an application emulating that of the statins, but one free of adverse effects. When evaluated at levels provided by a typical diet, isoprenoids individually have no impact on cholesterol synthesis and tumor growth. Nonetheless, isoprenoid-mediated activities are additive, and, sometimes synergistic. Therefore, the combined actions of the estimated 23,000 isoprenoid constituents of plant materials, acting in concert with other chemopreventive phytochemicals, may explain the lowered cancer risk associated with a diet rich in plant products. In contrast, that lowering of cancer risk does not correspond to supplemental intake of other dietary factors associated with fruits, vegetables, and cereal grains, namely fiber, beta-carotene, vitamin C, and vitamin E, and only weakly to supplemental folate.
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页码:294 / 311
页数:18
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共 314 条
  • [1] DIFFERENCES IN SENSITIVITY TO FARNESOL TOXICITY BETWEEN NEOPLASTICALLY-DERIVED AND NON-NEOPLASTICALLY-DERIVED CELLS IN CULTURE
    ADANY, I
    YAZLOVITSKAYA, EM
    HAUG, JS
    VOZIYAN, PA
    MELNYKOVYCH, G
    [J]. CANCER LETTERS, 1994, 79 (02) : 175 - 179
  • [2] alpha-tocopherol and beta-carotene supplements and lung cancer incidence in the Alpha-Tocopherol, Beta-Carotene Cancer Prevention Study: Effects of base-line characteristics and study compliance
    Albanes, D
    Heinonen, OP
    Taylor, PR
    Virtamo, J
    Edwards, BK
    Rautalahti, M
    Hartman, AM
    Palmgren, J
    Freedman, LS
    Haapakoski, J
    Barrett, MJ
    Pietinen, P
    Malila, N
    Tala, E
    Liippo, K
    Salomaa, ER
    Tangrea, JA
    Teppo, L
    Askin, FB
    Taskinen, E
    Erozan, Y
    Greenwald, P
    Huttunen, JK
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (21) : 1560 - 1570
  • [3] Alpha-Tocopherol Beta Carotene Cancer Prevention Study Group, 1994, N Engl J Med, V330, P1029, DOI 10.1056/NEJM199404143301501
  • [4] THE CAUSES AND PREVENTION OF CANCER
    AMES, BN
    GOLD, LS
    WILLETT, WC
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (12) : 5258 - 5265
  • [5] Identifying differential gene expression in monoterpene-treated mammary carcinomas using subtractive display
    Ariazi, EA
    Gould, MN
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (46) : 29286 - 29294
  • [6] THE EFFECT OF TERPENOID COMPOUNDS ON CYTOCHROME-P-450 LEVELS IN RAT-LIVER
    AUSTIN, CA
    SHEPHARD, EA
    PIKE, SF
    RABIN, BR
    PHILLIPS, IR
    [J]. BIOCHEMICAL PHARMACOLOGY, 1988, 37 (11) : 2223 - 2229
  • [7] CANCER PREVENTION IN PRIMARY-CARE - DIET AND CANCER .4.
    AUSTOKER, J
    [J]. BRITISH MEDICAL JOURNAL, 1994, 308 (6944) : 1610 - 1614
  • [8] A DISCOORDINATE INCREASE IN THE CELLULAR AMOUNT OF 3-HYDROXY-3-METHYLGLUTARYL-COA REDUCTASE RESULTS IN THE LOSS OF RATE-LIMITING CONTROL OVER CHOLESTEROGENESIS IN A TUMOR CELL-FREE SYSTEM
    AZROLAN, NI
    COLEMAN, PS
    [J]. BIOCHEMICAL JOURNAL, 1989, 258 (02) : 421 - 425
  • [9] SOME NEW ASPECTS OF ISOPRENOID BIOSYNTHESIS IN PLANTS - A REVIEW
    BACH, TJ
    [J]. LIPIDS, 1995, 30 (03) : 191 - 202
  • [10] CHARACTERIZATION OF 2 DISTINCT ALLYL PYROPHOSPHATASE ACTIVITIES FROM RAT-LIVER MICROSOMES
    BANSAL, VS
    VAIDYA, S
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1994, 315 (02) : 393 - 399