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类异戊二烯介导的甲羟戊酸合成抑制:在癌症中的潜在应用。

Isoprenoid-mediated inhibition of mevalonate synthesis: potential application to cancer.

作者信息

Elson C E, Peffley D M, Hentosh P, Mo H

机构信息

Department of Nutritional Sciences, College of Agricultural and Life Sciences, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

出版信息

Proc Soc Exp Biol Med. 1999 Sep;221(4):294-311. doi: 10.1046/j.1525-1373.1999.d01-87.x.

Abstract

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 ras. Tumor HMG CoA reductase retains high sensitivity to the isoprenoid-mediated secondary regulation. Repression of mevalonate synthesis by plant-derived isoprenoids reduces ras 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.

摘要

植物甲羟戊酸代谢产生的纯类异戊二烯和混合类异戊二烯终产物会引发抑制3-羟基-3-甲基戊二酰辅酶A(HMG CoA)还原酶活性的作用。这些作用调节HMG CoA还原酶mRNA的翻译以及HMG CoA还原酶的蛋白水解降解。我们认为,此类转录后事件直接由无环类异戊二烯激活,间接由环状类异戊二烯激活。类异戊二烯在甾醇生成的主要转录效应物之后起作用,仅在膳食胆固醇饱和输入不抑制甾醇生成的情况下,适度降低胆固醇水平。与肿瘤生长相关的一种异常情况——一种对甾醇反馈有抗性的HMG CoA还原酶活性——确保了甾醇生成途径中间产物的储备。此类中间产物为生长激素受体、核纤层蛋白A和B以及致癌性ras蛋白的膜附着和生物活性提供了必需的亲脂性锚定物。肿瘤HMG CoA还原酶对类异戊二烯介导的二级调节保持高度敏感性。植物来源的类异戊二烯对甲羟戊酸合成的抑制作用会减少ras和核纤层蛋白B的加工,使细胞停滞在G1期,并引发细胞凋亡。这种独特的肿瘤细胞特异性敏感性使得类异戊二烯可用于肿瘤治疗,这一应用类似于他汀类药物,但没有副作用。当按照典型饮食所提供的水平进行评估时,类异戊二烯单独对胆固醇合成和肿瘤生长没有影响。尽管如此,类异戊二烯介导的活性具有加和性,有时还具有协同性。因此,植物材料中估计23,000种类异戊二烯成分与其他化学预防植物化学物质协同发挥的联合作用,可能解释了富含植物产品的饮食与降低癌症风险之间的关联。相比之下,癌症风险的降低与水果、蔬菜和谷物中其他膳食因素(即纤维、β-胡萝卜素、维生素C和维生素E)的补充摄入并不对应,与补充叶酸的关联也很弱。

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