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单萜类化合物对乳腺癌的预防与治疗

Prevention and therapy of mammary cancer by monoterpenes.

作者信息

Gould M N

机构信息

Department of Human Oncology, University of Wisconsin-Madison 53792, USA.

出版信息

J Cell Biochem Suppl. 1995;22:139-44. doi: 10.1002/jcb.240590818.

Abstract

Monoterpenes, found in a wide variety of plants, are a major component of plant essential oils. The unsubstituted monocyclic monoterpene limonene has been shown to prevent carcinogen-induced mammary cancer at both the initiation and the promotion/progression stages. This terpene also causes the complete regression of the majority of advanced rat mammary cancer when added to the diet. Modification of limonene by hydroxylation at various positions increases both its chemopreventive and therapeutic efficacy. For example, the naturally occurring hydroxylated limonene analog perillyl alcohol is 5-10 times more potent than limonene and has a similar therapeutic index. Several cellular, metabolic and molecular activities are associated with terpene exposure. These include induction of phase I and II hepatic detoxification enzymes, selective inhibition of protein isoprenylation, inhibition of CoQ synthesis, and induction of the mannose 6-phosphate/IGFII receptor and TGF beta. Due to the therapeutic efficacy of monoterpenes in experimental model systems, clinical evaluation of this class of compounds has begun in advanced cancer patients. A Phase I trial of limonene is in progress in the UK. Efforts in the US will target perillyl alcohol for Phase I testing. Pre-IND toxicology is currently being completed. Phase I trails are anticipated to begin in the Spring of 1995. We feel that the results of these therapeutic trials, if positive, will facilitate the development of current terpenes and more potent analogs for future chemoprevention trials.

摘要

单萜类化合物存在于多种植物中,是植物精油的主要成分。未被取代的单环单萜柠檬烯已被证明在致癌作用的起始阶段以及促进/进展阶段均能预防致癌物诱发的乳腺癌。当添加到饮食中时,这种萜类化合物还能使大多数晚期大鼠乳腺癌完全消退。通过在不同位置进行羟基化修饰柠檬烯,可提高其化学预防和治疗功效。例如,天然存在的羟基化柠檬烯类似物紫苏醇的效力比柠檬烯强5至10倍,且具有相似的治疗指数。萜类化合物的暴露与多种细胞、代谢和分子活性相关。这些包括诱导I相和II相肝脏解毒酶、选择性抑制蛋白质异戊二烯化、抑制辅酶Q合成以及诱导甘露糖6 - 磷酸/胰岛素样生长因子II受体和转化生长因子β。由于单萜类化合物在实验模型系统中的治疗功效,这类化合物已开始在晚期癌症患者中进行临床评估。英国正在进行柠檬烯的I期试验。美国的研究将以紫苏醇为目标进行I期测试。目前正在完成IND前毒理学研究。预计I期试验将于1995年春季开始。我们认为,如果这些治疗试验的结果是阳性的,将有助于开发目前的萜类化合物以及更有效的类似物用于未来的化学预防试验。

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