Development of in vitro models for cellular and molecular studies in toxicology and chemoprevention.

K Macé, E A Offord, C C Harris, A M Pfeifer
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引用次数: 30

Abstract

Many natural dietary phytochemicals found compounds found in fruits, vegetables, spices and tea have been shown in recent years to be protective against cancer in various animal models. In the light of the potential impact of these compounds on human health it is important to elucidate the mechanisms involved. We therefore developed and characterized relevant in vitro models using immortalized human epithelial cell lines derived from target tissues in carcinogenesis, such as lung, liver and colon. Assays were established, allowing the evaluation of the cytotoxic and genotoxic effects of various procarcinogens, including nitrosamines, mycotoxins and heterocyclic amines on these metabolically-competent human epithelial cell lines. These cellular models appeared to be a useful tool to study the capacity of certain food components to block the initiation stage of carcinogenesis. The ability of carnosol and carnosic acid from rosemary as well as the synthetic dithiolethione, oltipraz, to block the formation of DNA adducts, and their effects on the expression of phase I and phase II enzymes was investigated. We have observed that both rosemary extracts and oltipraz inhibited benzo(a)pyrene- or aflatoxin B1-induced DNA adduct formation by strongly inhibiting CYP450 activities and inducing the expression of glutathione S-transferase. These results in human cell models give some insight into the different mechanisms involved in the chemopreventive action of both natural and synthetic compounds in relation to phase I and phase II enzymes.

体外毒理学和化学预防的细胞和分子研究模型的建立。
近年来,在各种动物模型中发现,水果、蔬菜、香料和茶叶中发现的许多天然膳食植物化学物质具有抗癌作用。鉴于这些化合物对人类健康的潜在影响,阐明所涉及的机制很重要。因此,我们开发并表征了相关的体外模型,使用永生化的人类上皮细胞系,这些细胞系来源于致癌的靶组织,如肺、肝和结肠。建立了检测方法,可以评估各种致癌物(包括亚硝胺、真菌毒素和杂环胺)对这些代谢能力强的人类上皮细胞系的细胞毒性和基因毒性作用。这些细胞模型似乎是研究某些食物成分阻断癌变起始阶段的能力的有用工具。研究了迷迭香鼠尾草醇和鼠尾草酸以及合成的二硫代硫代酮oltipraz对DNA加合物形成的抑制作用,以及它们对ⅰ期和ⅱ期酶表达的影响。我们观察到迷迭香提取物和oltipraz通过强烈抑制CYP450活性和谷胱甘肽s -转移酶的表达来抑制苯并(a)芘或黄曲霉毒素b1诱导的DNA加合物的形成。这些在人类细胞模型中的结果使我们对天然化合物和合成化合物与I期和II期酶有关的化学预防作用的不同机制有了一些了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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