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联合植物化学物质对 SENCAR 小鼠皮肤癌的协同预防作用。

Synergistic effects of combined phytochemicals and skin cancer prevention in SENCAR mice.

机构信息

Department of Pharmacology, University of Texas Health Science Center at San Antonio, 78229, USA.

出版信息

Cancer Prev Res (Phila). 2010 Feb;3(2):170-8. doi: 10.1158/1940-6207.CAPR-09-0196. Epub 2010 Jan 26.

Abstract

The purpose of our study was to determine the inhibitory effect of combined phytochemicals on chemically induced murine skin tumorigenesis. Our hypothesis was that concurrent topical and dietary treatment with selected compounds would lead to more efficient prevention of skin cancer. We tested ellagic acid and calcium D-glucarate as components of diets, while resveratrol was applied topically; grape seed extract was applied topically or in the diet. The 4-week inflammatory-hyperplasia assay based on the 7,12-dimethylbenz[a]anthracene (DMBA)-induced skin carcinogenesis model in SENCAR mice was used. We have found that all the selected combinations caused a marked decrease of epidermal thickness compared with the DMBA-treated group and also with groups treated with a single compound and DMBA. All combinations of resveratrol with other compounds showed a synergistic effect on hyperplasia and Ha-ras mutations. Skin tissue of mice receiving the combinations showed decreased cell proliferation and Bcl2 expression; decreased p21, a regulator of cell cycle; and decreased marker of inflammation cyclooxygenase-2. All the selected combinations diminished the DMBA-induced mRNA expression of the CYP1B1 level, and also caused a marked decrease of proto-oncogenes c-jun and c-fos, components of transcription factor activator protein. In conclusion, all combinations showed either additive or synergistic effects and their joint actions allowed for decreasing the doses of the compounds. Especially, resveratrol combinations with ellagic acid, grape seed extract, and other phytochemicals are very potent inhibitors of skin tumorgenesis, based on the suppression of epidermal hyperplasia as well as on the modulation of intermediate biomarkers of cell proliferation, cell survival, inflammation, oncogene mutation, and apoptosis.

摘要

本研究的目的是确定联合植物化学物质对化学诱导的小鼠皮肤肿瘤发生的抑制作用。我们的假设是,同时进行局部和饮食治疗选定的化合物将导致更有效地预防皮肤癌。我们测试了鞣花酸和钙 D-葡萄糖醛酸作为饮食的成分,而白藜芦醇则局部应用;葡萄籽提取物局部或在饮食中应用。我们使用了基于 7,12-二甲基苯并[a]蒽(DMBA)诱导的 SENCAR 小鼠皮肤致癌模型的 4 周炎症增生测定法。我们发现,与 DMBA 处理组以及单独用一种化合物和 DMBA 处理的组相比,所有选定的组合都导致表皮厚度明显减少。白藜芦醇与其他化合物的所有组合对增生和 Ha-ras 突变均显示协同作用。接受组合治疗的小鼠皮肤组织显示细胞增殖和 Bcl2 表达减少;细胞周期调节剂 p21 减少;炎症标志物环氧合酶-2 减少。所有选定的组合均降低了 DMBA 诱导的 CYP1B1 水平的 mRNA 表达,并且还导致原癌基因 c-jun 和 c-fos 的明显减少,这是转录因子激活蛋白的组成部分。总之,所有组合均显示出相加或协同作用,它们的联合作用允许减少化合物的剂量。特别是白藜芦醇与鞣花酸、葡萄籽提取物和其他植物化学物质的组合,基于对表皮增生的抑制以及对细胞增殖、细胞存活、炎症、癌基因突变和凋亡的中间生物标志物的调节,是非常有效的皮肤肿瘤抑制剂。

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