Université Lille 1, EA4478, F-59650 Villeneuve d'Ascq, France.
Bioorg Med Chem Lett. 2013 Jan 15;23(2):574-8. doi: 10.1016/j.bmcl.2012.11.009. Epub 2012 Nov 22.
Caffeic acid derivatives are increasingly regarded as potential oncoprotective that could inhibit both the initiation and progression of cancer. Here we have synthesized seven 1-arylnaphthalene lignans and related compounds and tested their impact on breast cancer cell growth in tissue culture. The product of the oxidative dimerization of methyl caffeate, 1-phenylnaphthalene lignan, was found to induce a strong decrease in breast cancer cell number (IC(50) ~1 μM) and was selected for further investigation. Flow cytometry analysis revealed a decrease in cell proliferation and an increase in apoptosis in both MCF-7 and MDA-MB-231 breast cancer cell lines that are representative of the two main categories of breast tumors. The 3,4-dihydroxyphenyl group probably induced the biological activity, as the control compounds lacking it had no effect on breast cancer cells. Together, our data indicate that the oxidative dimerization product of methyl caffeate can inhibit breast cancer cell growth at a concentration adequate for pharmacological use.
咖啡酸衍生物被越来越多地认为是具有潜在抗肿瘤作用的物质,能够抑制癌症的发生和发展。在这里,我们合成了七种 1-芳基萘烷木脂素及其相关化合物,并在组织培养中测试了它们对乳腺癌细胞生长的影响。咖啡酸甲酯氧化二聚产物 1-苯基萘烷木脂素被发现能强烈诱导乳腺癌细胞数量减少(IC50~1μM),因此被选择进行进一步研究。流式细胞术分析显示,在 MCF-7 和 MDA-MB-231 两种乳腺癌细胞系中,细胞增殖减少,凋亡增加,这两种细胞系代表了乳腺癌的两种主要类型。3,4-二羟基苯基可能诱导了生物活性,因为缺乏该基团的对照化合物对乳腺癌细胞没有影响。总之,我们的数据表明,咖啡酸甲酯的氧化二聚产物可以在足以用于药理学的浓度下抑制乳腺癌细胞的生长。