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大豆异黄酮对乳腺癌血管生成的影响:一种多重玻璃酶联免疫吸附测定方法

Influence of soy isoflavones in breast cancer angiogenesis: a multiplex glass ELISA approach.

作者信息

Uifalean Alina, Rath Hermann, Hammer Elke, Ionescu Corina, Iuga Cristina Adela, Lalk Michael

机构信息

Department of Pharmaceutical Analysis, Faculty of Pharmacy, "Iuliu Hațieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.

出版信息

J BUON. 2018 Dec;23(7):53-59.

Abstract

PURPOSE

The aim of this study was to evaluate the anti-angiogenic properties of soy isoflavones using two breast cancer cell lines, by measuring the concentration of 30 cytokines involved in angiogenesis using a multiplex glass slide ELISA-based array.

METHODS

Estrogen-dependent MCF-7 cells and estrogen-independent MDA-MB-231 cells were exposed to genistein (Gen), daidzein (Dai) and a soy seed extract (Ext) for 72 hrs, at selected concentration levels. The conditioned medium was analyzed using a glass slide, multiplex sandwich ELISA-based platform with fluorescent detection which allowed the identification and the quantification of 30 angiogenesis-related cytokines.

RESULTS

In MCF-7 cells, low, stimulatory concentrations of test compounds determined the increase of CXCL16 and VEGF-A level. Gen induced the greatest effect, with 1.5-fold change compared to control. When MDA-MB-231 cells were exposed to inhibitory concentrations, all test compounds determined a reduction of CXCL16 and VEGF-A level with approximately 30%.

CONCLUSIONS

Soluble CXCL16 and VEGF-A are two promoters of angiogenesis and metastasis in breast cancer. The stimulation of these two angiogenesis-related cytokines could represent one of the mechanisms explaining the proliferative effects of low isoflavone doses in estrogen-dependent cells. In estrogen-independent cells, soy isoflavones inhibited their secretion, demonstrating promising anti-angiogenic properties.

摘要

目的

本研究旨在通过使用基于多重玻片酶联免疫吸附测定(ELISA)阵列测量参与血管生成的30种细胞因子的浓度,来评估大豆异黄酮对两种乳腺癌细胞系的抗血管生成特性。

方法

将雌激素依赖性MCF-7细胞和雌激素非依赖性MDA-MB-231细胞在选定的浓度水平下暴露于染料木黄酮(Gen)、大豆苷元(Dai)和大豆种子提取物(Ext)72小时。使用基于多重夹心ELISA的荧光检测玻片平台分析条件培养基,该平台可识别和定量30种与血管生成相关的细胞因子。

结果

在MCF-7细胞中,低浓度的刺激性测试化合物可导致CXCL16和VEGF-A水平升高。染料木黄酮诱导的效果最显著,与对照组相比变化了1.5倍。当MDA-MB-231细胞暴露于抑制浓度时,所有测试化合物均使CXCL16和VEGF-A水平降低约30%。

结论

可溶性CXCL16和VEGF-A是乳腺癌血管生成和转移的两个促进因子。这两种与血管生成相关的细胞因子的刺激可能是解释低剂量异黄酮对雌激素依赖性细胞增殖作用的机制之一。在雌激素非依赖性细胞中,大豆异黄酮抑制了它们的分泌,显示出有前景的抗血管生成特性。

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