Methods of analysis for chemicals that disrupt cellular signaling pathways: risk assessment for potential endocrine disruptors.

Yoshio Umezawa, Takeaki Ozawa, Moritoshi Sato, Hidekuni Inadera, Shuichi Kaneko, Manabu Kunimoto, Shin-ichi Hashimoto
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Abstract

Here we present a basic concept and several examples of methods of analysis for chemicals that disrupt cellular signaling pathways, in view of risk assessment for potential endocrine disrupting chemicals (EDCs). The key cellular signaling pathways include 1) ER/coactivator interaction, 2) AR translocation into the nucleus, 3) ER/NO/sGC/cGMP, 4) ER/Akt, 5) ER/Src, 6)ER/Src/Grb2, and 7) ER/Ca2+/CaM/CaMK pathways. These were visualized in relevant live cells using newly developed fluorescent and bioluminescent probes. Changes in cellular signals were thereby observed in nongenomic pathways of steroid hormones upon treatment of the target cells with steroid hormones and related chemicals. This method of analysis appears to be a rational approach to high-throughput prescreening (HTPS) of biohazardous chemicals, EDCs, in particular. Also described was the screening of gene expression by serial analysis of gene expression and gene chips upon applying EDCs to breast cancer cells, mouse livers, and human neuroblastoma NB-1 cells.

破坏细胞信号通路的化学物质的分析方法:潜在内分泌干扰物的风险评估。
鉴于潜在内分泌干扰物质(EDCs)的风险评估,我们提出了一个基本概念和几个分析方法的例子,这些方法破坏了细胞信号通路。关键的细胞信号通路包括1)ER/共激活因子相互作用,2)AR转运到细胞核,3)ER/NO/sGC/cGMP, 4) ER/Akt, 5) ER/Src, 6)ER/Src/Grb2和7)ER/Ca2+/CaM/CaMK途径。使用新开发的荧光和生物发光探针在相关活细胞中观察这些细胞。因此,在用类固醇激素和相关化学物质处理靶细胞后,在类固醇激素的非基因组途径中观察到细胞信号的变化。这种分析方法似乎是生物有害化学品,特别是EDCs的高通量预筛选(HTPS)的合理方法。同时描述了EDCs应用于乳腺癌细胞、小鼠肝脏和人神经母细胞瘤NB-1细胞后,通过基因表达序列分析和基因芯片筛选基因表达。
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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