Shen Wenyan, Liu Hui, Yu Yingnian
Department of Pathophysiology, Zhejiang University, School of Medicine, Hangzhou 310058, China.
J Proteome Res. 2007 Dec;6(12):4737-48. doi: 10.1021/pr070406b. Epub 2007 Nov 1.
Benzo(a)pyrene is an ubiquitous environmental carcinogen produced during incomplete combustion of organic substances, and anti-benzo(a)pyrene-7,8-dihydrodiol-9,10-epoxide (BPDE), is the most carcinogenic form of its ultimate metabolites. The goal of this study was to examine the response of human amniotic epithelial FL cells to increasing concentrations of BPDE and to find potential biomarkers involved in this cellular response. Human amniotic epithelial FL cells were incubated with 0.005, 0.05, and 0.5 microM BPDE to obtain protein extracts which were resolved by two-dimensional electrophoresis (2-DE) and visualized by silver staining. More than 60 protein spots significantly changed after BPDE exposure. Among these, 2 spots were detected only in the exposed group, and 36 spots were up-regulated, while 27 spots were down-regulated. These altered spots were excised from the gels and analyzed by matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry (MALDI-TOF-MS). The analysis led to the identification of 46 proteins affected by BPDE. These proteins were involved in regulation of transcription, cell cycle, cell proliferation, transport, signal transduction, metabolism, and so forth. However, no single protein changed in a dose-dependent manner in all three concentrations. Therefore, the changes of proteomic profiles cannot be considered as only an amplification of low-dose response in the case of high-dose exposure and the cellular responses to different doses of DNA damaging agent may be quite different. These results will aid our understanding of the mechanism of BPDE-induced cell response and provide the possibility of the establishment of potential biomarkers.
苯并(a)芘是有机物质不完全燃烧过程中产生的一种普遍存在的环境致癌物,而反式苯并(a)芘-7,8-二氢二醇-9,10-环氧化物(BPDE)是其最终代谢产物中最具致癌性的形式。本研究的目的是检测人羊膜上皮FL细胞对不同浓度BPDE的反应,并寻找参与这种细胞反应的潜在生物标志物。将人羊膜上皮FL细胞与0.005、0.05和0.5微摩尔/升的BPDE孵育,以获得蛋白质提取物,通过二维电泳(2-DE)进行分离,并用银染法进行可视化。BPDE暴露后,60多个蛋白质斑点发生了显著变化。其中,2个斑点仅在暴露组中检测到,36个斑点上调,27个斑点下调。从凝胶中切下这些变化的斑点,通过基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF-MS)进行分析。分析鉴定出46种受BPDE影响的蛋白质。这些蛋白质参与转录调控、细胞周期、细胞增殖、转运、信号转导、代谢等过程。然而,在所有三种浓度下,没有一种蛋白质以剂量依赖的方式发生变化。因此,在高剂量暴露的情况下,蛋白质组学图谱的变化不能仅仅被视为低剂量反应的放大,细胞对不同剂量DNA损伤剂的反应可能有很大差异。这些结果将有助于我们理解BPDE诱导细胞反应的机制,并为建立潜在生物标志物提供可能性。