Proteome analysis of responses to ascochlorin in a human osteosarcoma cell line by 2-D gel electrophoresis and MALDI-TOF MS

被引:29
|
作者
Kang, Jeong Han
Park, Kwan-Kyu
Lee, In-Seon
Magae, Junji
Ando, Kunio
Kim, Cheorl-Ho
Chang, Young-Chae
机构
[1] Catholic Univ Daegu, Sch Med, Dept Pathol, Taegu 705034, South Korea
[2] Keimyung Univ, Ctr Tradit Microorganism Resources, TMR, Taegu 704701, South Korea
[3] Inst Res & Innovat, Dept Biotechnol, Kashiwa, Chiba 2770861, Japan
[4] NRL Pharma Inc, Kawasaki 2130012, Japan
[5] Sungkyunkwan Univ, Dept Biol Sci, Suwon 440746, Kyunggi, South Korea
关键词
ascochlorin; human osteosarcoma cells; 2-D gel; MALDI-TOF-MS;
D O I
10.1021/pr060111i
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Ascochlorin is a prenyl-phenol compound that was isolated from the fungus Ascochyta viciae. Ascochlorin reduces serum cholesterol and triglyceride levels, suppresses hypertension and tumor development, and ameliorates type I and II diabetes. Here, to better understand the mechanisms by which ascochlorin regulates physiological or pathological events and induces responses in the pharmacological treatment of cancer, we performed differential analysis of the proteome of the human osteosarcoma cells U2OS in response to ascochlorin. In addition, we established the first two-dimensional map of the U2OS proteome. The U2OS cell proteomes with and without treatment with ascochlorin were compared using two-dimensional electrophoresis, matrix-assisted laser desorption/ionization mass spectrometry and bioinformatics. The largest differences in expression were observed for the epidermal growth factor receptor (4-fold decrease), ribulose-5-phosphate-epimerase (13-fold decrease), ATP-dependent RNA helicase (8-fold decrease), and kelch-like ECH-associated protein 1 (6-fold decrease). The abundance of heterogeneous nuclear ribonucleoprotein L and minichromosome maintenance protein 7 increased 12- and 8.2-fold, respectively. In addition, Erk 2 was increased 3-fold in U2OS cells treated with ascochlorin. The expression of some selected proteins was confirmed by western blotting, zymography and RT-PCR analysis.
引用
收藏
页码:2620 / 2631
页数:12
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