Suppr超能文献

通过二维凝胶电泳检测膀胱癌细胞系中与顺铂耐药相关的蛋白质表达谱。

Protein expression profile related to cisplatin resistance in bladder cancer cell lines detected by two-dimensional gel electrophoresis.

作者信息

Taoka Yoshinori, Matsumoto Kazumasa, Ohashi Kazuya, Minamida Satoru, Hagiwara Masahiro, Nagi Shoji, Saito Tatsuya, Kodera Yoshio, Iwamura Masatsugu

机构信息

Department of Urology, Kitasato University School of Medicine.

出版信息

Biomed Res. 2015;36(4):253-61. doi: 10.2220/biomedres.36.253.

Abstract

We used a proteomic approach to compare the differentially regulated protein expression profiles of cisplatin-naïve and cisplatin-resistant bladder cancer cell lines to screen candidate molecules related to cisplatin resistance. The cisplatin-resistant cell line T24 was established by the stepwise exposure of T24 cells to up to 40 μM of cisplatin. We performed a comprehensive study of protein expression in bladder cancer cell lines that included cisplatin-naïve (T24) and cisplatin-resistant cells (T24CDDPR) by means of agarose two-dimensional gel electrophoresis followed by analysis of liquid chromatography tandem mass spectroscopy. We identified 25 obviously different spots for T24 and T24 CDDPR. Seven spots had increased expression and 18 spots had decreased expression in T24CDDPR compared to those in T24. Cytoskeletal proteins and enzyme modulators were prominent among differential proteins. Of the 25 proteins, we selected HNRNPA3, PCK2, PPL, PGK1, TKT, SERPINB2, GOT2, and EIF3A for further validation by Western blot. HNRNPA3, PGK1, TKT, and SERPINB2 had more than 1.5-times incremental expression in T24CDDPR compared to that in T24. PCK2 and PPL expressions were decreased less than 20% in T24CDDPR compared to that in T24. The results of 25 new proteins in this study could be valuable and could lead to the development of a new molecular marker.

摘要

我们采用蛋白质组学方法,比较未经顺铂处理和对顺铂耐药的膀胱癌细胞系中差异调节的蛋白质表达谱,以筛选与顺铂耐药相关的候选分子。通过将T24细胞逐步暴露于高达40μM的顺铂,建立了顺铂耐药细胞系T24。我们通过琼脂糖二维凝胶电泳,随后进行液相色谱串联质谱分析,对膀胱癌细胞系中的蛋白质表达进行了全面研究,这些细胞系包括未经顺铂处理的(T24)和顺铂耐药的细胞(T24CDDPR)。我们鉴定出T24和T24 CDDPR中有25个明显不同的斑点。与T24相比,T24CDDPR中有7个斑点表达增加,18个斑点表达减少。细胞骨架蛋白和酶调节剂在差异蛋白中最为突出。在这25种蛋白质中,我们选择了HNRNPA3、PCK2、PPL、PGK1、TKT、SERPINB2、GOT2和EIF3A通过蛋白质免疫印迹进行进一步验证。与T24相比,HNRNPA3、PGK1、TKT和SERPINB2在T24CDDPR中的表达增加了1.5倍以上。与T24相比,PCK2和PPL在T24CDDPR中的表达下降不到20%。本研究中25种新蛋白质的结果可能具有重要价值,并可能导致新分子标志物的开发。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验