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LCM纯化的鼻咽癌间质和正常鼻咽间质的定量蛋白质组学研究
引用本文:李美香,肖志强,彭芳,李国庆,张鹏飞,李茂玉,李萃,李锋,刘迎福,陈主初.LCM纯化的鼻咽癌间质和正常鼻咽间质的定量蛋白质组学研究[J].生物化学与生物物理进展,2009,36(9):1122-1133.
作者姓名:李美香  肖志强  彭芳  李国庆  张鹏飞  李茂玉  李萃  李锋  刘迎福  陈主初
作者单位:1. 中南大学湘雅医院卫生部肿瘤蛋白质组学重点实验室,长沙,410008;中南大学湘雅医学院肿瘤研究所,长沙,410078;南华大学医学院组织胚胎学教研室,衡阳,421001
2. 中南大学湘雅医院卫生部肿瘤蛋白质组学重点实验室,长沙,410008
3. 中南大学湘雅医院卫生部肿瘤蛋白质组学重点实验室,长沙,410008;南华大学生命科学与技术学院,衡阳,421001
4. 中南大学湘雅医学院肿瘤研究所,长沙,410078
5. 中南大学湘雅医院卫生部肿瘤蛋白质组学重点实验室,长沙,410008;中南大学湘雅医学院肿瘤研究所,长沙,410078
基金项目:国家重点基础研究发展规划(973)(2001cb510207), 教育部跨世纪优秀人才培养计划基金(教计函[2002]48), 湖南省科技厅重大科技专项(06SK2004), 国家自然科学基金(30500558, 30800419)和教育部新世纪优秀人才培养计划基金(教育部科技函[2007]70)资助项目
摘    要:间质在肿瘤发生发展中的作用越来越受到重视.为寻找与鼻咽癌( nasopharyngeal carcinoma,NPC )发生发展相关的特异性间质蛋白,采用激光捕获显微切割技术( laser capture microdissection,LCM )纯化鼻咽癌间质和正常鼻咽黏膜间质,荧光差异双向凝胶电泳( fluorescent two-dimensional difference gel electrophoresis 2-D,DIGE )结合质谱技术分离鉴定间质相关蛋白.Western blot及免疫组织化学技术验证了其中3个差异蛋白(CapG、L-plastin和S100A9),证实了2D-DIGE结果的可靠性.建立了LCM 纯化的鼻咽癌间质和正常鼻咽间质的荧光差异蛋白表达图谱,高通量筛选与肿瘤发生相关的间质蛋白,共得到34个有统计学意义的蛋白质点,质谱鉴定得到20个差异蛋白.研究结果提示:这些差异表达的蛋白质将有助于阐明鼻咽癌细胞和周围间质的关系.对间质蛋白功能的进一步研究,将有助于解析间质在肿瘤发生中的作用机制,并为从间质途径寻找肿瘤治疗靶标提供新思路.

关 键 词:鼻咽癌,间质,激光捕获显微切割,荧光差异双向凝胶电泳,质谱,Western  blot,免疫组织化学
收稿时间:2009/1/30 0:00:00
修稿时间:2009/3/13 0:00:00

Quantitative Proteomics Analysis of LCM Purified Stroma of Nasopharyngeal Carcinoma and Normal Nasopharyngeal Mucosa
LI Mei-Xiang,XIAO Zhi-Qiang,PENG Fang,LI Guo-Qing,ZHANG Peng-Fei,LI Mao-Yu,LI Cui,LI Feng,LIU Ying-Fu and CHEN Zhu-Chu.Quantitative Proteomics Analysis of LCM Purified Stroma of Nasopharyngeal Carcinoma and Normal Nasopharyngeal Mucosa[J].Progress In Biochemistry and Biophysics,2009,36(9):1122-1133.
Authors:LI Mei-Xiang  XIAO Zhi-Qiang  PENG Fang  LI Guo-Qing  ZHANG Peng-Fei  LI Mao-Yu  LI Cui  LI Feng  LIU Ying-Fu and CHEN Zhu-Chu
Institution:Key Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University, Changsha 410008, China;Cancer Research Institute, Xiangya School of Medicine, Central South University, Changsha 410078, China;Department of Histology and Embryology, University of South China, Hengyang 421001, China;Key Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University, Changsha 410008, China;Key Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University, Changsha 410008, China;Key Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University, Changsha 410008, China;School of Life Science and Technology, University of South China, Hengyang 421001, China;Key Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University, Changsha 410008, China;Key Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University, Changsha 410008, China;Key Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University, Changsha 410008, China;Cancer Research Institute, Xiangya School of Medicine, Central South University, Changsha 410078, China;Key Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University, Changsha 410008, China;Cancer Research Institute, Xiangya School of Medicine, Central South University, Changsha 410078, China;Key Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University, Changsha 410008, China
Abstract:The mechanism of how stroma plays an important role in tumor carcinogenesis is now a hotspot. To delineate the features of stromal protein between nasopharyngeal carcinoma (NPC) and normal nasopharyngeal mucosa(NNM), laser capture microdissection (LCM) was performed to purify stromal cells from the NPC and NNM, respectively. The protein expressed profiles of the stroma of NPC and NNM were compared using fluorescent two-dimensional difference gel electrophoresis (2D-DIGE) and 34 differential protein spots between tumor stroma and normal stroma were chosen to be identified by mass spectrometry (MS). A total of 20 differential proteins were identified, and three differential proteins (CapG, L-plastin and S100A9) were selectively further validated by Western blotting and immunohistochemical analysis to confirm the results of 2D-DIGE. 2D-DIGE patterns of the stroma of NPC and NNM were established for the first time, the results suggested that differentially expressed proteins in the stroma of NPC and NNM may be useful for understanding the relationship between NPC cells and their surrounding microenvironment. Further studying of these proteins will be helpful to elucidate the mechanisms of NPC carcinogenesis and provide new thoughts on therapy of NPC through stroma.
Keywords:nasopharyngeal carcinoma  stroma  laser capture microdissection  two-dimensional fluorescence difference gel electrophoresis (2-D DIGE)  mass spectrum(MS)  Western blot  immunohistochemistry
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