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蛋白质组学检测结直肠腺瘤及早期恶变患者血清的差异蛋白质变化及意义
引用本文:吴晓滨,彭俊生,李初俊,王辉,杜艳平,杨祖立,向军,胡坤华,刘炜,黎明涛. 蛋白质组学检测结直肠腺瘤及早期恶变患者血清的差异蛋白质变化及意义[J]. 中国病理生理杂志, 2009, 24(6): 1098-1103. DOI: 1000-4718
作者姓名:吴晓滨  彭俊生  李初俊  王辉  杜艳平  杨祖立  向军  胡坤华  刘炜  黎明涛
作者单位:中山大学附属第六医院 1食管胃肠外科, 2消化内科, 3结直肠肛门外科,4中山大学蛋白质组学研究中心, 广东 广州 510655
摘    要:目的: 通过比较分析结直肠腺瘤及早期恶变患者血清蛋白质的表达差异,寻找结直肠癌早期诊断的血清标记物。方法:建立结直肠腺瘤及腺瘤早期恶变患者血清蛋白双向电泳图谱,比较分析差异蛋白质斑点,切取酶解行MALDI-TOF/TOF质谱分析鉴定。结果:成功建立结直肠腺瘤及早期恶变患者血清蛋白双向电泳图谱,其平均蛋白质点分别为1672±73和1732±46,早期恶变组表达差异大于1.5倍的蛋白质斑点有28个,其中15个下调,13个上升;质谱分析鉴定出23个蛋白质,鉴定率达82.14%;合并重复鉴定的蛋白质,共获得的差异蛋白13种,其中8种为上调蛋白,5种为下调蛋白,分为6类,包括蛋白酶抑制剂、补体系统、免疫球蛋白、角质素、信号转导蛋白及未知蛋白。结论:蛋白质组学技术能灵敏分析结直肠腺瘤及早期恶变患者血清蛋白质的异常改变,本研究鉴定的蛋白质可能成为结直肠癌早期诊断的血清肿瘤标记物。

关 键 词:结直肠腺瘤  结直肠腺癌  
收稿时间:2008-12-25
修稿时间:2009-04-21

Identification of serum differential proteins in colorectal adenoma and early malignantly transformed adenoma by proteomics
WU Xiao-bin,PENG Jun-sheng,LI Chu-jun,WANG Hui,DU Yan-ping,YANG Zu-li,XIANG Jun,HU Kun-hua,LIU Wei,LI Ming-tao. Identification of serum differential proteins in colorectal adenoma and early malignantly transformed adenoma by proteomics[J]. Chinese Journal of Pathophysiology, 2009, 24(6): 1098-1103. DOI: 1000-4718
Authors:WU Xiao-bin  PENG Jun-sheng  LI Chu-jun  WANG Hui  DU Yan-ping  YANG Zu-li  XIANG Jun  HU Kun-hua  LIU Wei  LI Ming-tao
Affiliation:1Department of Gastrointestinal Surgery; 2Department of Gastroenterology; 3Department of Colorectal Surgery, The Sixth Affiliated Hospital of Sun Yat-sen University; 4Institute of Proteomics, SUN Yat-sen University, Guangzhou 510655, China. E-mail: pengjunsheng@tom.com
Abstract:AIM: To investigate the associated proteins and sensitive biomarkers for early diagnosis of colorectal adenocarcinoma by comparing the results of differential proteomic analysis between colorectal adenoma and early malignantly transformed adenoma. METHODS: Two-dimensional gel electrophoresis was used to define patterns of protein expressions of colorectal adenoma and early malignantly transformed adenoma. Proteins expressed differentially among groups were detected, cut out and analyzed by MALDI-TOF/TOF mass spectrometry. RESULTS: Two-dimensional protein maps of colorectal adenoma and early malignantly transformed adenoma were analyzed with gel-analysis software, an average of 1 672 spots in adenoma, 1 732 in early malignantly transformed adenoma were observed. 28 spots of a 1.5-fold change were found, including 15 proteins down-regulated and 13 up-regulated in early malignantly transformed adenoma, in which 23 proteins were identified by mass spectrometry, the rate of identification was 82.14%. 13 differential proteins were attained, 8 were up-regulated and 5 were down-regulated, which was classified to 6 categories, including protease inhibitor, complement, immunoglobulin, keratoproteins, signal transduction protein and function-unknown proteins. CONCLUSION: The changes of serum proteins in early malignantly transformed adenoma from adenoma can be identified by proteomic technology. Proteins detected in the study may provide new biomarkers correlated with biological behavior of colorectal adenocarcinoma.
Keywords:Colorectal adenoma  Colorectal adenocarcinoma  Proteomic
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