Direct analysis of laser capture microdissected endometrial carcinoma and epithelium by matrix-assisted laser desorption/ionization mass spectrometry

被引:23
作者
Guo, JZ
Colgan, TJ
DeSouza, LV
Rodrigues, MJ
Romaschin, AD
Siu, KWM
机构
[1] York Univ, Dept Chem, Toronto, ON M3J 1P3, Canada
[2] York Univ, Ctr Res Mass Spectrometry, Toronto, ON M3J 1P3, Canada
[3] Mt Sinai Hosp, Toronto, ON M5G 1X5, Canada
[4] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON M5G 1L5, Canada
[5] Toronto Gen Hosp, Toronto, ON M5G 2C4, Canada
关键词
D O I
10.1002/rcm.2119
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Direct analysis of laser capture microdissected malignant and normal endometrial epithelium using matrix-assisted laser desorption/ionization (MALDI) time-of-flight mass spectrometry (MS) was able to detect a number of proteins that are overexpressed in malignant epithelial cells. A total of 16 physiologic and malignant endometrial samples were laser capture microdissected, including four proliferative and four secretory endometria, and eight endometrioid adenocarcinomas. Two of these proteins, at 10 834 and 10 843 Da, likely correspond to calgranulin A and chaperonin 10, two proteins that had previously been identified in endometrioid adenocarcinoma in whole tissue homogenate by MS analysis. Direct analysis by MALDI-MS not only confirms that these proteins are overexpressed in endometrial carcinoma, but also localizes them to the epithelial cells, the expected cancer site. Copyright (C) 2005 John Wiley & Sons, Ltd.
引用
收藏
页码:2762 / 2766
页数:5
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