## Abstract Suppression subtractive hybridization (SSH) was performed for isolation of tissueโspecific genes in nasopharyngeal epithelial tissue, by use of cDNAs from human adult nasopharyngeal epithelial tissue as tester and mixed cDNAs from esophagus, lung, liver, heart, stomach, spleen, skeletal
Quantitative proteomic analysis of differential proteins in the stroma of nasopharyngeal carcinoma and normal nasopharyngeal epithelial tissue
โ Scribed by Mei-Xiang Li; Zhi-Qiang Xiao; Ying-Fu Liu; Yong-Heng Chen; Cui Li; Peng-Fei Zhang; Mao-Yu Li; Feng Li; Fang Peng; Chao-Jun Duan; Hong Yi; Hui-Xin Yao; Zhu-Chu Chen
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 391 KB
- Volume
- 106
- Category
- Article
- ISSN
- 0730-2312
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โฆ Synopsis
Abstract
The importance of stromal cells and the factors that they expressed during cancer initiation and progression have been highlighted by recent literature. To identify the stromal proteins involved in nasopharyngeal carcinoma (NPC) carcinogenesis, we assessed differences in protein expression of the stroma from NPC and normal nasopharyngeal epithelium tissues (NNET) using a quantitative proteomic approach combined with laser capture microdissection (LCM). LCM was performed to purify stromal cells from the NPC and NNET, respectively. The differential proteins between the pooled microdissected tumor and normal stroma were analyzed by twoโdimensional difference gel electrophoresis (2DโDIGE) combined with mass spectrometry (MS). Twenty differential proteins were identified, and the expression and location of two differential proteins (Lโplastin and S100A9) were further confirmed by Western blotting and immunohistochemical analysis. Our results will be helpful to study the role of stroma in the NPC carcinogenesis, as well as discover the interaction between NPC cells and their surrounding microenvironment. J. Cell. Biochem. 106: 570โ579, 2009. ยฉ 2009 WileyโLiss, Inc.
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