Discovery of stage-related proteins in esophageal squamous cell carcinoma using proteomic analysis

被引:4
|
作者
Liu, Dong-Ping
Qi, Robert Z.
Wang, Yan
Chen, Ping-Ping
Koeffler, H. Phillip
Xie, Dong
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, Mol Oncol Lab, Inst Nutr Sci ,Grad Sch, Shanghai 200031, Peoples R China
[2] Hong Kong Univ Sci & Technol, Dept Biochem, Hong Kong, Hong Kong, Peoples R China
[3] Zhengzhou Univ, Coll Publ Hlth, Zhengzhou, Peoples R China
[4] Univ Calif Los Angeles, Sch Med, Cedars Sinai Med Ctr, Dept Hematol & Oncol, Los Angeles, CA 90024 USA
关键词
esophageal squamous cell carcinoma; TNM stage; two-dimensional gel electrophoresis;
D O I
10.1002/prca.200600815
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Esophageal squamous cell carcinoma (ESCC) is the major subtype of esophageal cancers in China,. and characterized with high morbidity and mortality. So far, the diagnosis of ESCC is mainly dependent on the alterations in esophageal histology, but most cases of ESCC with low stage do not display visible histological abnormalities. Therefore, a deep understanding of the mechanism of ESCC progression and seeking stage-specific molecules might improve the diagnosis and therapy for ESCC. In this study, we used proteomics to analyze ESCC tissues with classification by TNM stage, and determined the proteomic features correlated with ESCC progression (from stages I to III). Proteins that exhibited significantly different expression patterns between ESCC and corresponding normal esophageal tissues were identified using MS. The identified proteins with differentiated expression mainly fen into three protein categories (i.e. cytoskeleton system-associated proteins, metabolism enzymes, and heat shock proteins). In addition, real-time PCR highlighted some molecules that were associated with tumor stages at the mRNA level, such as enolase 1, chromosome 1 ORF 10, elastase inhibitor, cc B crystalline, stress-induced phosphoprotein 1, and squamous cell carcinoma antigen 1. Altogether, these data provided further information on ESCC progression and potential drug targets for ESCC clinical therapy.
引用
收藏
页码:312 / 320
页数:9
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