TY - JOUR
T1 - Proteomic analysis of global alteration of protein expression in squamous cell carcinoma of the esophagus
AU - Zhou, Ge
AU - Li, Hongmei
AU - Gong, Yi
AU - Zhao, Yingxin
AU - Cheng, Jingke
AU - Lee, Peng
AU - Zhao, Yingming
PY - 2005/9
Y1 - 2005/9
N2 - Squamous cell carcinoma of the esophagus (ESCC), a major subtype of esophageal carcinoma, is one of the aggressive cancers with worst prognosis in the world. The dismal outcome of ESCC is attributed to multiple reasons including its aggressive nature, largely unknown molecular mechanism of its progression, and the lack of biomarkers for early detection and effective prediction of its clinical behavior. To identify proteins with prognostic and/or predictive value, we applied a proteomics strategy to quantify proteins differentially expressed in ESCC using matched samples of carcinoma and adjacent normal epithelial cells. The analysis led to identification of 28 proteins aberrantly expressed in cancer cells with changes of at least three-fold in ESCC relative to normal squamous epithelial cells. These changes represent functional alterations of essential proteins for normal cellular physiology, accounting for many cellular changes involved in development of ESCC, including cell transformation, loss of differentiation, tumor growth, apoptosis, tumor invasion, and cell metabolism. The differentially expressed proteins shed new insights on the mechanism of tumorigenesis and provide candidate biomarkers for early detection of ESCC.
AB - Squamous cell carcinoma of the esophagus (ESCC), a major subtype of esophageal carcinoma, is one of the aggressive cancers with worst prognosis in the world. The dismal outcome of ESCC is attributed to multiple reasons including its aggressive nature, largely unknown molecular mechanism of its progression, and the lack of biomarkers for early detection and effective prediction of its clinical behavior. To identify proteins with prognostic and/or predictive value, we applied a proteomics strategy to quantify proteins differentially expressed in ESCC using matched samples of carcinoma and adjacent normal epithelial cells. The analysis led to identification of 28 proteins aberrantly expressed in cancer cells with changes of at least three-fold in ESCC relative to normal squamous epithelial cells. These changes represent functional alterations of essential proteins for normal cellular physiology, accounting for many cellular changes involved in development of ESCC, including cell transformation, loss of differentiation, tumor growth, apoptosis, tumor invasion, and cell metabolism. The differentially expressed proteins shed new insights on the mechanism of tumorigenesis and provide candidate biomarkers for early detection of ESCC.
KW - Cancer-specific protein marker
KW - Esophageal squamous cell carcinoma
UR - http://www.scopus.com/inward/record.url?scp=25844517518&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=25844517518&partnerID=8YFLogxK
U2 - 10.1002/pmic.200401230
DO - 10.1002/pmic.200401230
M3 - Article
C2 - 16127732
AN - SCOPUS:25844517518
SN - 1615-9853
VL - 5
SP - 3814
EP - 3821
JO - Proteomics
JF - Proteomics
IS - 14
ER -