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Clinicopathologic Significance of Putative Stem Cell Marker, CD44 and CD133, in Human Gastric Carcinoma
Author(s) -
CHEN SHI,
HOU JINGHUI,
FENG XINGYU,
ZHANG XIAOSHI,
ZHOU ZHIWEI,
YUN JINGPING,
CHEN YINGBO,
CAI MUYAN
Publication year - 2013
Publication title -
journal of surgical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.201
H-Index - 111
eISSN - 1096-9098
pISSN - 0022-4790
DOI - 10.1002/jso.23337
Subject(s) - cd44 , medicine , gastric carcinoma , pathology , carcinoma , stem cell marker , stem cell , clinical significance , cancer stem cell , oncology , cancer , cell , biology , genetics
Background and Objectives CD44 and CD133 have been reported as putative stem cell markers. However, the clinicopathologic significance of CD44 and CD133 expression in patients with gastric carcinoma (GC) has not been clearly elucidated. Methods Immunohistochemistry (IHC) was performed to investigate the CD44 and CD133 expression in gastric carcinomas and normal mucosal tissues. Receiver operating characteristic (ROC) curve analysis, spearman's rank correlation, Kaplan–Meier plots, and Cox proportional hazards regression model were used to analyze the data. Results The highly expressed CD44 and CD133 were observed in 27/152 (17.7%) and 64/152 (42.1%) of GCs and in 4/60 (6.7%) and 15/60 (25.0%) normal gastric mucosal tissues, respectively ( P  < 0.05, Fisher's exact test). High expression of CD44 was significantly correlated with tumor poorer differentiation, presence of distant metastasis, advanced TNM stage, and tumor relapse; and high expression of CD133 was positively associated with tumor invasion depth, presence of distant metastasis and advanced TNM stage. More importantly, high‐expressed CD44 and CD133 were both associated with shorter survival as evidenced by univariate and multivariate analysis. Conclusions Our study introduces high expression of CD44 and CD133 as adverse independent prognostic factors in GC patients. The combined CD44 and CD133 expression may become a useful tool for identifying patients with different clinical outcomes. J. Surg. Oncol. 2013;107:799–806. © 2013 Wiley Periodicals, Inc.

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