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Immunohistochemical analysis of colorectal cancer with gastric phenotype: claudin-18 is associated with poor prognosis.

Authors :
Matsuda M
Sentani K
Noguchi T
Hinoi T
Okajima M
Matsusaki K
Sakamoto N
Anami K
Naito Y
Oue N
Yasui W
Source :
Pathology international [Pathol Int] 2010 Oct; Vol. 60 (10), pp. 673-80. Date of Electronic Publication: 2010 Aug 17.
Publication Year :
2010

Abstract

Claudin-18 plays a key role in constructing tight junctions, and altered claudin-18 expression has been documented in various human malignancies; however, little is known about the biological significance of claudin-18 in colorectal cancer (CRC). The aim of this study is to investigate the significance of claudin-18 expression in CRC and its association with clinicopathological factors. We performed clinicopathological analysis of claudin-18 expression in a total of 569 CRCs by immunohistochemistry. Moreover, we investigated the association between claudin-18 and various markers including gastric/intestinal phenotype (MUC5AC, MUC6, MUC2 and CD10), CDX2, claudin-3, claudin-4, p53 and Ki-67. Claudin-18 expression was detected in 21 of the 569 CRCs (4%) and was seen exclusively on the cell membrane. Positive expression of claudin-18 showed a significant correlation with positive expression of MUC5AC (P < 0.0001) and negative expression of CDX2 (P= 0.0013). The prognosis of patients with positive claudin-18 expression was significantly poorer than in negative cases (P= 0.0106). Multivariate analysis revealed that T grade, M grade and claudin-18 expression were independent predictors of survival in patients with CRC. We revealed that claudin-18 expression correlates with poor survival in patients with CRC and is associated with the gastric phenotype.<br /> (© 2010 The Authors. Pathology International © 2010 Japanese Society of Pathology and Blackwell Publishing Asia Pty Ltd.)

Details

Language :
English
ISSN :
1440-1827
Volume :
60
Issue :
10
Database :
MEDLINE
Journal :
Pathology international
Publication Type :
Academic Journal
Accession number :
20846265
Full Text :
https://doi.org/10.1111/j.1440-1827.2010.02587.x