Heterogeneous expression of claudin-4 in human colorectal cancer: Decreased claudin-4 expression at the invasive front correlates cancer invasion and metastasis

被引:60
作者
Ueda, Junya
Semba, Shuho
Chiba, Hideki
Sawada, Norimasa
Seo, Yasushi
Kasuga, Masato
Yokozaki, Hiroshi
机构
[1] Kobe Univ, Grad Sch Med, Div Surg Pathol, Dept Biomed Informat,Chuo Ku, Kobe, Hyogo 6500017, Japan
[2] Kobe Univ, Grad Sch Med, Div Diabet Digest & Kidney Dis, Dept Clin Mol Med, Kobe, Hyogo 6500017, Japan
[3] Sapporo Med Univ, Sch Med, Dept Pathol, Sapporo, Hokkaido, Japan
关键词
claudin-4; colorectal cancer; invasion; metastasis;
D O I
10.1159/000101049
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objective: Claudin-4 plays a key role in constructing the tight junction (TJ), and altered claudin-4 expression has been documented in various human malignancies; however, little is known about the biological significance of claudin-4 in colorectal cancers (CRCs). The aim of this study is to investigate the significance of claudin-4 expression in CRC and its association with clinicopathological factors. Methods: The levels of claudin-4 expression in a total of 129 CRCs and 44 metastatic tumors were examined by immunohistochemistry. A small interfering RNA (siRNA)-mediated claudin-4 knockdown examination was also conducted to assess the biological role(s) of claudin-4 in cultured cells. Results: Expression of claudin-4 at the intercellular membrane was well preserved at the surface of the tumor; however, decreased claudin-4 expression was detected in 57% of CRCs, particularly at the invasive front. Interestingly, decreased claudin-4 expression was detected in metastatic lesions of CRC. The siRNA-mediated claudin-4 knockdown in SW480 claudin-4-positive CRC cells upregulated cell motility, whereas no significant change was detected in cell proliferation. Conclusions: These observations suggested that disruption of claudin-4-mediated TJ construction enhances cancer cell invasion and metastasis in human CRC. Claudin-4 might be a good biomarker for diagnosing the risk of distant metastasis. Copyright (c) 2007 S. Karger AG, Basel.
引用
收藏
页码:32 / 41
页数:10
相关论文
共 58 条
[1]   Claudin-3 and claudin-4 expression in ovarian epithelial cells enhances invasion and is associated with increased matrix metalloproteinase-2 activity [J].
Agarwal, R ;
D'Souza, T ;
Morin, P .
CANCER RESEARCH, 2005, 65 (16) :7378-7385
[2]  
Anderson JM, 2001, NEWS PHYSIOL SCI, V16, P126
[3]   Differential expression of claudin-2 in normal human tissues and gastrointestinal carcinomas [J].
Aung, PP ;
Mitani, Y ;
Sanada, Y ;
Nakayama, H ;
Matsusaki, K ;
Yasui, W .
VIRCHOWS ARCHIV, 2006, 448 (04) :428-434
[4]   The tight junction protein ZO-1 and an interacting transcription factor regulate ErbB-2 expression [J].
Balda, MS ;
Matter, K .
EMBO JOURNAL, 2000, 19 (09) :2024-2033
[5]  
Behrens J, 1992, Semin Cell Biol, V3, P169
[6]  
BOIREAU S, CARCINOGENESIS
[7]  
CARROZZINE F, 2005, AM J PHYSIOL-CELL PH, V89, pC1002
[8]   Restoration of tight junction structure and barrier function by down-regulation of the mitogen-activated protein kinase pathway in Ras-transformed Madin-Darby canine kidney cells [J].
Chen, YH ;
Lu, Q ;
Schneeberger, EE ;
Goodenough, DA .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (03) :849-862
[9]   New signals from the invasive front [J].
Christofori, G .
NATURE, 2006, 441 (7092) :444-450
[10]   Control of cell polarity and chemotaxis by Akt/PKB and PI3 kinase through the regulation of PAKa [J].
Chung, CY ;
Potikyan, G ;
Firtel, RA .
MOLECULAR CELL, 2001, 7 (05) :937-947