S100A4 regulates E-cadherin expression in oral squamous cell carcinoma

被引:49
作者
Moriyama-Kita, M
Endo, Y
Yonemura, Y
Heizmann, CW
Miyamori, H
Sato, H
Yamamoto, E
Sasaki, T
机构
[1] Kanazawa Univ, Grad Sch Med, Dept Oral & Maxillofacial Surg, Kanazawa, Ishikawa 9208640, Japan
[2] Kanazawa Univ, Dept Expt Therapeut, Kanazawa, Ishikawa 9200934, Japan
[3] Kanazawa Univ, Dev Ctr Mol Target Drugs, Inst Canc Res, Kanazawa, Ishikawa 9200934, Japan
[4] Shizuoka Canc Ctr, Dept Gastr Canc, Shizuoka 4110934, Japan
[5] Univ Zurich, Dept Pediat, Div Clin Chem & Biochem, CH-8032 Zurich, Switzerland
[6] Kanazawa Univ, Inst Canc Res, Dept Mol Oncol & Virol, Kanazawa, Ishikawa 9200934, Japan
关键词
S100A4; E-cadherin; oral cancer;
D O I
10.1016/j.canlet.2004.12.046
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
S100A4 has multiple functions in cell cycle progression and cell motility, and has been implicated in cancer invasion. In this study, we examined the expression of S100A4, E-cadherin and its related proteins in oral squamous cell carcinoma (SCC) cell lines with different invasive phenotypes, grade 4C and 4D. Furthermore, grade 4C OSC-19 cells expressing E-cadherin were transfected with S100A4-expression vector and the expression of E-cadherin-related proteins in the stable clone was examined to elucidate the relationship between S100A4 and E-cadherin. Constitutive over-expression of S100A4 in stable transformant of OSC-19 (OSC-19/S100A4) cells led to down-regulation of E-cadherin and beta-catenin. Furthermore, grade 4D invasive cell lines (HOC313 and TSU) expressing S100A4 mRNA did not express E-cadherin, P-cadherin, and beta-catenin, while gamma-catenin protein was only weakly expressed. Thus, the mRNA expression of E-cadherin was reversely correlated with S100A4 expression in oral SCCs. Interestingly, vascular endothelial growth factor-C was up-regulated in OSC-19/S100A4 cells. In summary, S100A4-mediated regulation of E-cadherin expression may play an important mechanism in invasion and metastasis of oral SCC. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:211 / 218
页数:8
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