Expression of E-cadherin and vimentin correlates with metastasis formation in head and neck squamous cell carcinoma patients

被引:170
|
作者
Nijkamp, Monique M. [1 ]
Span, Paul N. [1 ]
Hoogsteen, Ilse J. [1 ]
van der Kogel, Albert J. [1 ]
Kaanders, Johannes H. A. M. [1 ]
Bussink, Johan [1 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Radiat Oncol, Nijmegen, Netherlands
关键词
EMT; E-cadherin; Vimentin; Head and neck tumour; GROWTH-FACTOR RECEPTOR; EPITHELIAL-MESENCHYMAL TRANSITION; LIGAND-INDEPENDENT ACTIVATION; TUMOR PROGRESSION; PROTEIN-KINASE; CANCER CELLS; AKT; CETUXIMAB; PATHWAYS; SURVIVAL;
D O I
10.1016/j.radonc.2011.05.066
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: E-cadherin is a transmembrane glycoprotein, involved in cell-cell adhesion and epithelial-mesenchymal transition (EMT). Vimentin is highly expressed in mesenchymal cells and is positively correlated with increased metastasis. Here we set out to determine the expression of E-cadherin and vimentin in head and neck squamous cell carcinomas (HNSCC). Patients and methods: Twenty-six patients with primary stage II-IV HNSCC were included. E-cadherin and vimentin were visualised using immunohistochemistry, semi-automatically analysed for expression patterns and correlated with the clinical behaviour of these tumours. Results: A large variation in E-cadherin and vimentin expression was observed between tumours (median 17% range 0-51% respectively median 0% range 0-20%). Tumours with low E-cadherin expression showed a significantly higher incidence of metastasis formation compared to tumours with high expression (81% versus 19%, p = 0.004). Enhanced expression of vimentin was associated with a trend towards a higher metastatic risk (33% versus 77%) compared to tumours without expression of vimentin. All patients with low E-cadherin and high vimentin expression (an EMT-phenotype) developed distant metastases versus only 44% of the other patients (p = 0.008). Conclusion: Loss of E-cadherin and gain of vimentin may be associated with enhanced migration of tumour cells, leading to higher metastatic risk of HNSCC patients. (C) 2011 Elsevier Ireland Ltd. All rights reserved. Radiotherapy and Oncology 99 (2011) 344-348
引用
收藏
页码:344 / 348
页数:5
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