Original Article
Modern Pathology advance online publication 13 November 2009; doi: 10.1038/modpathol.2009.160
Upregulation of vimentin and aberrant expression of E-cadherin/
-catenin complex in oral squamous cell carcinomas: correlation with the clinicopathological features and patient outcome
Lai-Kui Liu1,2, Xiao-Yun Jiang2,3, Xiang-Xiang Zhou2, Dong-Miao Wang2,3, Xiao-Ling Song1 and Hong-Bing Jiang2,3
- 1Department of Oral Pathology, College of Stomatology, Nanjing Medical University, Jiangsu, China
- 2Department of Oral Pathology, Institute of Stomatology, Nanjing Medical University, Jiangsu, China
- 3Department of Oral and Maxillofacial Surgery, College of Stomatology, Nanjing Medical University, Jiangsu, China
Correspondence: Dr L-K Liu, Department of Oral Pathology, College of Stomatology, Nanjing Medical University, 136# Hanzhong Road, Nanjing, Jiangsu 210029, China. E-mail: laikuiliu@sina.com; Dr H-B Jiang, Department of Oral and Maxillofacial Surgery, College of Stomatology, Nanjing Medical University, 136# Hanzhong Road, Nanjing, Jiangsu 210029, China. E-mail: jhbcd@sina.com
Received 29 June 2009; Revised 8 October 2009; Accepted 11 October 2009; Published online 13 November 2009.
Abstract
Oral squamous cell carcinoma is a challenging oncology problem. A reliable biomarker for metastasis or high-risk prognosis in oral cancer patients remains undefined. Using quantitative immunohistochemistry, we examined the expression of vimentin, E-cadherin, and
-catenin in 83 oral squamous cell carcinoma patients, and the relationships between the expression of these markers and specific clinicopathological features were analysed. The high expression of vimentin was observed in 23 of 43 (53%) tumours from patients who eventually developed a recurrent tumour and was associated with recurrence and death (P<0.001 and <0.001, respectively). The decreased expression of E-cadherin was observed in 36 of 43 (84%) tumours from patients who eventually developed a recurrent tumour and was also associated with recurrence and death (P<0.001 and <0.001, respectively). Although no correlation between
-catenin expression in whole-tumour sections and clinicopathological features was observed, decreased
-catenin expression at the tumour invasive front was closely associated with recurrence and death (P=0.002 and 0.002, respectively). The expression of vimentin and that of E-cadherin were associated with survival and were independent prognostic factors in univariate and multivariate analyses. Our data show that the overexpression of vimentin was closely associated with recurrence and death in oral squamous cell carcinoma patients. The combination of the upregulation of vimentin and aberrant expression of E-cadherin/
-catenin complexes at the tumour invasive front may provide a useful prognostic marker in oral squamous cell carcinoma.
Keywords:
vimentin, oral squamous cell carcinoma, immunohistochemistry

