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Vimentin is a potential prognostic factor for tongue squamous cell carcinoma among five epithelial-mesenchymal transition-related proteins

Authors :
Chih-Wen Shu
Yao-Dung Hsieh
Huei-Cin Sie
Ting-Ying Fu
Liang-Ming Yen
Yaoh-Shiang Lin
Yun-Chung Lin
Yi-Min Wu
Pei-Feng Liu
Bor-Hwang Kang
Luo-Ping Ger
Ju-Hsin Sun
I-Chien Hsieh
Huei-Han Liou
Yu-Kai Tseng
Source :
PLoS ONE, Vol 12, Iss 6, p e0178581 (2017), PLoS ONE
Publication Year :
2017
Publisher :
Public Library of Science (PLoS), 2017.

Abstract

We aimed to investigate the association of the expression levels of five epithelial–mesenchymal transition (EMT)-related proteins (Snail, Twist, E-cadherin, N-cadherin, and Vimentin) with tumorigenesis, pathologic parameters and prognosis in tongue squamous cell carcinoma (TSCC) patients by immunohistochemistry of tissue microarray. The expression levels of Snail, E-cadherin, N-cadherin and Vimentin were significantly different between the tumor adjacent normal and tumor tissues. In tumor tissues, lower E-cadherin and higher N-cadherin levels were associated with a higher grade of cell differentiation, advanced stage of disease, and lymph node metastasis. However, higher Vimentin expression was associated with poor cell differentiation and lymph node metastasis. Patients with low E-cadherin expression had poor disease-specific survival (DSS). Conversely, positive N-cadherin and higher Vimentin expression levels were associated with poor DSS and disease-free survival. Notably, our multivariate Cox regression model indicated that high Vimentin expression was an adverse prognostic factor for DSS in TSCC patients, even after the adjustment for cell differentiation, pathological stage, and expression levels of Snail, Twist, E-cadherin, and N-cadherin. Snail, E-cadherin, N-cadherin, and Vimentin were associated with tumorigenesis and pathological outcomes. Among the five EMT-related proteins, Vimentin was a potential prognostic factor for TSCC patients.

Details

Language :
English
ISSN :
19326203
Volume :
12
Issue :
6
Database :
OpenAIRE
Journal :
PLoS ONE
Accession number :
edsair.doi.dedup.....ec3defcb90c807513858cb9499a631ea