Registro completo |
Provedor de dados: |
BJMBR
|
País: |
Brazil
|
Título: |
MMP-1/PAR-1 signal transduction axis and its prognostic impact in esophageal squamous cell carcinoma
|
Autores: |
Peng,Hong-hua
Zhang,Xi
Cao,Pei-guo
|
Data: |
2012-01-01
|
Ano: |
2012
|
Palavras-chave: |
Matrix metalloprotease-1
Protease-activated receptor-1
Esophageal squamous cell carcinoma
Prognosis
Immunohistochemistry
|
Resumo: |
The matrix metalloprotease-1 (MMP-1)/protease-activated receptor-1 (PAR-1) signal transduction axis plays an important role in tumorigenesis. To explore the expression and prognostic value of MMP-1 and PAR-1 in esophageal squamous cell carcinoma (ESCC), we evaluated the expression of two proteins in resected specimens from 85 patients with ESCC by immunohistochemistry. Sixty-two (72.9%) and 58 (68.2%) tumors were MMP-1- and PAR-1-positive, respectively, while no significant staining was observed in normal esophageal squamous epithelium. MMP-1 and PAR-1 overexpression was significantly associated with tumor node metastasis (TNM) stage and regional lymph node involvement. Patients with MMP-1- and PAR-1-positive tumors, respectively, had poorer disease-free survival (DFS) than those with negative ESCC (P = 0.002 and 0.003, respectively). Univariate analysis showed a significant relationship between TNM stage [hazard ratio (HR) = 2.836, 95% confidence interval (CI) = 1.866-4.308], regional lymph node involvement (HR = 2.955, 95%CI = 1.713-5.068), MMP-1 expression (HR = 2.669, 95%CI = 1.229-6.127), and PAR-1 expression (HR = 1.762, 95%CI = 1.156-2.883) and DFS. Multivariate analysis including the above four parameters identified TNM stage (HR = 2.035, 95%CI = 1.167-3.681), MMP-1 expression (HR = 2.109, 95%CI = 1.293-3.279), and PAR-1 expression (HR = 1.967, 95%CI = 1.256-2.881) as independent and significant prognostic factors for DFS. Our data suggest for the first time that MMP-1 and PAR-1 were both overexpressed in ESCC and are novel predictors of poor patient prognosis after curative resection. The MMP-1/PAR-1 signal transduction axis might be a new therapeutic target for future therapies tailored against ESCC.
|
Tipo: |
Info:eu-repo/semantics/article
|
Idioma: |
Inglês
|
Identificador: |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2012000100014
|
Editor: |
Associação Brasileira de Divulgação Científica
|
Relação: |
10.1590/S0100-879X2011007500152
|
Formato: |
text/html
|
Fonte: |
Brazilian Journal of Medical and Biological Research v.45 n.1 2012
|
Direitos: |
info:eu-repo/semantics/openAccess
|
|