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Oncol Rep ; 24(4): 949-55, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20811675

ABSTRACT

In this study, we investigated the expression of 14-3-3sigma tumor suppressor gene in a panel of NPC cell lines, xenografts and primary tumors. Our objective was to determine the correlation between 14-3-3sigma expression and clinical outcome in NPC. We detected reduced 14-3-3sigma expression in 5/6 NPC tumor lines by quantitative RT-PCR and Western blotting. By immunohistochemical staining, significant down-regulation of 14-3-3sigma was also found in 26/72 (36.1%) primary tumors of NPC patients, who were treated with curative radiotherapy. Promoter methylation was confirmed in a subset of primary tumors by methylation-specific PCR analysis. Importantly, we demonstrated that 14-3-3sigma expression is significantly associated with both overall survival (OS) and cancer-specific survival (CSS), but not with the clinical staging of NPC patients. The low 14-3-3sigma expression was associated with improved overall (p=0.029) and cancer-specific survival (p=0.042) on univariate analysis. 14-3-3sigma expression and staging were also independent variables to all the prognostic factors under multivariate analysis. In conclusion, low expression of 14-3-3sigma appears to be a valuable marker for better survival in patient with NPC. These results provide the evidence that 14-3-3sigma expression is a significant prognostic factor for NPC patients.


Subject(s)
14-3-3 Proteins/biosynthesis , Biomarkers, Tumor/analysis , Carcinoma/metabolism , Exonucleases/biosynthesis , Adult , Aged , Aged, 80 and over , Animals , Biomarkers, Tumor/biosynthesis , Blotting, Western , Carcinoma/mortality , Carcinoma/pathology , DNA Methylation , Exoribonucleases , Female , Gene Expression , Humans , Immunohistochemistry , Kaplan-Meier Estimate , Male , Middle Aged , Nasopharyngeal Carcinoma , Nasopharyngeal Neoplasms/metabolism , Nasopharyngeal Neoplasms/mortality , Nasopharyngeal Neoplasms/pathology , Neoplasm Staging , Prognosis , Promoter Regions, Genetic/genetics , Reverse Transcriptase Polymerase Chain Reaction , Xenograft Model Antitumor Assays , Young Adult
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