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Head Neck ; 33(10): 1458-66, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21928418

ABSTRACT

BACKGROUND: We evaluated the predictive significance of 14 reported markers using immunohistochemical study in nasopharyngeal carcinoma. METHODS: Immunohistochemical stainings were done in 38 patients for Met, cyclooxygenase-2 (COX-2), nm23-H1, epidermal growth factor receptor (EGFR), p63, early growth response factor 1 (Egr1), chromosome segregation 1-like (CSE1L), cathepsin-D (aspartyl protease), C-erbB2, p53, signal transducers and activators of transcription (STAT3/STAT5), CD138 (Syndecan-1), and LIN28 with the usual methods. RESULTS: The median follow-up time was 30 months (11-83 months). High Met and CD138 expression were statistically significant negative prognostic factors on survival. The expression of Egr1 had a positive prognostic effect on survival. The combined score of these 3 markers, Met plus CD138 minus Egr1, was a strong prognostic factor. The median survival curve was distinctly separated in accord with this combined score. No prognostic value was revealed in COX-2, nm23-H1, EGFR, p63, CSE1L, cathepsin-D, C-erbB2, p53, STAT3, STAT5, and LIN28. CONCLUSIONS: The combined score of these markers could be used to stratify biomolecular risk groups.


Subject(s)
Biomarkers, Tumor/metabolism , Nasopharyngeal Neoplasms/metabolism , Nasopharyngeal Neoplasms/mortality , Adult , Aged , Carcinoma/metabolism , Carcinoma/mortality , Carcinoma/therapy , Cathepsin D/metabolism , Cellular Apoptosis Susceptibility Protein/metabolism , Chemotherapy, Adjuvant , Cyclooxygenase 2/metabolism , Disease-Free Survival , Early Growth Response Protein 1/metabolism , ErbB Receptors/metabolism , Female , Follow-Up Studies , Humans , Immunohistochemistry , Male , Middle Aged , NM23 Nucleoside Diphosphate Kinases/metabolism , Nasopharyngeal Neoplasms/therapy , Prognosis , Proto-Oncogene Proteins c-met/metabolism , RNA-Binding Proteins/metabolism , Radiotherapy, Intensity-Modulated , Receptor, ErbB-2/metabolism , STAT3 Transcription Factor/metabolism , STAT5 Transcription Factor/metabolism , Syndecan-1/metabolism , Transcription Factors/metabolism , Tumor Suppressor Protein p53/metabolism , Tumor Suppressor Proteins/metabolism
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