Article Text
Abstract
Objective To evaluate the expression of epithelial membrane protein-2 (EMP2) protein and its clinicopathological associations in patients with nasopharyngeal carcinoma.
Design Retrospective population-based cohort study.
Setting This study was based on a biobank in Chi-Mei Medical Center (Tainan, Taiwan) from 1993 to 2002.
Participants Biopsies of 124 consecutive nasopharyngeal carcinoma patients without initial distant metastasis and treated with consistent guidelines were assessed. Immunoexpressions of EMP2 were analysed and the outcomes were correlated with clinicopathological features and patient survivals.
Primary and secondary outcome measures Immunoexpressions of EMP2 were analyzed and the outcomes were correlated with clinicopathological features and patient survivals.
Results Loss of EMP2 expression (49.2%) was correlated with advanced primary tumour (p=0.044), nodal status (p=0.045) and the 7th American Joint Committee on Cancer stage (p=0.027). In multivariate analyses, loss of EMP2 expression emerged as an independent prognosticator for worse disease-specific survival (DSS; p=0.015) and local recurrence-free survival (LRFS; p=0.030), along with the American Joint Committee on Cancer stages III–IV (p=0.034, DSS; p=0.023, LRFS).
Conclusions Loss of EMP2 expression is common and associated with adverse prognosticators and might confer tumour aggressiveness through hampering its interaction with specific membrane protein(s) and hence the downstream signal transduction pathway(s).
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Supplementary materials
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Footnotes
To cite: Chen Y-H, Wu L-C, Wu W-R, et al. Loss of epithelial membrane protein-2 expression confers an independent prognosticator in nasopharyngeal carcinoma: a cohort study. BMJ Open 2012;2:e000900. doi:10.1136/bmjopen-2012-000900
Contributors Y-HC, L-CW, W-RW, H-JL, S-WL, C-YL, S-LC, N-HC, H-YH, C-FL, H-PH and Y-LS participated in the conception and design, acquisition, analysis and interpretation of data. C-FL and Y-LS drafted the article and all authors revised it critically for important intellectual content. All authors gave final approval of the version to be published.
Funding This work was supported by grants DOH99-TD-C-111-004 (Department of Health, Taiwan) to C-FL for tissue dissection and immunohistochemical analysis; CMFHR10119 (Chi-Mei Medical Center) to L-CW for case history analysis; 98-2311-B-110-001-MY3 (National Science Council, Taiwan) to Y-LS for target (EMP2) prioritisation.
Competing interests None.
Ethics approval Ethics approval was provide by the institutional review board (IRB100-09-003).
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement The original immunostaining and statistical data are available from the corresponding author at ylshiue{at}mail.nsysu.edu.tw.