Volume 29, Issue 1 470314 pp. 21-29
Article
Open Access

14-3-3 Sigma And p53 Expression in Gastric Cancer and Its Clinical Applications

Gilbert Mühlmann

Corresponding Author

Gilbert Mühlmann

Center of Operative Medicine Department of Visceral Transplant and Thoracic Surgery Innsbruck Medical University, Austria , i-med.ac.at

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Dietmar Öfner

Dietmar Öfner

Department of Surgery Paracelsus Private Medical University Salzburger Landeskliniken Salzburg, Austria , pmu.ac.at

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Matthias Zitt

Matthias Zitt

Center of Operative Medicine Department of Visceral Transplant and Thoracic Surgery Innsbruck Medical University, Austria , i-med.ac.at

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Hannes M. Müller

Hannes M. Müller

Center of Operative Medicine Department of Visceral Transplant and Thoracic Surgery Innsbruck Medical University, Austria , i-med.ac.at

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Hans Maier

Hans Maier

Department of Pathology Innsbruck Medical University, Austria , i-med.ac.at

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Patrizia Moser

Patrizia Moser

Department of Pathology Innsbruck Medical University, Austria , i-med.ac.at

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Kurt W. Schmid

Kurt W. Schmid

Institute of Pathology and Neuropathology University Hospital Essen, Germany , uk-essen.de

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Marion Zitt

Marion Zitt

Center of Operative Medicine Department of Visceral Transplant and Thoracic Surgery Innsbruck Medical University, Austria , i-med.ac.at

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Albert Amberger

Albert Amberger

Tyrolean Cancer Research Institute Innsbruck, Austria , tcri.at

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First published: 29 May 2013
Citations: 2

Abstract

14-3-3 sigma (σ) induces G2 arrest enabling the repair of damaged DNA. The function of 14-3-3 σ is frequently lost in tumor cells, indicating a potential tumor suppressor function. The purpose of this study was to evaluate the prognostic value of 14-3-3 σ expression in human gastric cancer. 14-3-3 σ expression was analyzed by immunohistochemistry in 157 tumor samples of patients, who underwent resection for gastric cancer. Since 14-3-3 σ is involved in the p53 network, p53 expression was detected in parallel and correlated with 14-3-3 σ. 14-3-3 σ was found to be overexpressed in 75 (47.8%) of 157 cases, the overexpression rate of p53 protein was 27.4%. 14-3-3 σ overexpression was statistically significantly associated with pT-stage (p=0.041) pN-stage (p=0.015) and UICC-stage (p=0.019) and showed a borderline significance with Lauren classification (p=0.057). Univariate survival calculations revealed a coexistent 14-3-3 σ and p53 overexpression as a significant predictor of disease-free survival. Multivariate analysis did not unfold 14-3-3 as an independent prognostic factor for disease-free survival and overall survival. Concomitant 14-3-3 σ and p53 overexpression in tumor cells of patients with gastric cancer identifies a population of patients with relatively unfavorable prognosis.

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