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Expression profiles for 14-3-3 zeta and CCL20 in pancreatic cancer and chronic pancreatitis.
Klemm, Christoph; Dommisch, Henrik; Göke, Friederike; Kreppel, Matthias; Jepsen, Søren; Rolf, Fimmers; Dommisch, Klaus; Perner, Sven; Standop, Jens.
Affiliation
  • Klemm C; Department for Oral and Cranio-Maxillo and Facial Plastic Surgery, University of Cologne, Germany. Electronic address: christoph.klemm@uk-koeln.de.
  • Dommisch H; Department of Periodontology, Operative and Preventive Dentistry, University Hospital Bonn, Bonn, Germany; Department of Oral Health Sciences, University of Washington, Seattle, WA, USA.
  • Göke F; Department of Prostate Cancer Research, University Hospital of Bonn, Germany; Institute of Pathology, University Hospital of Bonn, Germany.
  • Kreppel M; Department for Oral and Cranio-Maxillo and Facial Plastic Surgery, University of Cologne, Germany; Department of Radiation Oncology, University of Cologne, Germany.
  • Jepsen S; Department of Periodontology, Operative and Preventive Dentistry, University Hospital Bonn, Bonn, Germany.
  • Rolf F; Institute of Medical Biometry, Informatics and Epidemiology, University of Bonn, Germany.
  • Dommisch K; Oncology Center, Helios Clinic Schwerin, Schwerin, Germany.
  • Perner S; Department of Prostate Cancer Research, University Hospital of Bonn, Germany; Institute of Pathology, University Hospital of Bonn, Germany.
  • Standop J; Center of Integrated Oncology (CIO) Cologne-Bonn, Germany; Department of Surgery, University of Bonn, Germany.
Pathol Res Pract ; 210(6): 335-41, 2014 Jun.
Article in En | MEDLINE | ID: mdl-24629487
ABSTRACT

BACKGROUND:

Pancreatic cancer (PCA) has a dismal prognosis because it is often diagnosed at an advanced stage. The overall survival rate is <5% after five years. Chronic pancreatitis (CP) is one of the most important risk factors for PCA. A major difficulty is to distinguish between CP and PCA at both clinical and morphologic level. The aim of this study was to assess the impact of the expression profiles for 14-3-3 zeta and CCL20 to histologically discriminate between PCA and CP.

METHODS:

In PCA (n=138) and CP (n=36) tissue samples, the expression of 14-3-3 zeta and CCL20 was examined by immunohistochemistry. Associations between expression profiles of 14-3-3 zeta and CCL20 expression in PCA, CP as well as MANT (matched adjacent normal tissue) (n=138) and clinicopathologic variables were analyzed.

RESULTS:

The expression of CCL20 and 14-3-3 zeta was significantly higher in PCA than in CP and MANT. For CP compared to MANT, no significant differences were observed for expression profiles of both 14-3-3 zeta and CCL20.

CONCLUSION:

CCL20 and 14-3-3 zeta are molecules that play a putative role during tumorgenesis in pancreas, and may therefore be new parameters for histological diagnosis and discrimination between PCA and CP.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancreatic Neoplasms / Biomarkers, Tumor / 14-3-3 Proteins / Pancreatitis, Chronic / Chemokine CCL20 Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Pathol Res Pract Year: 2014 Document type: Article Publication country: ALEMANHA / ALEMANIA / DE / DEUSTCHLAND / GERMANY

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancreatic Neoplasms / Biomarkers, Tumor / 14-3-3 Proteins / Pancreatitis, Chronic / Chemokine CCL20 Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Pathol Res Pract Year: 2014 Document type: Article Publication country: ALEMANHA / ALEMANIA / DE / DEUSTCHLAND / GERMANY