Correlation of β-catenin, but not PIN1 and cyclin D1, overexpression with disease-free and overall survival in patients with cancer of the parotid gland

Head Neck. 2015 Jan;37(1):30-6. doi: 10.1002/hed.23546. Epub 2014 Feb 6.

Abstract

Background: Malignant tumors of the salivary glands comprise about 3% to 5% of all head and neck carcinomas. The purpose of our study was to find possible predictive and/or prognostic markers for parotid cancer.

Methods: A total of 46 tissue samples of carcinomas of the parotid gland were immunohistochemically stained for ß-catenin, cyclin D1, and PIN1. The factors were analyzed regarding their prognostic value for disease-free and overall survival.

Results: An overexpression of the cytoplasmatic ß-catenin was linked to a statistically significant worse outcome regarding disease-free (p = .0296) and overall survival (p = .0416). The 5-year overall survival was 83.9% in patients without and 0% in patients presenting with overexpression of cytoplasmatic ß-catenin. Additionally, Union Internationale Contre le Cancer (UICC) stage correlated with overall survival (p = .0306) and disease-free survival (DFS; p = .0473).

Conclusion: Multivariate analysis showed that overexpression of cytoplasmatic ß-catenin and the UICC stage are 2 independent prognostic markers for survival in patients with parotid cancer.

Keywords: Cyclin D1; PIN1; parotid cancer; salivary gland cancer; ß-catenin.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Carcinoma / metabolism*
  • Carcinoma / mortality
  • Carcinoma / pathology
  • Cyclin D1 / metabolism*
  • Disease-Free Survival
  • Female
  • Humans
  • Male
  • Middle Aged
  • NIMA-Interacting Peptidylprolyl Isomerase
  • Parotid Neoplasms / metabolism*
  • Parotid Neoplasms / mortality*
  • Parotid Neoplasms / pathology
  • Peptidylprolyl Isomerase / metabolism*
  • Retrospective Studies
  • Survival Rate
  • Young Adult
  • beta Catenin / metabolism*

Substances

  • NIMA-Interacting Peptidylprolyl Isomerase
  • beta Catenin
  • Cyclin D1
  • PIN1 protein, human
  • Peptidylprolyl Isomerase