Expression of the GLUT1 glucose transporter and p53 in carcinomas of the pancreatobiliary tract

Pathol Res Pract. 2010 Jan 15;206(1):24-9. doi: 10.1016/j.prp.2009.07.018. Epub 2009 Oct 12.

Abstract

Only few studies have evaluated the usefulness of the GLUT1 and p53 status of pancreatobiliary tract carcinomas in revealing tumorigenesis. We studied GLUT1 and p53 immunoexpression in a total of 355 cases of the pancreatobiliary carcinoma to determine the biological significance of GLUT1 and p53 expression. Positive expression of GLUT1 was identified in 38 out of 67 (57.7%) ampulla of Vater (AV) carcinomas, in 27 out of 52 (51.8%) pancreatic (PA) carcinomas, in 38 out of 121 (31.4%) extrahepatic bile duct (EBD) carcinomas, and in 53 out of 115 (46.5%) gallbladder (GB) carcinomas. GLUT1 expression in pancreatobiliary carcinomas showed some positive correlation with histological grade, T stage, N stage, TNM stage, and lymphatic invasion. However, p53 expression showed no correlation with any prognostic factors. In the Kaplan-Meier test, positive GLUT1 expression was a poor prognostic factor in the pancreatobiliary tract cancers; however, only GB cancers were statistically significant (P=0.002). Our results suggest that GLUT1 expression in the AV, EBD, and GB carcinomas is associated with some prognostic factors, and GLUT1 expression is associated with a worse prognosis in the patients with GB carcinomas.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Ampulla of Vater / metabolism*
  • Ampulla of Vater / pathology
  • Bile Duct Neoplasms / metabolism*
  • Bile Duct Neoplasms / mortality
  • Bile Duct Neoplasms / pathology
  • Bile Ducts, Extrahepatic / metabolism*
  • Bile Ducts, Extrahepatic / pathology
  • Carcinoma / metabolism*
  • Carcinoma / pathology
  • Female
  • Gallbladder Neoplasms / metabolism*
  • Gallbladder Neoplasms / mortality
  • Gallbladder Neoplasms / pathology
  • Glucose Transporter Type 1 / metabolism*
  • Humans
  • Immunohistochemistry
  • Kaplan-Meier Estimate
  • Male
  • Middle Aged
  • Neoplasm Staging
  • Pancreatic Neoplasms / metabolism*
  • Pancreatic Neoplasms / mortality
  • Pancreatic Neoplasms / pathology
  • Prognosis
  • Proportional Hazards Models
  • Tumor Suppressor Protein p53 / metabolism*

Substances

  • Glucose Transporter Type 1
  • SLC2A1 protein, human
  • Tumor Suppressor Protein p53