Increased transglutaminase 2 and GLUT-1 expression in breast tumors not susceptible to chemoprevention with antioxidants

Tumori. 2009 Mar-Apr;95(2):227-32. doi: 10.1177/030089160909500215.

Abstract

Goals: Expression of GLUT-1 and transglutaminase 2 is increased in aggressive breast cancer, whereas claudin-1, which is expressed in normal tissues, is absent in such tumors. This experimental study was undertaken to establish the aggressiveness and prognosis of DMBA-induced mammary tumors in female Wistar rats based on the assessment of these markers.

Materials and methods: The rats were divided into two groups, a control group (n = 70) and a chemoprevention group (n = 70). Breast tumors were induced in both groups by administration of 7,12-dimethylbenz[a] anthracene (DMBA). The chemoprevention group also received alpha-tocopherol and a solution of micronutrients containing ascorbic acid and selenium. Neoplastic lesions of both groups were randomly selected for immunohistochemical assessment of the expression of GLUT-1, transglutaminase 2 and claudin-1.

Results: A higher proportion of mammary tumors expressed GLUT-1 and transglutaminase 2 in the chemoprevention group. Claudin-1 expression was absent in all tumors of both groups.

Conclusions: These results are suggestive of increased aggressiveness of tumors not susceptible to chemoprevention by the agents used in this study.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 9,10-Dimethyl-1,2-benzanthracene
  • Animals
  • Anticarcinogenic Agents / administration & dosage
  • Anticarcinogenic Agents / pharmacology*
  • Antioxidants / administration & dosage
  • Antioxidants / pharmacology*
  • Ascorbic Acid / pharmacology
  • Biomarkers, Tumor / metabolism*
  • Breast Neoplasms / chemically induced
  • Breast Neoplasms / enzymology*
  • Breast Neoplasms / prevention & control*
  • Carcinogens
  • Female
  • GTP-Binding Proteins / drug effects*
  • Gene Expression Regulation, Enzymologic / drug effects
  • Gene Expression Regulation, Neoplastic / drug effects
  • Glucose Transporter Type 1 / drug effects*
  • Immunohistochemistry
  • Protein Glutamine gamma Glutamyltransferase 2
  • Random Allocation
  • Rats
  • Rats, Wistar
  • Selenium Compounds / pharmacology
  • Transglutaminases / drug effects*
  • Treatment Failure
  • alpha-Tocopherol / pharmacology

Substances

  • Anticarcinogenic Agents
  • Antioxidants
  • Biomarkers, Tumor
  • Carcinogens
  • Glucose Transporter Type 1
  • Selenium Compounds
  • Tgm2 protein, rat
  • 9,10-Dimethyl-1,2-benzanthracene
  • Protein Glutamine gamma Glutamyltransferase 2
  • Transglutaminases
  • GTP-Binding Proteins
  • alpha-Tocopherol
  • Ascorbic Acid