Immunohistochemical characterization of N-methyl-N-nitrosourea-induced mammary tumours of Sprague-Dawley rats

In Vivo. 2013 Nov-Dec;27(6):793-801.

Abstract

Background: Single dose of N-methyl-N-nitrosourea (MNU) was shown to induce malignant tumours in susceptible rat strains. However, such tumours are not well-characterized.

Material and methods: We characterized MNU-induced tumours in Sprague-Dawley rats using ultrasonographic, radiographic and immunohistochemical (IHC) methods.

Results: In 27 rats, 41 tumours developed, appearing ultrasonographically as hypodense, non-homogenic areas with signal enhancement at their periphery. Out of these, 39 were of malignant epithelial origin, with an IHC phenotype closely-resembling that of human invasive ductal breast carcinoma. One case was diagnosed as carcinosarcoma. IHC analysis revealed that Ki-67 antigen expression correlated positively with tumour volume (r=0.40, p=0.0079). Moreover, tumours with α-smooth muscle actin in the tumour stroma were characterized by a higher proliferative rate as compared to those without its expression (p<0.05).

Conclusion: This rat model of chemical carcinogenesis may be suitable for examining breast cancer development and progression.

Keywords: Breast cancer; MNU; immunohistochemistry; rat carcinoma; rodent models.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carcinoma, Ductal, Breast / chemically induced
  • Carcinoma, Ductal, Breast / metabolism*
  • Carcinoma, Ductal, Breast / pathology
  • Carcinosarcoma / chemically induced
  • Carcinosarcoma / metabolism*
  • Carcinosarcoma / pathology
  • Cdh1 Proteins / metabolism
  • Female
  • Humans
  • Immunohistochemistry
  • Keratins / metabolism
  • Mammary Neoplasms, Experimental / chemically induced
  • Mammary Neoplasms, Experimental / metabolism*
  • Mammary Neoplasms, Experimental / pathology
  • Methylnitrosourea
  • Paraffin Embedding
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Progesterone / metabolism
  • Tumor Burden

Substances

  • Cdh1 Proteins
  • Receptors, Progesterone
  • Keratins
  • Methylnitrosourea