MNU-induced rat mammary carcinomas: immunohistology and estrogen receptor expression

J Environ Pathol Toxicol Oncol. 2013;32(2):157-63. doi: 10.1615/jenvironpatholtoxicoloncol.2013007541.

Abstract

Environmental exposure to nitrosamines is associated with the development of cancer in a variety of target organs. One such carcinogen, N-methyl-N-nitrosurea (MNU), has long been used to induce mammary tumors in rats, which provide a useful model to study mammary carcinogenesis. However, some poorly clarified issues remain, such as the lack of a clear description of morphological patterns of tumors and the distribution and role of estrogen receptors (ERs) during tumor progression, as tumors overexpressing ERs show a paradoxical tendency to recur after ovariectomy. Mammary carcinomas were induced in Sprague-Dawley rats using MNU. The tumors were studied histologically and distribution of smooth muscle actin and ERs was studied immunohistochemically. All tumors presented both an epithelial and a myoepithelial component, demonstrated by immunohistochemical detection of smooth muscle actin. Tumors showed distinct histological patterns: well-differentiated papillary and adenoid areas and poorly differentiated solid and spindle-cell foci. Overexpression of ERs (>75% of labelled cells vs. 0-75% in control tissue) occurred in papillary and adenoid areas but not in solid and spindle-cell foci. Poorly differentiated tumor foci are likely to represent a more advanced, estrogen-independent phase in cancer progression and constitute the basis for tumor recurrence after ovariectomy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Adenocarcinoma / chemically induced
  • Adenocarcinoma / metabolism*
  • Adenocarcinoma / pathology*
  • Animals
  • Carcinogens / toxicity
  • Cell Differentiation
  • Female
  • Mammary Neoplasms, Experimental / chemically induced
  • Mammary Neoplasms, Experimental / metabolism*
  • Mammary Neoplasms, Experimental / pathology*
  • Methylnitrosourea / toxicity*
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Estrogen / metabolism*

Substances

  • Actins
  • Carcinogens
  • Receptors, Estrogen
  • smooth muscle actin, rat
  • Methylnitrosourea