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Inhibition of prolactin-induced mammary cancer in C3Hf (XVII) mice with the trans isomer of bromotriphenylethylene

Cancer Res. 1980 May;40(5):1674-9.

Abstract

C3Hf (XVII) mice never develop spontaneous mammary tumors. However, the transplantation of an isologous pituitary gland under their kidney capsule is followed by a 10-fold increase in serum and pituitary prolactin content (180 ng/ml and 20 micrograms/mg of tissue, respectively), concomitant with an increase of prolactin receptors in mammary glands. Under these conditions, mammary tumors appear in 90% of the mice. If a racemic brominated triphenylethylene, i.e., broparestrol, is administered, serum and pituitary prolactin decrease rapidly (10 ng/ml and 4 micrograms/mg of tissue, respectively), and prolactin receptors in the mammary gland are markedly reduced. This compound also inhibits the development of normal mammary glands, prevents mammary carcinogenesis, and unexpectedly causes a significant atrophy of the ovaries. Our study confirms that prolactin is a key hormone involved in murine mammary carcinogenesis and that it can act directly on the mammary gland by stimulaing the level of its own receptor.

MeSH terms

  • Animals
  • Female
  • Mammary Neoplasms, Experimental / chemically induced*
  • Mice
  • Mice, Inbred C3H
  • Pituitary Gland / transplantation
  • Prolactin* / antagonists & inhibitors
  • Prolactin* / blood
  • Receptors, Cell Surface / metabolism
  • Stereoisomerism
  • Stilbenes / pharmacology*

Substances

  • Receptors, Cell Surface
  • Stilbenes
  • broparoestrol
  • Prolactin