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

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.

• Authors: M Drosdowsky, M Edery, M Guggiari, A Montes-Rendon, G Rudali, C Vives
• Journal: Cancer research (Cancer Res) Vol. 40 Issue 5 Pg. 1674-9 (May 1980) ISSN: 0008-5472 [Print] United States
• PMID: 6245799 (Publication Type: Journal Article)

Chemical References

• Receptors, Cell Surface
• Stilbenes
• broparoestrol
• Prolactin

Topics

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