Expression of enzymes involved in synthesis and metabolism of estradiol in human breast as studied by immunocytochemistry and in situ hybridization

Zhuo Li, Van Luu-The, David Poisson-Paré, Johanne Ouellet, Songyun Li, Fernand Labrie and Georges Pelletier

Oncology and Molecular Endocrinology Research Center, Laval University Hospital Research Centre (CRCHUL) and Laval University, Quebec City, Quebec, Canada.

Offprint requests to: Dr. Georges Pelletier, Oncology and Molecular Endocrinology Research Center, Laval University Hospital Research Centre (CRCHUL) and Laval University, Quebec City, Qubec, Canada, G1V 4G2. e-mail: georges.pelletier@crchul.ulaval.ca


Summary. It is well documented that human breast is actively involved in the local formation of estrogens. To determine the site(s) of action of enzymes involved in synthesis and metabolism of the most potent estrogen estradiol (E₂), we have studied the expression of the following enzymes: 3ß-hydroxysteroid dehydrogenase (3-HSD), 17ß-HSD types 1, 2, 5, 7 and 12, aromatase, steroid sulfatase (STS) and estrogen sulfotransferase (EST) 1E1 at the cellular level in breast. Both in situ hybridization and immunocytochemistry were used for enzyme localization in normal breast tissues. For immunocytochemistry, we used rabbit antibodies, while in situ hybridization studies were performed using (³⁵S)-labeled cRNA probes. Similar results were obtained with both approaches. All the enzymes (3ß-HSD; 17ß-HSD types 1, 5, 7 and 12; aromatase) involved in the conversion of circulating dehydroepiandrosterone (DHEA) to E2 as well as STS which converts estradiol sulfate (E₂-S) to E₂ have been found to be expressed in epithelial cells of acini and/or ducts as well as the stromal cells. Moreover, 17ß-HSD type 2 and EST1E1, two enzymes which inactivate E₂, have been also localized in the same cell types. The present results indicate the enzymes which play a role in the synthesis and metabolism of E₂ are expressed in both epithelial and stromal cells in human breast. Histol Histopathol 24, 273-282 (2009)

Key words: Estrogen, Human breast, Steroidogenic enzymes

DOI: 10.14670/HH-24.273