Best Practice & Research Clinical Endocrinology & Metabolism
Volume 22, Issue 2 , Pages 223-228, April 2008

Expression of steroidogenic enzymes and sex-steroid receptors in human prostate

Oncology and Molecular Endocrinology Laboratory Research Center, Laval University Hospital Research Center (CRCHUL) and Laval University, 2705 Laurier boulevard, Quebec G1V 4G2, Canada

Identification of the cell types expressing the steroidogenic enzymes and sex steroid receptors in the human prostate has recently been performed using immunocytochemistry and in-situ hybridization. The enzymes 3β-hydroxysteroid dehydrogenase (3β-HSD), which converts dehydroepiandrosterone (DHEA) into androstenedione, and type 5 17β-HSD, which catalyzes the reduction of androstenedione to testosterone, have been localized in basal cells of alveoli as well as in stromal cells and endothelial cells of blood vessels. On the other hand, type-2 5α-reductase, which converts testosterone into the most potent androgen dihydrotestosterone (DHT), has been mostly observed in the luminal cells in alveoli. Aromatase, which converts testosterone into estradiol, has also been found to be expressed in the luminal cells of the alveoli as well as in stromal cells. Androgen receptor (AR) has been localized in luminal cell nuclei of alveoli and a large number of stromal cells, while estrogen receptor β has been detected in both basal and luminal cells in alveoli and also in stromal cells.

Key words: steroidogenic enzymes, sex steroid receptors, prostate, androgens, estrogens, immunocytochemistry, in-situ hybridization

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PII: S1521-690X(08)00032-8

doi:10.1016/j.beem.2008.02.004

Best Practice & Research Clinical Endocrinology & Metabolism
Volume 22, Issue 2 , Pages 223-228, April 2008