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. 1975 Aug;32(2):168-78.
doi: 10.1038/bjc.1975.146.

The effect of steroid hormones on the growth pattern and RNA synthesis in human benign prostatic hyperplasia in organ culture

Free PMC article

The effect of steroid hormones on the growth pattern and RNA synthesis in human benign prostatic hyperplasia in organ culture

I Lasnitzki et al. Br J Cancer. 1975 Aug.
Free PMC article

Abstract

The effect of testosterone, dihydrotestosterone, 3 beta-androstanediol and oestradiol-17 beta on the morphology and RNA synthesis in human benign prostatic hyperplasia (BPH) in organ culture has been investigated. In hormone treated and untreated explants alike, the epithelium multiplied to form several layers. This effect was most marked after exposure to dihydrotestosterone. In explants grown in non-supplemented medium the epithelium showed some squamous changes; testosterone or dihydrotestosterone preserved the secretory character of the epithelium while oestradiol-17 beta caused cellular degeneration. The incorporation of 3H-uridine into RNA was studied by autoradiography. In the epithelium, testosterone or dihydrotestosterone raised the uptake significantly over that measured in the control explants, oestradiol-17 beta reduced it while 3 beta-androstanediol produced similar values to those found in the control explants. The incorporation of 3H-uridine in the smooth muscle cells was increased by testosterone and decreased by oestradiol-17 beta. A comparison with normal rat prostatic epithelium in organ culture showed that in the absence of androgens the incorporation of 3H-uridine was lower than in BPH and the effect of testosterone correspondingly greater. The results suggest that although the growth of human BPH in organ culture appears to be androgen dependent, it still remains hormone sensitive and can be influenced by steroid hormones in a similar manner to that in rat prostatic gland. They further show that the smooth muscle of the stroma is also hormone sensitive, a point which should be considered in the hormonal management of benign prostatic hyperplasia.

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