Yeungnam Univ J Med.  2006 Jun;23(1):62-70.

Effect of Progesterone on COX-2 Expression and Proliferation of Prostate Stromal Cell

Affiliations
  • 1Senior grade, College of Medicine, Yeungnam University, Daegu, Korea.
  • 2Department of Pharmacology, College of Medicine, Yeungnam University, Daegu, Korea. hcchoi@med.yu.ac.kr

Abstract

BACKGROUND: Benign prostatic hyperplasia (BPH) is the most common benign tumor in older men; the etiology of this disease remains poorly understood. Testosterone and dihydrotestosterone (DHT) both act as androgen via a single androgen receptor. Testosterone is converted to DHT by 5alpha-reductase in prostatic stromal cells. Progesterone has been reported to inhibit DHT conversion; howevwe, its effect on prostatic stromal cells remains to be elucidated. MATERILAS AND METHODS: In this experiment, we investigated the effect of progesterone on androgen receptor expression induced by DHT. We also tested the effect of progesterone on cyclooxygenase-2 (COX-2) expression, as well as prostate stromal cell proliferation using the cell count kit-8.
RESULTS
Progesterone did not cause an increase of prostate stromal cell proliferation. The mRNA expression of the androgen receptor and COX-2 were not changed by progesterone; the expressions of androgen receptor and COX-2 proteins were decreased by progesterone in prostate stromal cells.
CONCLUSION
These results suggest that in prostate stromal cells, progesterone decreases androgen receptor protein expression, which results in decrement of COX-2 protein expression. This effect might be mediated by post-transcriptional regulation.

Keyword

Prostate stromal cell; Progesterone; Cyclooxygenase-2

MeSH Terms

Cell Count
Cyclooxygenase 2
Dihydrotestosterone
Humans
Male
Progesterone*
Prostate*
Prostatic Hyperplasia
Receptors, Androgen
RNA, Messenger
Stromal Cells*
Testosterone
Cyclooxygenase 2
Dihydrotestosterone
Progesterone
RNA, Messenger
Receptors, Androgen
Testosterone
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