A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Constant expression of cyclooxygenase-2 gene in prostate and the lower urinary tract of estrogen-treated male rats
Tekijät: Luo C, Strauss L, Ristimaki A, Streng T, Santti R
Kustantaja: VERLAG Z NATURFORSCH
Julkaisuvuosi: 2001
Lehti:: Zeitschrift fur naturforschung section c: a journal of biosciences
Tietokannassa oleva lehden nimi: ZEITSCHRIFT FUR NATURFORSCHUNG C-A JOURNAL OF BIOSCIENCES
Lehden akronyymi: Z NATURFORSCH C
Vuosikerta: 56
Numero: 5-6
Aloitussivu: 455
Lopetussivu: 463
Sivujen määrä: 9
ISSN: 0939-5075
Tiivistelmä
Expression of cyclooxygenase-2 (E. C. 1.14.99.1) in prostate and the lower urinary tract (LUT) of the neonatally estrogenized male rat has been studied by using a COX-2's PCR fragment of 724 nt spanning 3 introns and a 478nt internal standard for quantitative RT-PCR. The same fragment of 724 nt was used for RNA probe in Northern hybridization. Neonatal estrogenization (10 mug/day of diethylstilbestrol on days 1-5) had no effect on COX-2 expression in prostatic urethra, prostatic lobes. or bladder. Acute estrogen treatment of castrated animals did not induce COX-2 expression. either. In addition the differential expression of basal level of COX-2 in the different lobes of prostate in normal rat was demonstrated. Our results suggest a constant expression of COX-2 gene in prostate and the lower urinary tract of the neonatally estrogenized (neoDES) rats. The present study indicates that the increased expression of COX-2 is probably not essential for the estrogen-driven development of stromal inflammation or hyperplastic and dysplastic alterations in the prostate of neoDES rats.
Expression of cyclooxygenase-2 (E. C. 1.14.99.1) in prostate and the lower urinary tract (LUT) of the neonatally estrogenized male rat has been studied by using a COX-2's PCR fragment of 724 nt spanning 3 introns and a 478nt internal standard for quantitative RT-PCR. The same fragment of 724 nt was used for RNA probe in Northern hybridization. Neonatal estrogenization (10 mug/day of diethylstilbestrol on days 1-5) had no effect on COX-2 expression in prostatic urethra, prostatic lobes. or bladder. Acute estrogen treatment of castrated animals did not induce COX-2 expression. either. In addition the differential expression of basal level of COX-2 in the different lobes of prostate in normal rat was demonstrated. Our results suggest a constant expression of COX-2 gene in prostate and the lower urinary tract of the neonatally estrogenized (neoDES) rats. The present study indicates that the increased expression of COX-2 is probably not essential for the estrogen-driven development of stromal inflammation or hyperplastic and dysplastic alterations in the prostate of neoDES rats.
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