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|Title:||Receptor Isoforms That Mediate Estrogen and Progestagen Action in the Female Lower Urinary Tract|
|Authors:||Tincello, Douglas G.|
Taylor, Anthony H.
Spurling, Susan M.
Bell, Stephen C.
|Citation:||Journal of Urology, 2009, 181 (3), pp. 1474-1482.|
|Abstract:||Purpose : Bladder symptoms can be ameliorated by sex steroids but to our knowledge the mechanism of action is unknown. Previous studies of steroid receptor expression in the bladder did not indicate receptor subtype expression. We report the distribution of estrogen and progesterone receptor isoforms in the female lower urinary tract. Materials and Methods : Prospectively recruited women undergoing routine urogynecological or gynecological surgery provided cold cup biopsy samples from the bladder dome, trigone, and proximal and distal urethra. The samples were immediately frozen or fixed in formalin. After RNA extraction transcripts for estrogen receptor α and β, and progesterone receptor A and B were noted on reverse transcriptase-polymerase chain reaction using isoform specific primers. The precise cellular localization of receptor proteins and their relative levels were assessed by immunochemistry in formalin fixed tissue sections with isoform specific antibodies. Results : Nine premenopausal and 10 postmenopausal women were recruited into the study. Two postmenopausal women on hormone replacement therapy. Estrogen receptor α and β, and progesterone receptor A and B transcripts were detected in whole bladder extracts. Nuclear estrogen receptor α immunoreactivity was present in squamous epithelium but absent from transitional epithelium. Estrogen receptor β immunoreactivity was expressed in squamous and transitional cell epithelium. Nuclear progesterone receptor expression was present in urethral squamous epithelium only. Progesterone receptor expression was greater in premenopausal women and in postmenopausal women on estrogen. Conclusions : Estrogen receptor α and β genes are transcribed in bladder tissue but only estrogen receptor β is translated into protein, suggesting that the urothelium responds to endogenous estrogen via estrogen receptor β. Progesterone receptor expression is confined to urethral squamous epithelium and the major isoform is progesterone receptor A.|
|Description:||This is the author's final draft of the paper published as Journal of Urology, 2009, 181 (3), pp. 1474-1482. The final version is available from http://www.jurology.com/home. Doi: 10.1016/j.juro.2008.10.104|
|Appears in Collections:||Published Articles, Dept. of Cancer Studies and Molecular Medicine|
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