Literature DB >> 9834458

Identification of genes expressed in the rat prostate that are modulated differently by castration and Finasteride treatment.

D M Avila1, S A Fuqua, F W George, M J McPhaul.   

Abstract

In mammals, testosterone and 5alpha-dihydrotestosterone (DHT) are the principal male hormones (androgens). Testosterone is the most abundant circulating androgen, and is converted in specific tissues to DHT by the 5alpha-reductase enzymes. Although each of these androgens binds to the same receptor protein (androgen receptor, AR), each exerts biologically distinct effects. Theories to explain the specific effects of testosterone and DHT have centered on kinetic differences of binding of androgens to the receptor or differences in the metabolic fates of the two hormones. In the current experiments, differential display PCR (ddPCR) was used to identify genes regulated differently by testosterone and DHT. Adult male rats were treated as follows: castrated, treated with Finasteride (an inhibitor of 5alpha-reductase) or left intact for ten days. RNA was prepared from the dissected prostates of these animals and used for ddPCR. Genes exhibiting four distinct patterns of regulation were observed among the mRNAs. Class 1 genes showed equivalent expression in intact and Finasteride-treated animals, but were absent in castrated animals (mRNAs D1, D2, D6, D10). Class 2 genes showed higher expression in intact animals, intermediate levels following Finasteride treatment, but were absent in castrated animals (mRNA D8). Two classes of gene were particularly intriguing: class 3 showed gene expression only in the intact animal (mRNA D7, D9) and class 4 showed increased gene expression following Finasteride treatment (mRNA D3). While the patterns observed for some of these genes (e.g. D8) suggest that the different biological effects of testosterone and DHT may be due to the lower affinity of the AR for testosterone and limiting tissue concentrations of androgen, our results also suggest that some genes expressed in the rat prostate may be regulated in fundamentally different ways in response to testosterone and DHT.

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Year:  1998        PMID: 9834458     DOI: 10.1677/joe.0.1590403

Source DB:  PubMed          Journal:  J Endocrinol        ISSN: 0022-0795            Impact factor:   4.286


  5 in total

1.  Testosterone, not 5α-dihydrotestosterone, stimulates LRH-1 leading to FSH-independent expression of Cyp19 and P450scc in granulosa cells.

Authors:  Yan-Guang Wu; Jill Bennett; Deepika Talla; Carlos Stocco
Journal:  Mol Endocrinol       Date:  2011-01-27

2.  Inhibition of 5alpha-reductase in rat prostate reveals differential regulation of androgen-response gene expression by testosterone and dihydrotestosterone.

Authors:  S S Dadras; X Cai; I Abasolo; Z Wang
Journal:  Gene Expr       Date:  2001

3.  Testosterone-dependent interaction between androgen receptor and aryl hydrocarbon receptor induces liver receptor homolog 1 expression in rat granulosa cells.

Authors:  Yanguang Wu; Sarah C Baumgarten; Ping Zhou; Carlos Stocco
Journal:  Mol Cell Biol       Date:  2013-05-20       Impact factor: 4.272

4.  Impact of the Processes of Total Testicular Regression and Recrudescence on the Epididymal Physiology of the Bat Myotis nigricans (Chiroptera: Vespertilionidae).

Authors:  Mateus R Beguelini; Rejane M Góes; Paula Rahal; Eliana Morielle-Versute; Sebastião R Taboga
Journal:  PLoS One       Date:  2015-06-09       Impact factor: 3.240

Review 5.  Improving intermittent androgen deprivation therapy: lessons learned from basic and translational research.

Authors:  Rahul A Parikh; Laura E Pascal; Benjamin J Davies; Zhou Wang
Journal:  Asian J Androl       Date:  2014 Jul-Aug       Impact factor: 3.285

  5 in total

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