A Small Composite Probasin Promoter Confers High Levels of Prostate-Specific Gene Expression through Regulation by Androgens and Glucocorticoids in Vitro and in Vivo**This work was supported by R01-DK-55748 from the NIH and the Frances Williams Preston Laboratories of the T. J. Martell Foundation. Transgenic mice were bred by the Transgenic Core/ES Cell Shared Resource of the Vanderbilt-Ingram Cancer Center (NCI Grant 2P30-CA-68485–05).

Author:

Zhang JianFeng123,Thomas Tania Z.13,Kasper Susan123,Matusik Robert J.12345

Affiliation:

1. Departments of Urologic Surgery (J.Z., T.Z.T., S.K., R.J.M.) Nashville, Tennessee 37232

2. Cell Biology (J.Z., S.K., R.J.M.), Nashville, Tennessee 37232

3. The Vanderbilt Prostate Cancer Center (J.Z., T.Z.T., S.K., R.J.M.), Nashville, Tennessee 37232

4. Center for Reproductive Biology Research (R.J.M.), Nashville, Tennessee 37232

5. The Vanderbilt-Ingram Cancer Center (R.J.M.), Nashville, Tennessee 37232

Publisher

The Endocrine Society

Subject

Endocrinology

Reference42 articles.

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2. Increased androgen receptor activity and altered c-myc expression in prostate cancer cells after long-term androgen deprivation.;Kokontis;Cancer Res,1994

3. A DNA sequence of 15 base pairs is sufficient to mediate both glucocorticoid and progesterone induction of gene expression.;Shrahle;Proc Natl Acad Sci USA,1987

4. Characterization of response elements for androgens, glucocorticoids and progestins in mouse mammary tumour virus.;Ham;Nucleic Acids Res,1988

5. Characterization and cloning of rat dorsal prostate mRNAs. Androgen regulation of two closely related abundant mRNAs.;Dodd;J Biol Chem,1983

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