5α‐reductase type 3 enzyme in benign and malignant prostate
暂无分享,去创建一个
J. Mohler | M. Titus | Varun Maher | A. Godoy | O. Kozyreva | Yun Li | Gary J. Smith
[1] C. Sander,et al. Distinct patterns of dysregulated expression of enzymes involved in androgen synthesis and metabolism in metastatic prostate cancer tumors. , 2012, Cancer research.
[2] M. Dowsett,et al. Clinical and biochemical consequences of CYP17A1 inhibition with abiraterone given with and without exogenous glucocorticoids in castrate men with advanced prostate cancer. , 2012, The Journal of clinical endocrinology and metabolism.
[3] Rui Li,et al. Dihydrotestosterone synthesis bypasses testosterone to drive castration-resistant prostate cancer , 2011, Proceedings of the National Academy of Sciences.
[4] J. Mohler,et al. 5α‐reductase type 3 expression in human benign and malignant tissues: A comparative analysis during prostate cancer progression , 2011, The Prostate.
[5] J. Mohler,et al. Potential Prostate Cancer Drug Target: Bioactivation of Androstanediol by Conversion to Dihydrotestosterone , 2011, Clinical Cancer Research.
[6] H. Freeze,et al. SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder , 2010, Cell.
[7] K. Tomer,et al. Atmospheric pressure photoionization tandem mass spectrometry of androgens in prostate cancer. , 2010, Analytical chemistry.
[8] Dan S. Tawfik,et al. Enzyme promiscuity: a mechanistic and evolutionary perspective. , 2010, Annual review of biochemistry.
[9] V. Langlois,et al. Evolution of steroid-5alpha-reductases and comparison of their function with 5beta-reductase. , 2010, General and comparative endocrinology.
[10] P. Walsh,et al. Chemoprevention of prostate cancer. , 2010, The New England journal of medicine.
[11] D. Tindall,et al. Effect of dutasteride on the risk of prostate cancer. , 2010, The New England journal of medicine.
[12] Melani-Ivy Samson,et al. Sequential transformation of 4-androstenedione into dihydrotestosterone in prostate carcinoma (DU-145) cells indicates that 4-androstenedione and not testosterone is the substrate of 5α-reductase , 2010, Hormone molecular biology and clinical investigation.
[13] D. Tindall,et al. Effects of the 5 alpha‐reductase inhibitor dutasteride on gene expression in prostate cancer xenografts , 2009, The Prostate.
[14] C. Morrison,et al. Central quadrant procurement of radical prostatectomy specimens , 2009, The Prostate.
[15] G. Wilding,et al. Phase II study of Dutasteride for recurrent prostate cancer during androgen deprivation therapy. , 2009, The Journal of urology.
[16] R. Rittmaster,et al. Effect of dutasteride on intraprostatic androgen levels in men with benign prostatic hyperplasia or prostate cancer. , 2008, Urology.
[17] M. Gleave,et al. Androgen levels increase by intratumoral de novo steroidogenesis during progression of castration-resistant prostate cancer. , 2008, Cancer research.
[18] P. Nelson,et al. Maintenance of intratumoral androgens in metastatic prostate cancer: a mechanism for castration-resistant tumor growth. , 2008, Cancer research.
[19] Yusuke Nakamura,et al. Novel 5 alpha-steroid reductase (SRD5A3, type-3) is overexpressed in hormone-refractory prostate cancer. , 2008, Cancer science.
[20] Yusuke Nakamura,et al. Novel 5α‐steroid reductase (SRD5A3, type‐3) is overexpressed in hormone‐refractory prostate cancer , 2007 .
[21] R. Rittmaster,et al. The effect of dutasteride on intraprostatic dihydrotestosterone concentrations in men with benign prostatic hyperplasia , 2007, Prostate Cancer and Prostatic Diseases.
[22] J. Isaacs,et al. Pharmacologic Basis for the Enhanced Efficacy of Dutasteride against Prostatic Cancers , 2006, Clinical Cancer Research.
[23] T. Golub,et al. Increased expression of genes converting adrenal androgens to testosterone in androgen-independent prostate cancer. , 2006, Cancer research.
[24] S. Frye. Discovery and clinical development of dutasteride, a potent dual 5alpha-reductase inhibitor. , 2006, Current topics in medicinal chemistry.
[25] D. Peehl,et al. Identification of the Major Oxidative 3α-Hydroxysteroid Dehydrogenase in Human Prostate That Converts 5α-Androstane-3α,17β-diol to 5α-Dihydrotestosterone: A Potential Therapeutic Target for Androgen-Dependent Disease , 2006 .
[26] D. Peehl,et al. Identification of the major oxidative 3alpha-hydroxysteroid dehydrogenase in human prostate that converts 5alpha-androstane-3alpha,17beta-diol to 5alpha-dihydrotestosterone: a potential therapeutic target for androgen-dependent disease. , 2006, Molecular endocrinology.
[27] K. Tomer,et al. Testosterone and Dihydrotestosterone Tissue Levels in Recurrent Prostate Cancer , 2005, Clinical Cancer Research.
[28] M. Schell,et al. Steroid 5α-Reductase Isozymes I and II in Recurrent Prostate Cancer , 2005, Clinical Cancer Research.
[29] D. Troyer,et al. Differential alterations in 5α‐reductase type 1 and type 2 levels during development and progression of prostate cancer , 2005 .
[30] M. Schell,et al. Steroid 5alpha-reductase isozymes I and II in recurrent prostate cancer. , 2005, Clinical cancer research : an official journal of the American Association for Cancer Research.
[31] D. Troyer,et al. Differential alterations in 5alpha-reductase type 1 and type 2 levels during development and progression of prostate cancer. , 2005, The Prostate.
[32] R. Auchus. The backdoor pathway to dihydrotestosterone , 2004, Trends in Endocrinology & Metabolism.
[33] D. Tindall,et al. Chemoprevention of prostate cancer in men at high risk: rationale and design of the reduction by dutasteride of prostate cancer events (REDUCE) trial. , 2004, The Journal of urology.
[34] M. Gleave,et al. Effect of the dual 5α-reductase inhibitor dutasteride on markers of tumor regression in prostate cancer , 2004 .
[35] G. Cunningham,et al. Marked suppression of dihydrotestosterone in men with benign prostatic hyperplasia by dutasteride, a dual 5alpha-reductase inhibitor. , 2004, The Journal of clinical endocrinology and metabolism.
[36] Desok Kim,et al. The Androgen Axis in Recurrent Prostate Cancer , 2004, Clinical Cancer Research.
[37] M. Carducci,et al. Phase I and clinical pharmacology of a type I and II, 5-alpha-reductase inhibitor (LY320236) in prostate cancer: elevation of estradiol as possible mechanism of action. , 2004, Urology.
[38] R. Auchus,et al. 5α-reduced C21 steroids are substrates for human cytochrome P450c17 , 2003 .
[39] Jun Luo,et al. Decreased gene expression of steroid 5 alpha‐reductase 2 in human prostate cancer: Implications for finasteride therapy of prostate carcinoma , 2003, The Prostate.
[40] Michael M Lieber,et al. The influence of finasteride on the development of prostate cancer. , 2003, The New England journal of medicine.
[41] R. Auchus,et al. 5alpha-reduced C21 steroids are substrates for human cytochrome P450c17. , 2003, Archives of biochemistry and biophysics.
[42] Jean D. Wilson. The role of 5a-reduction in steroid hormone physiology , 2001 .
[43] D. Russell,et al. Unexpected Virilization in Male Mice Lacking Steroid 5α-Reductase Enzymes. , 2001, Endocrinology.
[44] D. Russell,et al. Unexpected virilization in male mice lacking steroid 5 alpha-reductase enzymes. , 2001, Endocrinology.
[45] J. Wilson. The role of 5alpha-reduction in steroid hormone physiology. , 2001, Reproduction, fertility, and development.
[46] Michael E. Burczynski,et al. Human 3α-hydroxysteroid dehydrogenase isoforms (AKR1C1–AKR1C4) of the aldo-keto reductase superfamily: functional plasticity and tissue distribution reveals roles in the inactivation and formation of male and female sex hormones , 2000 .
[47] N. Palackal,et al. Human 3alpha-hydroxysteroid dehydrogenase isoforms (AKR1C1-AKR1C4) of the aldo-keto reductase superfamily: functional plasticity and tissue distribution reveals roles in the inactivation and formation of male and female sex hormones. , 2000, The Biochemical journal.
[48] E. Fearon,et al. Cancer progression , 1999, Current Biology.
[49] D. Poirier,et al. Separation by thin-layer chromatography of the most common androgen-derived C19 steroids formed by mammalian cells☆ , 1999, Steroids.
[50] P. Span,et al. Selectivity of finasteride as an in vivo inhibitor of 5alpha-reductase isozyme enzymatic activity in the human prostate. , 1999, The Journal of urology.
[51] M. Poutanen,et al. Characterization of 17B‐hydroxysteroid dehydrogenase isoenzyme expression in benign and malignant human prostate , 1996 .
[52] M. Poutanen,et al. Characterization of 17beta-hydroxysteroid dehydrogenase isoenzyme expression in benign and malignant human prostate. , 1996, International journal of cancer.
[53] S. Frye,et al. Mechanism of time-dependent inhibition of 5 alpha-reductases by delta 1-4-azasteroids: toward perfection of rates of time-dependent inhibition by using ligand-binding energies. , 1995, Biochemistry.
[54] G. Andriole,et al. Treatment with finasteride following radical prostatectomy for prostate cancer. , 1995, Urology.
[55] J. D. Stuart,et al. 17 beta-(N-tert-butylcarbamoyl)-4-aza-5 alpha-androstan-1-en-3-one is an active site-directed slow time-dependent inhibitor of human steroid 5 alpha-reductase 1. , 1994, Biochemistry.
[56] D. Russell,et al. Characterization of Chinese hamster ovary cell lines expressing human steroid 5 alpha-reductase isozymes. , 1993, The Journal of biological chemistry.
[57] J. Isaacs,et al. Response of rat and human prostatic cancers to the novel 5α‐reductase inhibitor, SK&F 105657 , 1992 .
[58] J. Isaacs,et al. Response of rat and human prostatic cancers to the novel 5 alpha-reductase inhibitor, SK&F 105657. , 1992, The Prostate.
[59] J. Epstein. Evaluation of Radical Prostatectomy Capsular Margins of Resection: The Significance of Margins Designated as Negative, Closely Approaching, and Positive , 1990, The American journal of surgical pathology.
[60] D. Thompson,et al. Effects of finasteride (MK-906), a 5 alpha-reductase inhibitor, on circulating androgens in male volunteers. , 1990, The Journal of clinical endocrinology and metabolism.
[61] M. Brandt,et al. Mechanistic studies with solubilized rat liver steroid 5 alpha-reductase: elucidation of the kinetic mechanism. , 1990, Biochemistry.
[62] K. Roberts,et al. Steroidal inhibitors of prostatic 5α-reductase: Structure-activity relationships , 1978 .