Literature DB >> 27519632

A new dawn for androgens: Novel lessons from 11-oxygenated C19 steroids.

Elzette Pretorius1, Wiebke Arlt2, Karl-Heinz Storbeck3.   

Abstract

The abundant adrenal C19 steroid 11β-hydroxyandrostenedione (11OHA4) has been written off as a dead-end product of adrenal steroidogenesis. However, recent evidence has demonstrated that 11OHA4 is the precursor to the potent androgenic 11-oxygenated steroids, 11-ketotestosterone and 11-ketodihydrotestosterone, that bind and activate the human androgen receptor similarly to testosterone and DHT. The significance of this discovery becomes apparent when considering androgen dependent diseases such as castration resistant prostate cancer and diseases associated with androgen excess, e.g. congenital adrenal hyperplasia and polycystic ovary syndrome. In this review we describe the production and metabolism of 11-oxygenated steroids. We subsequently discuss their androgenic activity and highlight the putative role of these androgens in disease states.
Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  11-Ketodihydrotestosterone (11KDHT); 11-Ketotestosterone (11KT); Adrenal androgens; Castration resistant prostate cancer (CRPC); Congenital adrenal hyperplasia (CAH); Polycystic ovary syndrome (PCOS)

Mesh:

Substances:

Year:  2016        PMID: 27519632     DOI: 10.1016/j.mce.2016.08.014

Source DB:  PubMed          Journal:  Mol Cell Endocrinol        ISSN: 0303-7207            Impact factor:   4.102


  40 in total

1.  Adrenal androgens rescue prostatic dihydrotestosterone production and growth of prostate cancer cells after castration.

Authors:  Yue Wu; Li Tang; Gissou Azabdaftari; Elena Pop; Gary J Smith
Journal:  Mol Cell Endocrinol       Date:  2019-02-23       Impact factor: 4.102

Review 2.  Human steroid biosynthesis, metabolism and excretion are differentially reflected by serum and urine steroid metabolomes: A comprehensive review.

Authors:  Lina Schiffer; Lise Barnard; Elizabeth S Baranowski; Lorna C Gilligan; Angela E Taylor; Wiebke Arlt; Cedric H L Shackleton; Karl-Heinz Storbeck
Journal:  J Steroid Biochem Mol Biol       Date:  2019-07-27       Impact factor: 4.292

3.  Bacterial steroid-17,20-desmolase is a taxonomically rare enzymatic pathway that converts prednisone to 1,4-androstanediene-3,11,17-trione, a metabolite that causes proliferation of prostate cancer cells.

Authors:  Lindsey K Ly; Joe L Rowles; Hans Müller Paul; João M P Alves; Camdon Yemm; Patricia M Wolf; Saravanan Devendran; Matthew E Hudson; David J Morris; John W Erdman; Jason M Ridlon
Journal:  J Steroid Biochem Mol Biol       Date:  2019-12-20       Impact factor: 4.292

Review 4.  The way toward adulthood for females with nonclassic congenital adrenal hyperplasia.

Authors:  Georgia Ntali; Sokratis Charisis; Christo F Kylafi; Evangelia Vogiatzi; Lina Michala
Journal:  Endocrine       Date:  2021-04-14       Impact factor: 3.633

Review 5.  Monogenic Disorders of Adrenal Steroidogenesis.

Authors:  Elizabeth S Baranowski; Wiebke Arlt; Jan Idkowiak
Journal:  Horm Res Paediatr       Date:  2018-06-06       Impact factor: 2.852

Review 6.  Structural and Functional Biology of Aldo-Keto Reductase Steroid-Transforming Enzymes.

Authors:  Trevor M Penning; Phumvadee Wangtrakuldee; Richard J Auchus
Journal:  Endocr Rev       Date:  2019-04-01       Impact factor: 19.871

Review 7.  New perspectives on the definition and management of polycystic ovary syndrome.

Authors:  R Pasquali; A Gambineri
Journal:  J Endocrinol Invest       Date:  2018-01-23       Impact factor: 4.256

8.  Structural and biochemical characterization of 20β-hydroxysteroid dehydrogenase from Bifidobacterium adolescentis strain L2-32.

Authors:  Heidi L Doden; Rebecca M Pollet; Sean M Mythen; Zdzislaw Wawrzak; Saravanan Devendran; Isaac Cann; Nicole M Koropatkin; Jason M Ridlon
Journal:  J Biol Chem       Date:  2019-06-17       Impact factor: 5.157

Review 9.  Conceptualizing the Vertebrate Sterolbiome.

Authors:  Jason M Ridlon
Journal:  Appl Environ Microbiol       Date:  2020-08-03       Impact factor: 4.792

10.  11-Oxygenated androgen precursors are the preferred substrates for aldo-keto reductase 1C3 (AKR1C3): Implications for castration resistant prostate cancer.

Authors:  Monique Barnard; Jonathan L Quanson; Elahe Mostaghel; Elzette Pretorius; Jacky L Snoep; Karl-Heinz Storbeck
Journal:  J Steroid Biochem Mol Biol       Date:  2018-06-21       Impact factor: 4.292

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