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Androgen biosynthetic pathways in the human prostate
Abstract
It is well recognized that there are two androgens, namely testosterone (T) and dihydrotestosterone (DHT); T plays an important role in the testis and muscle, and DHT is crucial for the development, function and pathology of the prostate. It is generally thought that DHT is produced from the 5alpha-reduction of circulating T before being inactivated by 3alpha-hydroxysteroid dehydrogenase (3alpha-HSD) that converts DHT into 5alpha-androstane-3alpha,17beta-diol (3alpha-diol). However, the presence of various steroidogenic enzymes in the prostate as well as the availability at high levels of various steroid precursors such as dehydroepiandrosterone sulphate (DHEAS), dehydroepiandrosterone (DHEA) and 4-androstenedione (4-dione) strongly suggest the existence of additional pathways involved in the biosynthesis and metabolism of DHT. Because steroidogenesis could be different in different species, data from the literature obtained from various human, dog, rat and mouse prostate tissues, as well as primary cells and prostatic cancer cell lines, provide a somewhat confusing picture. In the present chapter, we review the data in order to provide a clearer picture of the pathways involved in DHT biosynthesis and metabolism in the human prostate.
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“numerous studies have shown that CRPC is dependent on the intracrine conversion of circulating androgen precursors of adrenal origin to active androgens reviewed in (Capper et al., 2016, Luu-The et al., 2008, Pretorius et al., 2017, Sharifi and Auchus, 2012).”
From Intracrine androgen biosynthesis, metabolism and action revisited (2018) · cites this paper as Luu-The et al., 2008
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- Robert A, Rheault P, Labrie F, et al. Identification and characterization of an estrogen-activating and androgen-inactivating (EHAL) enzyme. In: Breast Cancer Research National Scientific Conference, Reasons for Hope Abstract: 82; 1999.
- Robert A, Luu-The V. Cloning and characterization of a new form of human 3-keto-reductase specific for saturated steroid. In: CDA/CSEM Professional Conference and Annual Meetings, Ottawa; 1999.
- Mendonca, 1999, 17Beta-hydroxysteroid dehydrogenase 3 deficiency in women, The Journal of Clinical Endocrinology and Metabolism, 84, 802
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Metadata
- Authors
- Luu-The, V., Bélanger, A., & Labrie, F.
- Affiliations
- Université Laval (CA)
- Corresponding author
- Luu-The, Van
- Venue
- Best Practice & Research Clinical Endocrinology & Metabolism
- Publisher
- Elsevier BV
- Published
- 2008-04
- Volume
- 22
- Issue
- 2
- Pages
- 207-221
- ISSN
- 1521-690X (ISSN-L)
- OpenAlex
- W2007245161
- Cited by
- 169
- References
- 110
- Citations by year
- 2026: 3 · 2025: 1 · 2024: 1 · 2023: 5 · 2022: 9 · 2021: 5 · 2020: 1 · 2019: 11 · 2018: 9 · 2017: 8 · 2016: 11 · 2015: 9 · 2014: 9 · 2013: 16 · 2012: 18
- FWCI
- 2.85
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Best Practice & Research Clinical Endocrinology & Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Prostate Cancer Treatment and Research
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
- Health Sciences › Medicine › Reproductive Medicine › Sperm and Testicular Function
- Keywords
- androgen production, dihydrotestosterone, testosterone, human prostate, 5α-reduction, 3α-hydroxysteroid dehydrogenase, 3alpha-diol, dehydroepiandrosterone sulfate, dehydroepiandrosterone, 4-androstenedione, steroidogenic enzymes, prostate cancer
- MeSH terms
- Androgens, Animals, Humans, Hydroxysteroid Dehydrogenases, Male, Models, Biological, Oxidoreductases, Prostate, Dihydrotestosterone, Testosterone, Biosynthetic Pathways
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