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

Endocrine reviews, 2019-04, Vol.40 (2), p.447-475

2019

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Role of aldo–keto reductase family 1 (AKR1) enzymes in human steroid metabolism

Steroids, 2014-01, Vol.79, p.49-63

2014

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Conversion of Classical and 11-Oxygenated Androgens by Insulin-Induced AKR1C3 in a Model of Human PCOS Adipocytes

Endocrinology (Philadelphia), 2022-07, Vol.163 (7), p.1

2022

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Steroid Hormone Transforming Aldo-Keto Reductases and Cancer

Annals of the New York Academy of Sciences, 2009-02, Vol.1155 (1), p.33-42

2009

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Mechanisms of activation of the transcription factor Nrf2 by redox stressors, nutrient cues, and energy status and the pathways through which it attenuates degenerative disease

Free radical biology & medicine, 2015-11, Vol.88 (Pt B), p.108-146

2015

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Insulin-Induced AKR1C3 Induces Fatty Acid Synthase in a Model of Human PCOS Adipocytes

Endocrinology (Philadelphia), 2023-03, Vol.164 (5)

2023

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Letter to the Editor From Penning and Detlefsen “Hydroxyeicosatetraenoic Acid Controls Androgen Reduction in Diverse Types of Human Epithelial Cells”

Endocrinology (Philadelphia), 2023-05, Vol.164 (5), p.1

2023

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Aldo-keto reductase 1C3—Assessment as a new target for the treatment of endometriosis

Pharmacological research, 2020-02, Vol.152, p.104446, Article 104446

2020

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Unique patterns of molecular profiling between human prostate cancer LNCaP and PC-3 cells

The Prostate, 2009-07, Vol.69 (10), p.1077-1090

2009

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Transcript Profiling of the Androgen Signal in Normal Prostate, Benign Prostatic Hyperplasia, and Prostate Cancer

Endocrinology (Philadelphia), 2006-12, Vol.147 (12), p.5806-5816

2006

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Insulin Signaling Induces AKR1C3 to Promote Lipid Overload through FASN in SGBS Cells, as a Model of PCOS Adipocytes

The FASEB journal, 2022-05, Vol.36 (S1), p.n/a

2022

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5β-Reduced steroids and human Δ(4)-3-ketosteroid 5β-reductase (AKR1D1)

Steroids, 2014-05, Vol.83, p.17

2014

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Exposure to Ambient Particulate Matter Is Associated With Accelerated Functional Decline in Idiopathic Pulmonary Fibrosis

Chest, 2018-05, Vol.153 (5), p.1221-1228

2018

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A new nomenclature for the aldo-keto reductase superfamily

Biochemical pharmacology, 1997-09, Vol.54 (6), p.639-647

1997

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Characterization of a monoclonal antibody for human aldo-keto reductase AKR1C3 (type 2 3α-hydroxysteroid dehydrogenase/type 5 17β-hydroxysteroid dehydrogenase); immunohistochemical detection in breast and prostate

Steroids, 2004-12, Vol.69 (13), p.795-801

2004

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Characterization of the cancer chemopreventive NRF2-dependent gene battery in human keratinocytes: demonstration that the KEAP1–NRF2 pathway, and not the BACH1–NRF2 pathway, controls cytoprotection against electrophiles as well as redox-cycling compounds

Carcinogenesis (New York), 2009-09, Vol.30 (9), p.1571-1580

2009

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An indomethacin analogue, N-(4-chlorobenzoyl)-melatonin, is a selective inhibitor of aldo-keto reductase 1C3 (type 2 3α-HSD, type 5 17β-HSD, and prostaglandin F synthase), a potential target for the treatment of hormone dependent and hormone independent malignancies

Biochemical pharmacology, 2008-01, Vol.75 (2), p.484-493

2008

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New frontiers in androgen biosynthesis and metabolism

Current opinion in endocrinology, diabetes, and obesity, 2010-06, Vol.17 (3), p.233-239

Penning, Trevor M

2010

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Current advances in intratumoral androgen metabolism in castration-resistant prostate cancer

Current opinion in endocrinology, diabetes, and obesity, 2016-06, Vol.23 (3), p.264-270

2016

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Hydroxysteroid dehydrogenases and pre‐receptor regulation of steroid hormone action

Human reproduction update, 2003-05, Vol.9 (3), p.193-205

Penning, Trevor M

2003

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Substrate specificity and inhibitor analyses of human steroid 5β-reductase (AKR1D1)

Steroids, 2011-04, Vol.76 (5), p.484-490

2011

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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

Molecular endocrinology (Baltimore, Md.), 2006-02, Vol.20 (2), p.444-458

2006

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The Biochemical Basis for Increased Testosterone Production in Theca Cells Propagated from Patients with Polycystic Ovary Syndrome

The journal of clinical endocrinology and metabolism, 2001-12, Vol.86 (12), p.5925-5933

2001

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Human Type 3 3α-Hydroxysteroid Dehydrogenase (Aldo-Keto Reductase 1C2) and Androgen Metabolism in Prostate Cells

Endocrinology (Philadelphia), 2003-07, Vol.144 (7), p.2922-2932

2003

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

Role of aldo–keto reductase family 1 (AKR1) enzymes in human steroid metabolism

Conversion of Classical and 11-Oxygenated Androgens by Insulin-Induced AKR1C3 in a Model of Human PCOS Adipocytes

Steroid Hormone Transforming Aldo-Keto Reductases and Cancer

Mechanisms of activation of the transcription factor Nrf2 by redox stressors, nutrient cues, and energy status and the pathways through which it attenuates degenerative disease

Insulin-Induced AKR1C3 Induces Fatty Acid Synthase in a Model of Human PCOS Adipocytes

Letter to the Editor From Penning and Detlefsen “Hydroxyeicosatetraenoic Acid Controls Androgen Reduction in Diverse Types of Human Epithelial Cells”

Aldo-keto reductase 1C3—Assessment as a new target for the treatment of endometriosis

Unique patterns of molecular profiling between human prostate cancer LNCaP and PC-3 cells

Transcript Profiling of the Androgen Signal in Normal Prostate, Benign Prostatic Hyperplasia, and Prostate Cancer

Insulin Signaling Induces AKR1C3 to Promote Lipid Overload through FASN in SGBS Cells, as a Model of PCOS Adipocytes

5β-Reduced steroids and human Δ(4)-3-ketosteroid 5β-reductase (AKR1D1)

Exposure to Ambient Particulate Matter Is Associated With Accelerated Functional Decline in Idiopathic Pulmonary Fibrosis

A new nomenclature for the aldo-keto reductase superfamily

Characterization of a monoclonal antibody for human aldo-keto reductase AKR1C3 (type 2 3α-hydroxysteroid dehydrogenase/type 5 17β-hydroxysteroid dehydrogenase); immunohistochemical detection in breast and prostate

Characterization of the cancer chemopreventive NRF2-dependent gene battery in human keratinocytes: demonstration that the KEAP1–NRF2 pathway, and not the BACH1–NRF2 pathway, controls cytoprotection against electrophiles as well as redox-cycling compounds

Intense androgen-deprivation therapy with abiraterone acetate plus leuprolide acetate in patients with localized high-risk prostate cancer: results of a randomized phase II neoadjuvant study

An indomethacin analogue, N-(4-chlorobenzoyl)-melatonin, is a selective inhibitor of aldo-keto reductase 1C3 (type 2 3α-HSD, type 5 17β-HSD, and prostaglandin F synthase), a potential target for the treatment of hormone dependent and hormone independent malignancies

New frontiers in androgen biosynthesis and metabolism

Current advances in intratumoral androgen metabolism in castration-resistant prostate cancer

Hydroxysteroid dehydrogenases and pre‐receptor regulation of steroid hormone action

Substrate specificity and inhibitor analyses of human steroid 5β-reductase (AKR1D1)

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

The Biochemical Basis for Increased Testosterone Production in Theca Cells Propagated from Patients with Polycystic Ovary Syndrome

Human Type 3 3α-Hydroxysteroid Dehydrogenase (Aldo-Keto Reductase 1C2) and Androgen Metabolism in Prostate Cells

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