collection
https://read.qxmd.com/read/34711511/rare-forms-of-genetic-steroidogenic-defects-affecting-the-gonads-and-adrenals
#1
REVIEW
Claudia Boettcher, Christa E Flück
Pathogenic variants have been found in all genes involved in the classic pathways of human adrenal and gonadal steroidogenesis. Depending on their function and severity, they cause characteristic disorders of corticosteroid and/or sex hormone deficiency, may result in atypical sex development at birth and/or puberty, and mostly lead to sexual dysfunction and infertility. Genetic disorders of steroidogenesis are all inherited in an autosomal recessive fashion. Loss of function mutations lead to typical phenotypes, while variants with partial activity may manifest with milder, non-classic, late-onset disorders that share similar phenotypes...
January 2022: Best Practice & Research. Clinical Endocrinology & Metabolism
https://read.qxmd.com/read/28274349/sex-hormones-and-acne
#2
JOURNAL ARTICLE
Qiang Ju, Tao Tao, Tingting Hu, Ayşe Serap Karadağ, Safaa Al-Khuzaei, WenChieh Chen
The skin is an endocrine organ with the expression of metabolizing enzymes and hormone receptors for diverse hormones. The sebaceous gland is the main site of hormone biosynthesis, especially for androgens, and acne is the classical androgen-mediated dermatosis. In sebocytes, conversion of 17-hydroxyprogesterone directly to dihydrotestosterone bypassing testosterone has been demonstrated, while type II 17β-hydroxysteroid dehydrogenase can inactivate the action of testosterone and dihydrotestosterone. The androgen receptor-dependent genomic effect of dihydrotestosterone on sebocytes is confirmed...
March 2017: Clinics in Dermatology
https://read.qxmd.com/read/28188242/steroid-hormone-analysis-in-diagnosis-and-treatment-of-dsd-position-paper-of-eu-cost-action-bm-1303-dsdnet
#3
REVIEW
A Kulle, N Krone, P M Holterhus, G Schuler, R F Greaves, A Juul, Y B de Rijke, M F Hartmann, A Saba, O Hiort, S A Wudy
Disorders or differences in sex development (DSD) comprise a heterogeneous group of conditions with an atypical sex development. For optimal diagnosis, highly specialised laboratory analyses are required across European countries. Working group 3 of EU COST (European Cooperation in Science and Technology) Action BM 1303 'DSDnet' 'Harmonisation of Laboratory Assessment' has developed recommendations on laboratory assessment for DSD regarding the use of technologies and analytes to be investigated. This position paper on steroid hormone analysis in diagnosis and treatment of DSD was compiled by a group of specialists in DSD and/or hormonal analysis, either from participating European countries or international partner countries...
May 2017: European Journal of Endocrinology
https://read.qxmd.com/read/28234803/clinical-significance-of-11-oxygenated-androgens
#4
JOURNAL ARTICLE
Adina F Turcu, Richard J Auchus
PURPOSE OF REVIEW: The adrenal gland is considered a source of weak androgens, such as dehydroepiandrosterone, dehydroepiandrosterone sulfate, and androstenedione. Emerging evidence proposes a set of 11-oxygenated 19-carbon (11oxC19) adrenal-derived steroids as clinically important androgens. Such steroids include 11β-hydroxyandrostenedione, 11-ketoandrostenedione, 11β-hydroxytestosterone, and 11-ketotestosterone. The present review will discuss the synthesis, androgenic activity, and clinical implications of the 11oxC19 steroids...
June 2017: Current Opinion in Endocrinology, Diabetes, and Obesity
https://read.qxmd.com/read/27489549/role-of-acth-in-the-interactive-paracrine-regulation-of-adrenal-steroid-secretion-in-physiological-and-pathophysiological-conditions
#5
REVIEW
Hervé Lefebvre, Michaël Thomas, Céline Duparc, Jérôme Bertherat, Estelle Louiset
In the normal human adrenal gland, steroid secretion is regulated by a complex network of autocrine/paracrine interactions involving bioactive signals released by endothelial cells, nerve terminals, chromaffin cells, immunocompetent cells, and adrenocortical cells themselves. ACTH can be locally produced by medullary chromaffin cells and is, therefore, a major mediator of the corticomedullary functional interplay. Plasma ACTH also triggers the release of angiogenic and vasoactive agents from adrenocortical cells and adrenal mast cells and, thus, indirectly regulates steroid production through modulation of the adrenal blood flow...
2016: Frontiers in Endocrinology
https://read.qxmd.com/read/27499746/aldo-keto-reductases-1b-in-adrenal-cortex-physiology
#6
REVIEW
Emilie Pastel, Jean-Christophe Pointud, Antoine Martinez, A Marie Lefrançois-Martinez
Aldose reductase (AKR1B) proteins are monomeric enzymes, belonging to the aldo-keto reductase (AKR) superfamily. They perform oxidoreduction of carbonyl groups from a wide variety of substrates, such as aliphatic and aromatic aldehydes or ketones. Due to the involvement of human aldose reductases in pathologies, such as diabetic complications and cancer, AKR1B subgroup enzymatic properties have been extensively characterized. However, the issue of AKR1B function in non-pathologic conditions remains poorly resolved...
2016: Frontiers in Endocrinology
https://read.qxmd.com/read/27524977/adrenal-mitochondria-and-steroidogenesis-from-individual-proteins-to-functional-protein-assemblies
#7
REVIEW
Andrew Midzak, Vassilios Papadopoulos
The adrenal cortex is critical for physiological function as the central site of glucocorticoid and mineralocorticoid synthesis. It possesses a great degree of specialized compartmentalization at multiple hierarchical levels, ranging from the tissue down to the molecular levels. In this paper, we discuss this functionalization, beginning with the tissue zonation of the adrenal cortex and how this impacts steroidogenic output. We then discuss the cellular biology of steroidogenesis, placing special emphasis on the mitochondria...
2016: Frontiers in Endocrinology
https://read.qxmd.com/read/26792828/60-years-of-pomc-transcriptional-and-epigenetic-regulation-of-pomc-gene-expression
#8
REVIEW
Jacques Drouin
Expression of the pro-opiomelanocortin (POMC) gene integrates numerous inputs that reflect the developmental history of POMC-expressing cells of the pituitary and hypothalamus, as well as their critical role in the endocrine system. These inputs are integrated at specific regulatory sequences within the promoter and pituitary or hypothalamic enhancers of the POMC locus. Investigations of developmental mechanisms and transcription factors (TFs) responsible for pituitary activation of POMC transcription led to the discovery of the Pitx factors that have critical roles in pituitary development and striking patterning functions in embryonic development...
May 2016: Journal of Molecular Endocrinology
https://read.qxmd.com/read/26792827/60-years-of-pomc-melanocortin-receptors-evolution-of-ligand-selectivity-for-melanocortin-peptides
#9
REVIEW
Robert M Dores, Liang Liang, Perry Davis, Alexa L Thomas, Bogdana Petko
The evolution of the melanocortin receptors (MCRs) is linked to the evolution of adrenocorticotrophic hormone (ACTH), the melanocyte-stimulating hormones (MSHs), and their common precursor pro-opiomelanocortin (POMC). The origin of the MCRs and POMC appears to be grounded in the early radiation of the ancestral protochordates. During the genome duplications that have occurred during the evolution of the chordates, the organization plan for POMC was established, and features that have been retained include, the high conservation of the amino acid sequences of α-MSH and ACTH, and the presence of the HFRW MCR activation motif in all of the melanocortin peptides (i...
May 2016: Journal of Molecular Endocrinology
https://read.qxmd.com/read/26762158/60-years-of-pomc-from-the-prohormone-theory-to-pro-opiomelanocortin-and-to-proprotein-convertases-pcsk1-to-pcsk9
#10
REVIEW
Michel Chrétien, Majambu Mbikay
Pro-opiomelanocortin (POMC), is a polyprotein expressed in the pituitary and the brain where it is proteolytically processed into peptide hormones and neuropeptides with distinct biological activities. It is the prototype of multipotent prohormones. The prohormone theory was first suggested in 1967 when Chrétien and Li discovered γ-lipotropin and observed that (i) it was part of β-lipotropin (β-LPH), a larger polypeptide characterized 2 years earlier and (ii) its C-terminus was β-melanocyte-stimulating hormone (β-MSH)...
May 2016: Journal of Molecular Endocrinology
https://read.qxmd.com/read/26759392/60-years-of-pomc-n-terminal-pomc-peptides-and-adrenal-growth
#11
REVIEW
Andrew B Bicknell
The peptide hormones contained within the sequence of proopiomelanocortin (POMC) have diverse roles ranging from pigmentation to regulation of adrenal function to control of our appetite. It is generally acknowledged to be the archetypal hormone precursor, and as its biology has been unravelled, so too have many of the basic principles of hormone biosynthesis and processing. This short review focuses on one group of its peptide products, namely, those derived from the N-terminal of POMC and their role in the regulation of adrenal growth...
May 2016: Journal of Molecular Endocrinology
https://read.qxmd.com/read/26793988/60-years-of-pomc-adrenal-and-extra-adrenal-functions-of-acth
#12
REVIEW
Nicole Gallo-Payet
The pituitary adrenocorticotropic hormone (ACTH) plays a pivotal role in homeostasis and stress response and is thus the major component of the hypothalamo-pituitary-adrenal axis. After a brief summary of ACTH production from proopiomelanocortin (POMC) and on ACTH receptor properties, the first part of the review covers the role of ACTH in steroidogenesis and steroid secretion. We highlight the mechanisms explaining the differential acute vs chronic effects of ACTH on aldosterone and glucocorticoid secretion...
May 2016: Journal of Molecular Endocrinology
https://read.qxmd.com/read/26908835/novel-mechanisms-for-dhea-action
#13
REVIEW
Russell A Prough, Barbara J Clark, Carolyn M Klinge
Dehydroepiandrosterone (3β-hydroxy-5-androsten-17-one, DHEA), secreted by the adrenal cortex, gastrointestinal tract, gonads, and brain, and its sulfated metabolite DHEA-S are the most abundant endogeneous circulating steroid hormones. DHEA actions are classically associated with age-related changes in cardiovascular tissues, female fertility, metabolism, and neuronal/CNS functions. Early work on DHEA action focused on the metabolism to more potent sex hormones, testosterone and estradiol, and the subsequent effect on the activation of the androgen and estrogen steroid receptors...
April 2016: Journal of Molecular Endocrinology
https://read.qxmd.com/read/26960203/disorders-in-the-initial-steps-of-steroid-hormone-synthesis
#14
REVIEW
Walter L Miller
Steroidogenesis begins with cellular internalization of low-density lipoprotein particles and subsequent intracellular processing of cholesterol. Disorders in these steps include Adrenoleukodystrophy, Wolman Disease and its milder variant Cholesterol Ester Storage Disease, and Niemann-Pick Type C Disease, all of which may present with adrenal insufficiency. The means by which cholesterol is directed to steroidogenic mitochondria remains incompletely understood. Once cholesterol reaches the outer mitochondrial membrane, its delivery to the inner mitochondrial membrane is regulated by the steroidogenic acute regulatory protein (StAR)...
January 2017: Journal of Steroid Biochemistry and Molecular Biology
https://read.qxmd.com/read/27761789/skin-steroidogenesis-in-health-and-disease
#15
REVIEW
Georgios Nikolakis, Constantine A Stratakis, Theodora Kanaki, Andrej Slominski, Christos C Zouboulis
The skin is an important extra-gonadal steroidogenic organ, capable of metabolizing various hormones from their precursors, as well as of synthesizing de novo a broad palette of sex steroids and glucocorticoids from cholesterol. In this manuscript, we review the major steroidogenic properties of human skin and we suggest steroidogenesis' impairment as a cardinal factor for various pathological conditions such as acne, rosacea, atopic dermatitis, and androgenic alopecia.
September 2016: Reviews in Endocrine & Metabolic Disorders
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