Androgen production in pediatric adrenocortical tumors may occur via both the classic and/or the alternative backdoor pathway
Jazyk angličtina Země Irsko Médium print-electronic
Typ dokumentu kazuistiky, časopisecké články, práce podpořená grantem
PubMed
28501574
DOI
10.1016/j.mce.2017.05.014
PII: S0303-7207(17)30272-1
Knihovny.cz E-zdroje
- Klíčová slova
- Alternative (backdoor) pathway, Androgen biosynthesis, Classic pathway, Dihydrotestosterone, Pediatric adrenocortical tumors,
- MeSH
- adrenokortikální karcinom metabolismus patologie MeSH
- adrenokortikální nádory metabolismus patologie MeSH
- androgeny biosyntéza krev MeSH
- dihydrotestosteron krev MeSH
- dítě MeSH
- imunohistochemie MeSH
- kojenec MeSH
- lidé MeSH
- Liův-Fraumeniho syndrom genetika MeSH
- mladiství MeSH
- nádorový supresorový protein p53 genetika MeSH
- nádory vaječníků metabolismus patologie MeSH
- virilizace metabolismus patologie MeSH
- Check Tag
- dítě MeSH
- kojenec MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- práce podpořená grantem MeSH
- Názvy látek
- androgeny MeSH
- dihydrotestosteron MeSH
- nádorový supresorový protein p53 MeSH
- TP53 protein, human MeSH Prohlížeč
Children with adrenocortical tumors (ACTs) often present with virilization due to high tumoral androgen production, with dihydrotestosterone (DHT) as most potent androgen. Recent work revealed two pathways for DHT biosynthesis, the classic and the backdoor pathway. Usage of alternate routes for DHT production has been reported in castration-resistant prostate cancer, CAH and PCOS. To assess whether the backdoor pathway may contribute to the virilization of pediatric ACTs, we investigated seven children suffering from androgen producing tumors using steroid profiling and immunohistochemical expression studies. All cases produced large amounts of androgens of the classic and/or backdoor pathway. Variable expression of steroid enzymes was observed in carcinomas and adenomas. We found no discriminative pattern. This suggests that enhanced androgen production in pediatric ACTs is the result of deregulated steroidogenesis through multiple steroid pathways. Thus future treatments of ACTs targeting androgen overproduction should consider these novel steroid production pathways.
Institute of Pathology University of Bern Switzerland
Pediatric Endocrinology and Diabetology Department of Pediatrics Switzerland
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