In situ metabolomics of aldosterone-producing adenomas.

Abstract

Recent genetic examinations and multisteroid profiles have provided the basis for subclassification of aldosterone-producing adenomas (APAs). The objective of the current study was to produce a comprehensive, high-resolution mass spectrometry imaging (MSI) map of APAs in relation to morphometry, immunohistochemical profiles, mutational status, and clinical outcome. The study cohort comprised 136 patients with unilateral primary aldosteronism. Matrix-assisted laser desorption/ionization-Fourier transform-ion cyclotron resonance MSI was conducted, and metabolite profiles were analyzed with genotype/phenotype information, including digital image analysis from morphometry and IHC of steroidogenic enzymes. Distinct molecular signatures between KCNJ5- and CACNA1D-mutated APAs with significant differences of 137 metabolites, including metabolites of purine metabolism and steroidogenesis, were observed. Intratumor concentration of 18-oxocortisol and 18-hydroxycortisol were inversely correlated with the staining intensity of CYP11B1. Lower staining intensity of CYP11B1 and higher levels of 18-oxocortisol were associated with a higher probability of complete clinical success after surgery. The present study demonstrates distinct metabolomic profiles of APAs in relation to tumor genotype. In addition, we reveal an inverse correlation between cortisol derivatives and CYP11B1 and the impact of 18-oxocortisol and CYP11B1 on clinical outcome, which provides unprecedented insights into the pathophysiology, clinical features, and steroidogenesis of APAs.

• Authors: Masanori Murakami, Yara Rhayem, Thomas Kunzke, Na Sun, Annette Feuchtinger, Philippe Ludwig, Tim Matthias Strom, Celso Gomez-Sanchez, Thomas Knösel, Thomas Kirchner, Tracy Ann Williams, Martin Reincke, Axel Karl Walch, Felix Beuschlein
• Journal: JCI insight (JCI Insight) Vol. 4 Issue 17 (09 05 2019) ISSN: 2379-3708 [Electronic] United States
• PMID: 31484828 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)

Chemical References

• CACNA1D protein, human
• Calcium Channels, L-Type
• G Protein-Coupled Inwardly-Rectifying Potassium Channels
• KCNJ5 protein, human
• 18-oxocortisol
• Aldosterone
• Steroid 11-beta-Hydroxylase
• 18-hydroxycortisol
• Hydrocortisone

Topics

• Adenoma (genetics, metabolism)
• Adrenal Cortex Neoplasms (genetics, metabolism, pathology)
• Adrenocortical Adenoma (genetics, metabolism, pathology)
• Adult
• Aldosterone (genetics, metabolism)
• Calcium Channels, L-Type (metabolism)
• Cohort Studies
• Female
• G Protein-Coupled Inwardly-Rectifying Potassium Channels (metabolism)
• Genotype
• Humans
• Hydrocortisone (analogs & derivatives, metabolism)
• Hyperaldosteronism (metabolism)
• Male
• Metabolomics (methods)
• Middle Aged
• Mutation
• Phenotype
• Steroid 11-beta-Hydroxylase (metabolism)