Three-Dimensional Proteome-Wide Scale Screening for the 5‑Alpha Reductase Inhibitor Finasteride: Identification of a Novel Off-Target

• Published in: Journal of medicinal chemistry 2021-04, Vol.64 (8), p.4553-4566
• Main Authors: Giatti, Silvia, Di Domizio, Alessandro, Diviccaro, Silvia, Falvo, Eva, Caruso, Donatella, Contini, Alessandro, Melcangi, Roberto Cosimo
• Format: Article
• Language: English
• Subjects: 5-alpha Reductase Inhibitors - chemistry; 5-alpha Reductase Inhibitors - metabolism; 5-alpha Reductase Inhibitors - pharmacology; Animals; Binding Sites; Binding, Competitive; Catecholamines - analysis; Catecholamines - metabolism; Chromatography, High Pressure Liquid; Databases, Protein; Epinephrine - metabolism; Finasteride - chemistry; Finasteride - metabolism; Finasteride - pharmacology; Humans; Male; Molecular Docking Simulation; Molecular Dynamics Simulation; Phenylethanolamine N-Methyltransferase - chemistry; Phenylethanolamine N-Methyltransferase - metabolism; Protein Binding; Rats; Rats, Sprague-Dawley; Tandem Mass Spectrometry; Thermodynamics
• ISSN: 0022-2623; 1520-4804; 1520-4804
• DOI: 10.1021/acs.jmedchem.0c02039

Finasteride, a 5-alpha reductase (5α-R) inhibitor, is a widely used drug for treating androgen-dependent conditions. However, its use is associated with sexual, psychological, and physical complaints, suggesting that other mechanisms, in addition to 5α-R inhibition, may be involved. Here, a multidisciplinary approach has been used to identify potential finasteride off-target proteins. SPILLO-PBSS software suggests an additional inhibitory activity of finasteride on phenylethanolamine N-methyltransferase (PNMT), the limiting enzyme in formation of the stress hormone epinephrine. The interaction of finasteride with PNMT was supported by docking and molecular dynamics analysis and by in vitro assay, confirming the inhibitory nature of the binding. Finally, this inhibition was also confirmed in an in vivo rat model. Literature data indicate that PNMT activity perturbation may be correlated with sexual and psychological side effects. Therefore, results here obtained suggest that the binding of finasteride to PNMT might have a role in producing the side effects exerted by finasteride treatment.