Journal Article Epublish
PubMed: 40371342 DOI: 10.3389/fphar.2025.1549288
Antibacterial activity of tamoxifen derivatives against methicillin-resistant Staphylococcus aureus.
Front Pharmacol 16:1549288
Authors: Irene Molina Panadero, Javier Falcón Torres, Abdelkrim Hmadcha, Salvatore Princiotto, Luigi Cutarella, Mattia Mori, Sabrina Dallavalle, Michael S Christodoulou, Younes Smani
Affiliations
- Andalusian Center of Developmental Biology, Consejo Superior de Investigaciones Científicas (CSIC), University of Pablo de Olavide - Seville, Seville, Spain.
- Department of Molecular Biology and Biochemical Engineering, University of Pablo de Olavide, Seville, Spain.
- Biosanitary Research Institute (IIB-VIU), Valencian International University (VIU), Valencia, Spain.
- Department of Food, Environmental and Nutritional Sciences (DeFENS), University of Milan, Milan, Italy.
- Department f Biotechnology, Chemistry and Pharmacy, University of Siena, Siena, Italy.
Abstract
The development of new antimicrobial therapeutic strategies requires urgent attention to prevent the tens of millions of deaths predicted to occur by 2050 as a result of multidrug-resistant (MDR) bacterial infections. This study aimed to discover new tamoxifen derivatives with antimicrobial potential, particularly targeting methicillin-resistant Staphylococcus aureus (MRSA). The minimum inhibitory concentration (MIC) of 22 tamoxifen derivatives was determined against S. aureus reference and MRSA strains using microdilution assays. The antibacterial effects of selected tamoxifen derivatives against MRSA (USA7 strain) were assessed through bacterial growth assays. Additionally, bacterial membrane permeability and molecular dynamics (MD) simulation assays were performed. The MIC of the tamoxifen derivatives against reference S. aureus and MRSA strains ranged from to 16 to >64 μg/mL. Bacterial growth assays demonstrated that tamoxifen derivatives 2, 5, and 6, the only compounds bearing the electron-donating hydroxyl group in the para position on both phenyl rings of the tamoxifen skeleton, dose-dependently reduced the growth of the USA7 strain. Moreover, treatment of MRSA with derivatives 2 and 5 resulted in a slight increase of membrane permeabilization. Extensive MD simulations on the interaction between 5 and 6 and the S. aureus membrane model suggest that the compounds do not act by destabilizing the membrane integrity. These findings suggest that tamoxifen derivatives exhibit antibacterial activity against MRSA, potentially broadening the spectrum of available drug treatments for combating antimicrobial-resistant S. aureus.
MeSH
Methicillin-Resistant Staphylococcus Aureus, Staphylococcus, Growth, Pharmaceutical Preparations, Transcutaneous Electric Nerve Stimulation, Staphylococcus Aureus, Therapeutics, Membranes, Methicillin, Infections, Tamoxifen