Synergistic Anti-tumorigenic Effects of Cabazitaxel and Usnic Acid Combination on Metastatic Castration-Resistant Prostate Cancer Cells
- Authors: Bergel C.1, Eryilmaz I.E.1, Bulut E.1, Balaban R.1, Egeli U.1, Cecener G.1
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Affiliations:
- Department of Medical Biology, Faculty of Medicine, Bursa Uludag University
- Issue: Vol 25, No 9 (2025)
- Pages: 610-619
- Section: Chemistry
- URL: https://filvestnik.nvsu.ru/1871-5206/article/view/694517
- DOI: https://doi.org/10.2174/0118715206336754241015062614
- ID: 694517
Cite item
Full Text
Abstract
Background:Prostate cancer (PC) affects millions of men, causing high mortality rates. Despite the treatment approaches, the options for metastatic castration-resistant prostate cancer (mCRPC), a lethal form of advanced PC, are still limited. Cabazitaxel (Cbx) is the last taxane-derived chemotherapeutic approved for Docetaxel- resistant mCRPC patients. However, its effects are limited due to the activation of several pathways. Therefore, new approaches are needed to increase the efficacy of Cbx. Usnic acid (UA) is a natural product with wellknown anti-tumorigenic and synergistic effects with various chemotherapeutics. Although the cytotoxicity of UA and Cbx has been evaluated on mCRPC cells, the anti-tumorigenic effect of UA combination with any taxane has not been investigated yet. Thus, we aimed to evaluate the possible synergistic effect of Cbx+UA in mCRPC cells.
Methods:Cell viability and apoptosis were analyzed using WST-1 and Annexin-V. Morphological changes were visualized by fluorescent staining. Finally, cell cycle, mitochondrial health, and ROS levels were determined.
Results:Based on WST-1 results, 25 μM UA exhibited significant additive and synergistic effects with the use of Cbx. Annexin V and cell cycle results showed that UA significantly enhanced the Cbx efficacy at increasing doses compared to using only Cbx (**p<0.01). Moreover, combined treatment significantly increased ROS levels and mitochondrial membrane depolarization compared with Cbx alone (**p<0.01).
Conclusions:Thus, the results suggest that UA increased the anti-tumorigenic effects of Cbx on mCRPC cells by increasing apoptosis, causing an increase in intracellular ROS and disrupting mitochondrial health. Consequently, combining UA and Cbx offers a new combined therapeutic strategy for mCRPC treatment.
About the authors
Ceyda Bergel
Department of Medical Biology, Faculty of Medicine, Bursa Uludag University
Email: info@benthamscience.net
Isil Ezgi Eryilmaz
Department of Medical Biology, Faculty of Medicine, Bursa Uludag University
Author for correspondence.
Email: info@benthamscience.net
Ebrucan Bulut
Department of Medical Biology, Faculty of Medicine, Bursa Uludag University
Email: info@benthamscience.net
Rumeysa Balaban
Department of Medical Biology, Faculty of Medicine, Bursa Uludag University
Email: info@benthamscience.net
Unal Egeli
Department of Medical Biology, Faculty of Medicine, Bursa Uludag University
Email: info@benthamscience.net
Gulsah Cecener
Department of Medical Biology, Faculty of Medicine, Bursa Uludag University
Email: info@benthamscience.net
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