Hitit medical journal (Online), cilt.6, sa.3, ss.246-256, 2024 (Hakemli Dergi)
Objective: Autophagy plays a significant role in breast cancer tumorigenesis, including triple-negative breast cancer. Research indicates that hydroxychloroquine and thymoquinone modulate autophagy, potentially suppressing its activity. However, their combined effects on autophagy in triple-negative breast cancer remain unexplored. In this study, we investigated the potential anti-cancer and autophagy-modulating effects of hydroxychloroquine-thymoquinone combination on triple-negative breast cancer cells in vitro.
Material and Method: The viability of MDA-MB-231 cells was evaluated after treatment with hydroxychloroquine (10-210 µM) and thymoquinone (5-45 µM) for 24 and 48 hours using the WST-1 assay. Combination effects were analyzed using the Chou-Talalay method with CompuSyn (v.10). Autophagic vesicles were visualized using an Autophagy Detection Kit and fluorescence microscopy to investigate their role in the decrease in cell viability. Statistical analysis was performed with GraphPad Prism (v.8.3.0).
Results: At both 24- and 48-hour intervals post-treatment, a significant decrease in viability was observed for both hydroxychloroquine and thymoquinone treatments individually (p<0.0001). The combination of these drugs revealed pronounced synergistic effects at 24 hours, whereas antagonistic effects were noted at 48 hours (combination index>1). At 24 hours, favorable dose reduction effects were evident (dose reduction index >1), while the 48-hour results showed an unfavorable reduction (dose reduction index<1). Consequently, the 24-hour synergistic effects resulted in a reduction in autophagic vesicles (p<0.0001).(p<0.0001).
Conclusion: This study revealed, for the first time, a time-dependent decrease in triple-negative breast cancer cell viability via the autophagy mechanism induced by hydroxychloroquine and thymoquinone, highlighting their novel implications for triple-negative breast cancer treatment and autophagy modulation.