Valsalakumari Remya, Feith Marek, Pettersen Solveig, Åslund Andreas K O, Mørch Ýrr, Skotland Tore, Sandvig Kirsten, Mælandsmo Gunhild Mari, Iversen Tore-Geir
Department of Tumor Biology, Institute for Cancer Research, Oslo University Hospital, 0379 Oslo, Norway.
Department of Molecular Cell Biology, Institute for Cancer Research, Oslo University Hospital, 0379 Oslo, Norway.
Pharmaceutics. 2025 May 17;17(5):657. doi: 10.3390/pharmaceutics17050657.
Combination therapies for cancer have gained considerable attention due to their potential for enhancing therapeutic efficacy and decreasing drug resistance. Introducing nanodrug delivery systems in this context may further improve the therapy due to targeted delivery, improved drug stability, sustained drug release, and prevention of rapid clearance from circulation. This study evaluates the combinatorial effects of two cytotoxic drugs, cabazitaxel (CBZ) and RSL3 (RAS-selective lethal 3), in free form as well as encapsulated within poly(2-ethyl butyl cyanoacrylate) (PEBCA) nanoparticles (NPs) in breast cancer cell lines. : Cell proliferation was assessed using IncuCyte technology, and synergistic drug effects were determined with SynergyFinder Plus. Cell viability was measured with the MTT assay. Additionally, we investigated whether the combinatorial effects were reflected in alterations of metabolic activity or reactive oxygen species (ROS) production using Seahorse technology and the CM-HDCFDA assay, respectively. : The data presented reveal, for the first time, that CBZ and RSL3 exhibit synergistically or additively combinatorial effects on various breast cancer cell lines. The pattern of cytotoxic effects was consistent, whether the drugs were in free form or encapsulated in NPs. Moreover, the combinatorial effects were not observed to be associated with early changes in metabolic activity or ROS production. : This study highlights the potential of CBZ and RSL3 in combinatorial nanomedicine as they may act synergistically. Further studies are warranted to better understand the mechanisms behind these combinatorial effects.
癌症联合疗法因其增强治疗效果和降低耐药性的潜力而备受关注。在这种情况下引入纳米药物递送系统可能会进一步改善治疗效果,因为其具有靶向递送、提高药物稳定性、持续药物释放以及防止药物从循环中快速清除的特点。本研究评估了两种细胞毒性药物,即游离形式的卡巴他赛(CBZ)和RSL3(RAS选择性致死3)以及封装在聚(2-乙基丁基氰基丙烯酸酯)(PEBCA)纳米颗粒(NPs)中的这两种药物在乳腺癌细胞系中的联合效应。使用IncuCyte技术评估细胞增殖,并使用SynergyFinder Plus确定药物协同效应。通过MTT法测量细胞活力。此外,我们分别使用Seahorse技术和CM-HDCFDA测定法研究联合效应是否反映在代谢活性改变或活性氧(ROS)产生上。所呈现的数据首次揭示,CBZ和RSL3对各种乳腺癌细胞系表现出协同或相加的联合效应。无论药物是游离形式还是封装在NPs中,细胞毒性作用模式都是一致的。此外,未观察到联合效应与代谢活性或ROS产生的早期变化有关。本研究突出了CBZ和RSL3在联合纳米医学中的潜力,因为它们可能具有协同作用。有必要进行进一步研究以更好地理解这些联合效应背后的机制。