Deng Xi, Yang Zhongming, Chan Kim Wei, Abu Bakar Md Zuki
Natural Medicines and Products Research Laboratory, Institute of Bioscience, Universiti Putra Malaysia, Serdang 43400, Selangor, Malaysia.
Department of Veterinary Preclinical Science, Faculty of Veterinary Medicine, Universiti Putra Malaysia, Serdang 43400, Selangor, Malaysia.
Pharmaceutics. 2024 Jul 30;16(8):1011. doi: 10.3390/pharmaceutics16081011.
Given the need for novel and effective therapies for colon cancer, this study aimed to investigate the effects of 5-fluorouracil-loaded calcium carbonate nanoparticles (5FU-CaCOnp) combined with thymoquinone (TQ) against colon cancer. A shaking incubator and a high-speed homogenizer were used to prepare the optimal 5FU-CaCOnp, with characterizations of physicochemical properties, in vitro drug release profile, and biocompatibility. In vitro experiments and molecular docking were employed to evaluate the therapeutic potential of the combination for colon cancer treatment. Study results revealed that 5FU-CaCOnp with a size of approximately 130 nm was synthesized using the high-speed homogenizer. Its favorable biocompatibility, pH sensitivity, and sustained release properties facilitated reduced toxic side effects of 5-FU on NIH3T3 normal cells and enhanced inhibitory effects on CT26 colon cancer cells. The combination of 5FU-CaCOnp (1.875 μM) and TQ (30 μM) showed significantly superior anti-colon cancer effects to 5FU-CaCOnp alone in terms of cell proliferation and migration inhibition, cell apoptosis induction, and spheroid growth suppression in CT26 cells ( < 0.05), with strong interactions between the drugs and targets (E-cadherin, Bcl-2, PCNA, and MMP-2). These results provide evidence for 5FU-CaCOnp as a novel regimen against colon cancer. Combining 5FU-CaCOnp and TQ may offer a new perspective for colon cancer therapy.
鉴于结肠癌需要新颖有效的治疗方法,本研究旨在探讨负载5-氟尿嘧啶的碳酸钙纳米颗粒(5FU-CaCOnp)与百里醌(TQ)联合应用对结肠癌的影响。使用振荡培养箱和高速匀浆机制备最佳的5FU-CaCOnp,并对其理化性质、体外药物释放曲线和生物相容性进行表征。采用体外实验和分子对接来评估该联合用药对结肠癌治疗的潜在疗效。研究结果显示,使用高速匀浆机合成了尺寸约为130 nm的5FU-CaCOnp。其良好的生物相容性、pH敏感性和缓释特性有助于降低5-氟尿嘧啶对NIH3T3正常细胞的毒副作用,并增强对CT26结肠癌细胞的抑制作用。在CT26细胞的细胞增殖和迁移抑制、细胞凋亡诱导以及球体生长抑制方面,5FU-CaCOnp(1.875 μM)与TQ(30 μM)联合使用显示出比单独使用5FU-CaCOnp显著更优的抗结肠癌效果(<0.05),且药物与靶点(E-钙黏蛋白、Bcl-2、增殖细胞核抗原和基质金属蛋白酶-2)之间存在强烈相互作用。这些结果为5FU-CaCOnp作为一种新型抗结肠癌方案提供了证据。5FU-CaCOnp与TQ联合使用可能为结肠癌治疗提供新的视角。