Shenzhen Research Institute of Shandong University, Shenzhen, 518057, China.
Institute of Frontier Chemistry, School of Chemistry and Chemical Engineering, Shandong University, Qingdao, Shandong, 266237, China.
Adv Healthc Mater. 2024 Sep;13(23):e2400943. doi: 10.1002/adhm.202400943. Epub 2024 Jun 19.
Cancer cells support their uncontrolled proliferation primarily by regulating energy metabolism. Inhibiting tumor growth by blocking the supply of nutrients is an effective treatment strategy. Fasting-mimicking diet (FMD), as a low-calorie, low-protein, low-sugar, high-fat diet, can effectively reduce the nutrient supply to tumor cells. However, the significant biological barrier presented by the tumor microenvironment imposes greater demands and challenges for drug design. This study constructs the multifunctional nanocomposite ZnFeO@TiO@CHC@Orl-FA (ZTCOF), which has great potential to overcome the aforementioned drawbacks. ZnFeO@TiO could produce O with ultrasound, and stimulate the Fenton-like conversion of endogenous HO to ·OH, achieving a combined therapeutic effect of sonodynamic therapy (SDT) and chemodynamic therapy (CDT). Orl (Orlistat) and CHC (α-cyano-4-hydroxycinnamic acid) not only block tumor cell energy metabolism but also increase sensitivity to reactive oxygen species, enhancing the cytotoxic effect on tumor cells. Furthermore, combining the treatment strategies with FMD condition control can further inhibit cancer cell energy metabolism, achieving significant synergistic anti-tumor therapy. Both in vitro and in vivo experiments confirm that ZTCOF with SDT/CDT/starvation can achieve effective tumor suppression and destruction. This work provides theoretical and technical support for anti-tumor multimodal synergistic therapy.
癌细胞主要通过调节能量代谢来支持其不受控制的增殖。通过阻断营养供应来抑制肿瘤生长是一种有效的治疗策略。模拟禁食饮食(FMD)作为一种低热量、低蛋白、低糖、高脂肪的饮食,可以有效地减少肿瘤细胞的营养供应。然而,肿瘤微环境所带来的显著生物学屏障对药物设计提出了更高的要求和挑战。本研究构建了多功能纳米复合材料 ZnFeO@TiO@CHC@Orl-FA(ZTCOF),具有克服上述缺点的巨大潜力。ZnFeO@TiO 可以在超声下产生 O,刺激内源性 HO 的芬顿样转化为·OH,实现声动力治疗(SDT)和化学动力治疗(CDT)的联合治疗效果。Orl(奥利司他)和 CHC(α-氰基-4-羟基肉桂酸)不仅阻断肿瘤细胞的能量代谢,还增加了对活性氧的敏感性,增强了对肿瘤细胞的细胞毒性作用。此外,将治疗策略与 FMD 条件控制相结合可以进一步抑制肿瘤细胞的能量代谢,实现显著的协同抗肿瘤治疗效果。体外和体内实验均证实,具有 SDT/CDT/饥饿作用的 ZTCOF 可以实现有效的肿瘤抑制和破坏。这项工作为抗肿瘤多模态协同治疗提供了理论和技术支持。