Department of Ultrasound & Laboratory of Translational Research in Ultrasound Theranostics, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, Affiliated Cancer Hospital of University of Electronic Science and Technology of China, Chengdu 610042, China.
Department of Radiology, Center for Medical Imaging, and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu 610044, China.
ACS Nano. 2024 Oct 22;18(42):29121-29139. doi: 10.1021/acsnano.4c10603. Epub 2024 Oct 10.
Microwave thermotherapy (MT) is a clinical local tumor ablation modality, but its applications are limited by its therapeutic efficacy and safety. Therefore, developing sensitizers to optimize the outcomes of MT is in demand in clinical practice. Herein, we engineered a special nanoframework (i.e., FdMI) based on a fucoidan-decorated zirconium metal-organic framework incorporating manganese ions and liquid physisorption for microwave tumor ablation. The monodisperse nanoframework exhibited both microwave thermal effects and microwave dynamic effects, which could effectively kill cancer cells by efficient intracellular drug delivery. Through fucoidan-mediated targeting of P-selectin in the tumor microenvironment (TME), the FdMI effectively accumulated in tumor regions, leading to significant eradication of orthotropic triple-negative breast cancer (TNBC) and aggressive Hepa1-6 liver tumors by the synergistic effects of microwave thermotherapy/dynamic therapy (MT/MDT). The eradication of primary tumors could activate systemic immune responses, which effectively inhibited distant TNBC tumors and lung metastasis of Hepa1-6 liver tumors, respectively. This work not only engineered nanoparticle sensitizers for tumor-targeted synergistic MT/MDT but also demonstrated that nanocarrier-based microwave tumor ablation could stimulate antitumor immunity to effectively inhibit distant and metastatic tumors, demonstrating the high potential for effectively managing advanced malignant tumors.
微波热疗(MT)是一种临床局部肿瘤消融方式,但由于其治疗效果和安全性的限制,其应用受到限制。因此,在临床实践中需要开发敏化剂来优化 MT 的治疗效果。在此,我们基于一种具有锰离子和液相物理吸附功能的壳聚糖修饰的锆基金属有机骨架,构建了一种特殊的纳米框架(即 FdMI),用于微波肿瘤消融。该单分散纳米框架表现出微波热效应和微波动力学效应,通过有效的细胞内药物传递,能够有效杀死癌细胞。通过肿瘤微环境(TME)中 P-选择素介导的壳聚糖靶向作用,FdMI 能够有效地在肿瘤区域聚集,从而通过微波热疗/动力学治疗(MT/MDT)的协同作用,显著消除原位三阴性乳腺癌(TNBC)和侵袭性 Hepa1-6 肝癌。原发肿瘤的消除能够激活全身免疫反应,分别有效地抑制远处 TNBC 肿瘤和 Hepa1-6 肝癌的肺转移。这项工作不仅为肿瘤靶向协同 MT/MDT 设计了纳米颗粒敏化剂,还证明了基于纳米载体的微波肿瘤消融能够刺激抗肿瘤免疫,有效地抑制远处和转移性肿瘤,为有效治疗晚期恶性肿瘤提供了广阔的前景。