用于催化放射增敏的葡萄糖氧化酶和 MnO2 功能化脂质体增强了乳腺癌的协同治疗。

Lihua Shao, Dun Liu, Xuexue Liu, Xueyuan Wang, Xian Yang, Runyan Niu, Shaoping Yin, Peipei Xu, Yonghuan Mao, Xiao Du, Lin Yang
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引用次数: 0

摘要

近年来,放疗与纳米催化医学的结合在乳腺癌治疗中受到广泛关注。本文构建了葡萄糖氧化酶(GOx)和二氧化锰(MnO2)纳米颗粒共同修饰的多功能脂质体GOx-MnO2@Lip,用于增强放射治疗。引入 GOx 不仅会增加葡萄糖的消耗,使癌细胞处于饥饿状态,还会提高内源性 H2O2 的水平。同时,高浓度的细胞内 GSH 可促进 Mn2+ 的释放,通过肿瘤微环境中的级联催化反应放大细胞毒性-OH,使肿瘤抑制率达到 74.45%。此外,血液生化和血常规表明,GOx-MnO2@Lip 没有明显的毒副作用。因此,这项工作为协同癌症饥饿疗法、化学动力学疗法和放射疗法提高乳腺癌疗效提供了潜在的载体。
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Glucose oxidase and MnO2 functionalized liposome for catalytic radiosensitization enhanced synergistic breast cancer therapy.

In recent years, the integration of radiotherapy and nanocatalytic medicine has gained widespread attention in the treatment of breast cancer. Herein, the glucose oxidase (GOx) and MnO2 nanoparticles co-modified multifunctional liposome of GOx-MnO2@Lip was constructed for enhanced radiotherapy. Introduction of GOx would not only elevate the glucose consumption to starve the cancer cells, but also increased the endogenous H2O2 level. Meanwhile, high intracellular GSH concentration facilitated the release of Mn2+ to amplify the cytotoxic ·OH through cascade catalytic reactions within the tumor microenvironment, resulting in a favorable tumor suppression rate of 74.45 %. Furthermore, the blood biochemical and blood routine demonstrated that GOx-MnO2@Lip had no obvious toxic side effects. Therefore, this work provided a potential vehicle for synergistic cancer starving therapy, chemodynamic therapy and radiotherapy for improving therapeutic efficacy of breast cancer.

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