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通过仿生矿化制备的纳米级双酶级联金属有机框架作为活性氧生成剂用于协同癌症治疗

Nanoscale dual-enzyme cascade metal-organic frameworks through biomimetic mineralization as ROS generators for synergistic cancer therapy.

作者信息

Jin Shuiling, Weng Lanling, Li Zhi, Yang Zhenzhen, Zhu Lili, Shi Jianxiang, Tang Wenxue, Ma Wang, Zong Hong, Jiang Wei

机构信息

Department of Oncology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, China.

出版信息

J Mater Chem B. 2020 Jun 7;8(21):4620-4626. doi: 10.1039/d0tb00357c. Epub 2020 May 6.

DOI:10.1039/d0tb00357c
PMID:32373876
Abstract

Chemodynamic therapy (CDT) has been critically challenged by insufficient HO in cancer tissues and inefficient reactive oxygen species (ROS) production. Herein, we have reported the facile synthesis of an efficient ROS generator (GOx@Pd@ZIF-8) that exerts synergistic anticancer activity by blocking glucose metabolism and producing ROS. Glucose oxidase (GOx) and palladium (Pd) cube nanozymes were incorporated in zeolitic imidazolate framework-8 (ZIF-8) by biomimetic mineralization. Systematic characterization indicated the successful entrapment and embedding of GOx and Pd during ZIF-8 crystal growth. The GOx@Pd@ZIF-8 composite showed favorable catalytic glucose activity and stable ROS production. In vitro experiments showed that the GOx@Pd@ZIF-8 composite effectively inhibited cancer cell proliferation, invasion, and migration and promoted apoptosis through the ROS-mediated signaling pathway, which was further confirmed by bioinformatics analyses of RNA-seq data obtained from in vitro experiments. Furthermore, the GOx@Pd@ZIF-8 composite inhibited tumor growth with few to no side effects on other tissues in vivo. This work provides a novel antitumor strategy involving the construction of a stable and highly active ROS generator that shows promise for the treatment of solid cancers.

摘要

化学动力疗法(CDT)因癌组织中过氧化氢(HO)不足以及活性氧(ROS)生成效率低下而受到严峻挑战。在此,我们报道了一种高效ROS发生器(GOx@Pd@ZIF-8)的简便合成方法,该发生器通过阻断葡萄糖代谢和产生活性氧发挥协同抗癌活性。葡萄糖氧化酶(GOx)和钯(Pd)立方纳米酶通过仿生矿化作用被包裹在沸石咪唑酯骨架-8(ZIF-8)中。系统表征表明在ZIF-8晶体生长过程中成功包埋和嵌入了GOx和Pd。GOx@Pd@ZIF-8复合材料表现出良好的催化葡萄糖活性和稳定的ROS生成。体外实验表明,GOx@Pd@ZIF-8复合材料通过ROS介导的信号通路有效抑制癌细胞增殖、侵袭和迁移,并促进细胞凋亡,这通过对体外实验获得的RNA测序数据进行生物信息学分析得到进一步证实。此外,GOx@Pd@ZIF-8复合材料在体内抑制肿瘤生长,对其他组织几乎没有副作用。这项工作提供了一种新的抗肿瘤策略,即构建一种稳定且高活性的ROS发生器,有望用于治疗实体癌。

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