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用于多酶级联和增强型癌症化学动力疗法的pH敏感型葡萄糖氧化酶与血红素配位胶束

A pH-Sensitive Glucose Oxidase and Hemin Coordination Micelle for Multi-Enzyme Cascade and Amplified Cancer Chemodynamic Therapy.

作者信息

Jiang Zhen, Li Jiexin, Liu Gengqi, Qiu Qian, Zhang Jingyu, Hao Minchao, Ren He, Zhang Yumiao

机构信息

School of Chemical Engineering and Technology, Key Laboratory of Systems Bioengineering (Ministry of Education), Frontiers Science Center for Synthetic Biology (Ministry of Education), Tianjin University, Tianjin, 300350, P. R. China.

出版信息

Small. 2024 Dec;20(51):e2407674. doi: 10.1002/smll.202407674. Epub 2024 Oct 4.

Abstract

Chemodynamic therapy (CDT) is an emerging therapeutic paradigm for cancer treatment that utilizes reactive oxygen species (ROS) to induce apoptosis of cancer cells but few biomaterials have been developed to differentiate the cancer cells and normal cells to achieve precise and targeted CDT. Herein, a simple cascade enzyme system is developed, termed hemin-micelles-GOx, based on hemin and glucose oxidase (GOx)-encapsulated Pluronic F127 (F127) micelles with pH-sensitive enzymatic activities. Histidine-tagged GOx can be easily chelated to hemin-F127 micelles via the coordination of histidine and ferrous ions in the center of hemin by simple admixture in an aqueous solution. In tumor microenvironment (TME), hemin-micelles-GOx exhibits enhanced peroxidase (POD)-like activities to generate toxic hydroxyl radicals due to the acidic condition, whereas in normal cells the catalase (CAT)-like, but not POD-like activity is amplified, resulting in the elimination of hydrogen peroxide to generate oxygen. In a murine melanoma model, hemin-micelles-GOx significantly suppresses tumor growth, demonstrating its great potential as a pH-mediated enzymatic switch for tumor management by CDT.

摘要

化学动力疗法(CDT)是一种新兴的癌症治疗范式,它利用活性氧(ROS)诱导癌细胞凋亡,但目前很少有生物材料能够区分癌细胞和正常细胞以实现精确靶向的CDT。在此,基于血红素和包裹葡萄糖氧化酶(GOx)的具有pH敏感酶活性的泊洛沙姆F127(F127)胶束,开发了一种简单的级联酶系统,称为血红素-胶束-GOx。通过在水溶液中简单混合,带有组氨酸标签的GOx可以通过组氨酸与血红素中心的亚铁离子配位,轻松螯合到血红素-F127胶束上。在肿瘤微环境(TME)中,由于酸性条件,血红素-胶束-GOx表现出增强的过氧化物酶(POD)样活性以产生活性羟基自由基,而在正常细胞中,过氧化氢酶(CAT)样活性而非POD样活性被放大,导致过氧化氢被消除以产生氧气。在小鼠黑色素瘤模型中,血红素-胶束-GOx显著抑制肿瘤生长,证明其作为通过CDT进行肿瘤管理的pH介导酶开关具有巨大潜力。

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