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锰-沸石咪唑酯骨架纳米酶通过产生羟基自由基以及逆转肿瘤微环境来杀死肿瘤。

Mn-ZIF nanozymes kill tumors by generating hydroxyl radical as well as reversing the tumor microenvironment.

作者信息

Han Jiyu, Ma Hairong, Ai Songtao, Wan Daqian

机构信息

Department of Orthopedics, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.

Key Laboratory of Spine and Spinal Cord Injury Repair and Regeneration, Ministry of Education, Shanghai, China.

出版信息

Front Pharmacol. 2024 Aug 13;15:1441818. doi: 10.3389/fphar.2024.1441818. eCollection 2024.

Abstract

Tumor tissues are well known for their unique high hydrogen peroxide (HO) microenvironment. How to exploit this tumor microenvironment for tumor cell killing is a question. In this study, a Mn-doped metal-organic framework (Mn-ZIF) was constructed. It possesses good peroxidase (POD) activity, which can oxidize tumor-localized HO into hydroxyl radicals (·OH), that possesses the ability to directly kill tumor cells. More surprisingly, experiments the researchers not only observed the tumor-killing effect of Mn-ZIF, but also found it changes in macrophage phenotype in the tumor region. There was an increase in macrophage polarization towards the M1 subtype. This suggests that the tumor-killing effect of Mn-ZIF not only comes from its POD activity, but also regulates the immune microenvironment in the tumor region. In conclusion, the preparation of Mn-ZIF provides a new way for comprehensive tumor therapy.

摘要

肿瘤组织以其独特的高过氧化氢(HO)微环境而闻名。如何利用这种肿瘤微环境来杀死肿瘤细胞是一个问题。在本研究中,构建了一种锰掺杂的金属有机框架(Mn-ZIF)。它具有良好的过氧化物酶(POD)活性,可将肿瘤局部的HO氧化为羟基自由基(·OH),而羟基自由基具有直接杀死肿瘤细胞的能力。更令人惊讶的是,研究人员在实验中不仅观察到了Mn-ZIF的肿瘤杀伤作用,还发现它改变了肿瘤区域巨噬细胞的表型。巨噬细胞向M1亚型的极化有所增加。这表明Mn-ZIF的肿瘤杀伤作用不仅来自其POD活性,还能调节肿瘤区域的免疫微环境。总之,Mn-ZIF的制备为综合肿瘤治疗提供了一种新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8235/11347784/edc6109c961c/FPHAR_fphar-2024-1441818_wc_sch1.jpg

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