糖酵解干预诱导级联癌症治疗的自动代谢调节剂

IF 15.5
BMEMat Pub Date : 2024-10-22 DOI:10.1002/bmm2.12125
Jiao Zheng, Jian Zhang, Tian Zhang, Yongcun Yan, Sai Bi
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引用次数: 0

摘要

有效干预糖酵解代谢是抑制肿瘤恶性侵袭的有效途径。然而,其固有的缺氧环境和单一的调节模式影响了其治疗效果。本文通过将葡萄糖氧化酶(GOx)和dna模板银纳米团簇(DNA-AgNCs)加载到ph响应型沸石咪唑酸框架-8 (ZIF-8)纳米载体中,开发了一种设计自动代谢调节剂(auto-MMOD)的简便方法,该载体可以在GOx调节的糖酵解代谢过程中激活级联金属离子杀伤效应。当酸性溶酶体微环境诱导ZIF-8分解时,释放的GOx能有效消耗葡萄糖,生成H2O2,从而抑制三磷酸腺苷合成,加速肿瘤饥饿。此外,H2O2作用下释放的Ag+可以扰乱生物能量代谢,抑制肿瘤增殖,进一步增强了缺氧微环境下的抑瘤作用。本研究将离子治疗与糖酵解干预相结合,在体外和体内实现了有效的肿瘤抑制,为纳米治疗奠定了良好的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Automatic metabolism modulator for glycolytic intervention-induced cascade cancer therapy

Automatic metabolism modulator for glycolytic intervention-induced cascade cancer therapy

Effective intervention in glycolytic metabolism is a promising way to inhibit tumor malignant invasion. However, the inherent hypoxia environment and unitary regulating model subsequently compromise its therapeutic efficacy. Herein, a facile way to design an automatic metabolism modulator (auto-MMOD) is developed by loading glucose oxidase (GOx) and DNA-templated silver nanoclusters (DNA-AgNCs) into a pH-responsive zeolitic imidazolate frameworks-8 (ZIF-8) nanocarrier, which can activate a cascaded metal ion-killing effect during GOx-regulated glycolysis metabolism. When the acidic lysosome microenvironment induces ZIF-8 decomposition, the released GOx can effectively consume glucose and generate H2O2, thus inhibiting Adenosine Triphosphate synthesis and accelerating tumor starvation. Moreover, the released Ag+ in response to H2O2 can disturb bioenergy metabolism to inhibit tumor proliferation, which further enhances the tumor-killing effect in hypoxic microenvironments. This study achieves effective tumor suppression in vitro and in vivo by integrating ion therapy into glycolysis intervention, which establish a promising strategy for nano-theranostics.

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