Metabolic Inhibitor Loaded Metal–Phenolic Nanocapsules Enable Synergistic Cancer Therapy through Cuproptosis and Immunometabolic Reprogramming

Abnormal glycolysis and glutamine metabolism not only sustain tumor growth but also reprogram the tumor microenvironment (TME). However, due to compensatory mechanisms and low tumor immunogenicity, targeting a single metabolic pathway is often insufficient for effective cancer therapy. We here developed dual-starvation therapeutic metal-phenolic nanocapsules (CG@Cap) by encapsulating a glutamine metabolism inhibitor with a zeolitic imidazolate framework-8 and adsorbing glucose oxidase on the surface, followed by coordination-driven assembly with tannic acid and copper ions. After preferential accumulation at tumor sites and internalization by tumor cells, the nanocapsules release their cargo, simultaneously suppressing glycolysis and glutamine metabolism. This dual inhibition disrupts tumor energy supply and remodels the immunosuppressive TME. Furthermore, the resulting redox imbalance enhances copper-induced cuproptosis, eliciting a strong antitumor immune response. In tumor-bearing mice, CG@Cap demonstrated potent therapeutic efficacy, highlighting the promise of integrating immunometabolic reprogramming with cuproptosis induction for cancer therapy.

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Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2025-09-04
DOI
https://doi.org/10.1021/acsami.5c10711
Citations
1
Primary Topic
Autophagy in Disease and Therapy
Type
article
Field-Weighted Citation Impact
1.35

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article

Metabolic Inhibitor Loaded Metal–Phenolic Nanocapsules Enable Synergistic Cancer Therapy through Cuproptosis and Immunometabolic Reprogramming

Houyang Hu, Songyan Li, Fenglei Xu, Guiqiang Zhang et al.
1 citations
ACS Applied Materials & Interfaces
Autophagy in Disease and Therapy
1.35
article

Metabolic Inhibitor Loaded Metal–Phenolic Nanocapsules Enable Synergistic Cancer Therapy through Cuproptosis and Immunometabolic Reprogramming

Houyang Hu, Songyan Li, Fenglei Xu, Guiqiang Zhang, Xiuying Duan, Zilin Ma, Bin Li, Xuechun Wang, Y. X. Song, Wen Chao Zhao, Jianwei Jiao
article en
1 citations

Abstract

Abnormal glycolysis and glutamine metabolism not only sustain tumor growth but also reprogram the tumor microenvironment (TME). However, due to compensatory mechanisms and low tumor immunogenicity, targeting a single metabolic pathway is often insufficient for effective cancer therapy. We here developed dual-starvation therapeutic metal-phenolic nanocapsules (CG@Cap) by encapsulating a glutamine metabolism inhibitor with a zeolitic imidazolate framework-8 and adsorbing glucose oxidase on the surface, followed by coordination-driven assembly with tannic acid and copper ions. After preferential accumulation at tumor sites and internalization by tumor cells, the nanocapsules release their cargo, simultaneously suppressing glycolysis and glutamine metabolism. This dual inhibition disrupts tumor energy supply and remodels the immunosuppressive TME. Furthermore, the resulting redox imbalance enhances copper-induced cuproptosis, eliciting a strong antitumor immune response. In tumor-bearing mice, CG@Cap demonstrated potent therapeutic efficacy, highlighting the promise of integrating immunometabolic reprogramming with cuproptosis induction for cancer therapy.

ACS Applied Materials & InterfacesVol. 17(37)
Academy of Medical Sciences (GB), University of Medical Sciences and Technology (SD), Chinese Academy of Sciences (CN), Shandong Provincial Hospital (CN), Shandong First Medical University (CN), Institute of Zoology (CN), State Key Laboratory of Stem Cell and Reproductive Biology
National Natural Science Foundation of China, Natural Science Foundation of Shandong Province, Shandong First Medical University
Openalex Percentile: Top 16%
Autophagy in Disease and Therapy
1.35
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