# Clinically friendly smart hydrogel boosts cuproptosis and PD-L1 upregulation to enhance anti-tumor immunotherapy

**Authors:** Baiyang Fu, Guangyan Li, Yuan Yao, Mingfu Zhang, Yesheng Zhong, Xi Wang, Yichi Chen, Wenlong Liang, Yao Wang, Haiyun Lin, Yutong Zhang, Qiguang Du, Zhongkai Xu, He Cui, Liping Shi, Xi Chen, Jianguo Zhang

PMC · DOI: 10.1016/j.mtbio.2025.102268 · 2025-09-09

## TL;DR

A smart hydrogel combining cuproptosis and immunotherapy effectively treats triple-negative breast cancer by boosting anti-tumor immune responses.

## Contribution

A novel temperature/pH-responsive hydrogel integrates cuproptosis, starvation therapy, chemodynamic therapy, and immunotherapy for TNBC treatment.

## Key findings

- ES-Cu&GOx@FFC synergistically triggers cuproptosis and chemodynamic therapy in TNBC.
- The hydrogel upregulates PD-L1 and improves tumor regression when combined with αPD-L1 immunotherapy.
- The treatment achieves over 90% tumor volume regression in combined therapy experiments.

## Abstract

Triple-negative breast cancer (TNBC) faces the challenge of limited treatment efficacy due to its highly invasive ability and its immunosuppressive microenvironment. This study found that cuproptosis, as an emerging therapeutic strategy, has unique therapeutic potential in TNBC. Nevertheless, the delivery difficulties of cuproptosis-inducing agents and the limited efficacy of single drugs restrict the clinical application of cuproptosis therapy. Herein, a temperature/pH dual-responsive composite hydrogel was developed to load Elesclomol-Cu (ES-Cu) and glucose oxidase (GOx) (ES-Cu&GOx@FFC). ES and Cu2+ can synergistically trigger cuproptosis in TNBC, and GOx can not only inhibit tumor metabolism by mediating glucose deprivation but also initiate the Fenton reaction by continuously generating H2O2 and synergizing with copper ions, driving a potent chemodynamic therapy (CDT). Furthermore, ES-Cu&GOx@FFC could significantly improve the immunosuppressive landscape and upregulate programmed death-ligand 1 (PD-L1) expression in TNBC. Combined therapy experiments showed that the combination treatment of ES-Cu&GOx@FFC and αPD-L1 achieved more than 90 % tumor volume regression. In summary, this study provides new insights into the therapeutic role of cuproptosis in TNBC, and integrates cuproptosis, starvation therapy, CDT, and immunotherapy through smart responsive hydrogels, providing an innovative solution for the treatment of TNBC.

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## Linked entities

- **Proteins:** CD274 (CD274 molecule)
- **Chemicals:** Elesclomol-Cu (PubChem CID 86289903), glucose oxidase (PubChem CID 206), Cu2+ (PubChem CID 27099), H2O2 (PubChem CID 784)
- **Diseases:** triple-negative breast cancer (MONDO:0005494)

## Full-text entities

- **Genes:** CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, HAO1 (hydroxyacid oxidase 1) [NCBI Gene 54363] {aka GO, GOX, GOX1, HAOX1}
- **Diseases:** tumor (MESH:D009369), TNBC (MESH:D064726)
- **Chemicals:** glucose (MESH:D005947), Cu2+ (-), copper (MESH:D003300), H2O2 (MESH:D006861)

## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12859559/full.md

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Source: https://tomesphere.com/paper/PMC12859559