# Copper-enriched zinc peroxides induced cuproptosis through concurrent metabolic and oxidative dysregulation for boosting immunotherapy in colorectal cancer

**Authors:** Shaopeng Zhang, Shaokang Yang, Mingqi Li, Hao Zhang, Yue Cao, Shiqi Bai, Wei Li, Bin Wang, Donghao Qu, Ziqian Wang, Wanying Li, Yanxu Sun, Daguang Wang, Yinghui Wang, Hongjie Zhang

PMC · DOI: 10.1016/j.mtbio.2026.102830 · Materials Today Bio · 2026-01-19

## TL;DR

A new nanoplatform induces cuproptosis in colorectal cancer, enhancing immune response and improving immunotherapy outcomes.

## Contribution

A TME-responsive biodegradable nanoplatform (ZCH) is developed to induce cuproptosis and boost immunotherapy.

## Key findings

- ZCH enables controlled Cu2+ release in tumors, inducing cuproptosis with reduced normal tissue toxicity.
- ZCH disrupts redox balance and glycolysis, triggering immunogenic cell death in colorectal cancer.
- The synergistic effects of copper accumulation and metabolic inhibition enhance antitumor immunity.

## Abstract

Despite the immunotherapy has achieved the progress for advanced colorectal cancer, the unsatisfactory treatment effect remains a challenge due to the deficient immune response. In this work, we constructed a tumor microenvironments (TME)-responsive biodegradable cuproptosis inducer (ZnO2-Cu@HA, ZCH) through cation-exchange method for amplifying the immune response. Compared to free copper ions, ZCH cloud achieve the controllable release of Cu2+ in tumor site, trggering efficient cuproptosis but reducing the side effect of normal tissues. Furthermore, the released Zn2+ could also inhibit intracellular glycolysis and ATP generation, then block the ATP7B to reduce the efflux of copper ions. Meanwhile, ZCH broke intracellular redox homeostasis via the release of exogenous H2O2, Cu+-mediated Fenton-like reaction and Zn2+-induced endogenous mitoROS, amplifying the cuproptosis to inducing immunogenic cell death (ICD) triggered for highly efficient immunotherapy of colorectal cancer. These findings demonstrated that it is a promising strategy of inducing efficient cuproptosis by the synergistic effect of accumulation of copper ions, inhibiting glycolysis and down-regulation GSH for efficient immunotherapy of colorectal cancer.

A novel TME-responsive biodegradable nanoplatform (ZnO2-Cu@HA, ZCH) was constructed by doping copper ions through cation-exchange method before functionalized with hyaluronic acid (HA) for inducing the efficient antitumor immune response mediated by cuproptosis. The nanoplatform inducing cuproptosis by accumulation of copper ions, inhibiting glycolysis and down-regulation GSH has a promising potential to induce immune response for boosting colorectal cancer immunotherapy.Image 1

## Linked entities

- **Chemicals:** Cu2+ (PubChem CID 27099), Zn2+ (PubChem CID 32051), H2O2 (PubChem CID 784), GSH (PubChem CID 124886)
- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Genes:** ATP7B (ATPase copper transporting beta) [NCBI Gene 540] {aka PWD, WC1, WD, WND}
- **Diseases:** tumor (MESH:D009369), colorectal cancer (MESH:D015179)
- **Chemicals:** GSH (MESH:D005978), Cu@HA (-), ATP (MESH:D000255), Copper (MESH:D003300), H2O2 (MESH:D006861)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12858360/full.md

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12858360/full.md

## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC12858360/full.md

---
Source: https://tomesphere.com/paper/PMC12858360