A Copper‐Manganese Based Nanocomposite Induces Cuproptosis and Potentiates Anti‐Tumor Immune Responses

Cancer is one of the most important challenges worldwide with an increasing incidence. However, most of patients with malignant cancer receiving traditional therapies have tumor recurrence and short-term 5-year survival. Herein, a novel Cu<sub>2</sub>O-MnO@PEG (CMP) nanomaterial is developed to treat tumors. CMP directly mediates cuproptosis in tumor cells. Meanwhile, CMP potentiates anti-tumor immune responses in the tumor microenvironment (TME) to induce tumor regression. CMP improves the tumor antigen processing and presentation of dendritic cells and tumor-associated macrophages, and further promotes CD8<sup>+</sup> T cell responses, especially for cytotoxic CD8<sup>+</sup> T cells and transitory exhausted CD8<sup>+</sup> T cells. Additionally, CMP downregulates the proportion of Treg cells and CTLA-4 expression on Treg cells. Notably, CMP induces systemic immune responses against distant tumors and long-term immune memory. Furthermore, CMP synergized with PD-L1 mAb promotes tumor inhibition and sustains the anti-tumor efficacy post PD-L1 mAb treatment. Collectively, this strategy has the clinically therapeutic potential for tumors by facilitating cuproptosis in tumor cells and anti-tumor immune responses.

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Publication Details

Journal
Small
Published
2025-02-16
DOI
https://doi.org/10.1002/smll.202412174
Citations
9
Primary Topic
Nanoparticle-Based Drug Delivery
Type
article
Field-Weighted Citation Impact
5.37

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article

A Copper‐Manganese Based Nanocomposite Induces Cuproptosis and Potentiates Anti‐Tumor Immune Responses

Zhongjun Wu, Xianxing Wang, Pijiang Sun, Weinan Zhang et al.
9 citations
Small
Nanoparticle-Based Drug Delivery
5.37
article

A Copper‐Manganese Based Nanocomposite Induces Cuproptosis and Potentiates Anti‐Tumor Immune Responses

Zhongjun Wu, Xianxing Wang, Pijiang Sun, Weinan Zhang, S. David Wu, Luoyingzi Xie, Haoyu Wang, Jie Gong, Lei Cai, Huaizhi Wang, Zhiqiang He
article en
9 citations

Abstract

Cancer is one of the most important challenges worldwide with an increasing incidence. However, most of patients with malignant cancer receiving traditional therapies have tumor recurrence and short-term 5-year survival. Herein, a novel Cu<sub>2</sub>O-MnO@PEG (CMP) nanomaterial is developed to treat tumors. CMP directly mediates cuproptosis in tumor cells. Meanwhile, CMP potentiates anti-tumor immune responses in the tumor microenvironment (TME) to induce tumor regression. CMP improves the tumor antigen processing and presentation of dendritic cells and tumor-associated macrophages, and further promotes CD8<sup>+</sup> T cell responses, especially for cytotoxic CD8<sup>+</sup> T cells and transitory exhausted CD8<sup>+</sup> T cells. Additionally, CMP downregulates the proportion of Treg cells and CTLA-4 expression on Treg cells. Notably, CMP induces systemic immune responses against distant tumors and long-term immune memory. Furthermore, CMP synergized with PD-L1 mAb promotes tumor inhibition and sustains the anti-tumor efficacy post PD-L1 mAb treatment. Collectively, this strategy has the clinically therapeutic potential for tumors by facilitating cuproptosis in tumor cells and anti-tumor immune responses.

SmallVol. 21(12)
Chongqing University (CN), Dalian Medical University (CN), Leshan Normal University (CN), Second Affiliated Hospital of Chongqing Medical University (CN), The Affiliated Yongchuan Hospital of Chongqing Medical University (CN), Southwest Hospital (CN), Chongqing Medical University (CN)
Chongqing Municipal Health Commission, National Natural Science Foundation of China, Chongqing Municipal Human Resources and Social Security Bureau
Openalex Percentile: Top 4%
Nanoparticle-Based Drug Delivery
5.37
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