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癌症中铜及铜死亡的分子机制与治疗前景

The molecular mechanism and therapeutic landscape of copper and cuproptosis in cancer.

作者信息

Guo Ziyu, Chen Danyao, Yao Lei, Sun Yuming, Li Daishi, Le Jiayuan, Dian Yating, Zeng Furong, Chen Xiang, Deng Guangtong

机构信息

Department of Dermatology, Xiangya Hospital, Central South University, Changsha, China.

National Engineering Research Center of Personalized Diagnostic and Therapeutic Technology, Changsha, China.

出版信息

Signal Transduct Target Ther. 2025 May 9;10(1):149. doi: 10.1038/s41392-025-02192-0.


DOI:10.1038/s41392-025-02192-0
PMID:40341098
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12062509/
Abstract

Copper, an essential micronutrient, plays significant roles in numerous biological functions. Recent studies have identified imbalances in copper homeostasis across various cancers, along with the emergence of cuproptosis, a novel copper-dependent form of cell death that is crucial for tumor suppression and therapeutic resistance. As a result, manipulating copper levels has garnered increasing interest as an innovative approach to cancer therapy. In this review, we first delineate copper homeostasis at both cellular and systemic levels, clarifying copper's protumorigenic and antitumorigenic functions in cancer. We then outline the key milestones and molecular mechanisms of cuproptosis, including both mitochondria-dependent and independent pathways. Next, we explore the roles of cuproptosis in cancer biology, as well as the interactions mediated by cuproptosis between cancer cells and the immune system. We also summarize emerging therapeutic opportunities targeting copper and discuss the clinical associations of cuproptosis-related genes. Finally, we examine potential biomarkers for cuproptosis and put forward the existing challenges and future prospects for leveraging cuproptosis in cancer therapy. Overall, this review enhances our understanding of the molecular mechanisms and therapeutic landscape of copper and cuproptosis in cancer, highlighting the potential of copper- or cuproptosis-based therapies for cancer treatment.

摘要

铜作为一种必需的微量营养素,在众多生物学功能中发挥着重要作用。最近的研究发现,在各种癌症中铜稳态存在失衡,同时出现了铜死亡,这是一种新的铜依赖性细胞死亡形式,对肿瘤抑制和治疗抗性至关重要。因此,调节铜水平作为一种创新的癌症治疗方法越来越受到关注。在这篇综述中,我们首先在细胞和全身水平上描述铜稳态,阐明铜在癌症中的促肿瘤和抗肿瘤功能。然后,我们概述铜死亡的关键里程碑和分子机制,包括线粒体依赖性和非依赖性途径。接下来,我们探讨铜死亡在癌症生物学中的作用,以及铜死亡介导的癌细胞与免疫系统之间的相互作用。我们还总结了针对铜的新兴治疗机会,并讨论了铜死亡相关基因的临床关联。最后,我们研究铜死亡的潜在生物标志物,并提出在癌症治疗中利用铜死亡存在的挑战和未来前景。总的来说,这篇综述增进了我们对癌症中铜和铜死亡的分子机制及治疗前景的理解,突出了基于铜或铜死亡的疗法在癌症治疗中的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e7d/12062509/4d41a354e7d6/41392_2025_2192_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e7d/12062509/38aac76f74fd/41392_2025_2192_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e7d/12062509/689ffbed6b1e/41392_2025_2192_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e7d/12062509/340fbf35b1d7/41392_2025_2192_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e7d/12062509/aa594862282a/41392_2025_2192_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e7d/12062509/cd0b02138a02/41392_2025_2192_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e7d/12062509/36563bef8c0c/41392_2025_2192_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e7d/12062509/4d41a354e7d6/41392_2025_2192_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e7d/12062509/38aac76f74fd/41392_2025_2192_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e7d/12062509/689ffbed6b1e/41392_2025_2192_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e7d/12062509/340fbf35b1d7/41392_2025_2192_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e7d/12062509/aa594862282a/41392_2025_2192_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e7d/12062509/cd0b02138a02/41392_2025_2192_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e7d/12062509/36563bef8c0c/41392_2025_2192_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e7d/12062509/4d41a354e7d6/41392_2025_2192_Fig7_HTML.jpg

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引用本文的文献

[1]
Machine learning-based model identifies a novel cuproptosis-related mitochondrial gene signature with a key role in the prognosis and treatment of lung adenocarcinoma.

Oncol Lett. 2025-8-21

[2]
Targeting cuproptosis opens a new chapter of nanomedicine: a scientometric and graphical analysis.

Naunyn Schmiedebergs Arch Pharmacol. 2025-8-12

[3]
Engineered anti-cancer nanomedicine for synergistic cuproptosis-immunotherapy.

Mater Today Bio. 2025-7-29

[4]
Targeting cuproptosis in liver cancer: Molecular mechanisms and therapeutic implications.

Apoptosis. 2025-8-7

[5]
Cuproptosis: a novel therapeutic mechanism in lung cancer.

Cancer Cell Int. 2025-6-24

[6]
Phase-transition engineered semi-metallic CuPdN for photothermal-enhanced cuproptosis-induced cancer therapy.

Mater Today Bio. 2025-5-29

本文引用的文献

[1]
Polyvalent Aptamer Nanodrug Conjugates Enable Efficient Tumor Cuproptosis Therapy Through Copper Overload and Glutathione Depletion.

J Am Chem Soc. 2024-11-6

[2]
Tumor Metabolism Aiming CuS Nanoagents Mediate Photothermal-Derived Cuproptosis and Immune Activation.

ACS Nano. 2024-9-3

[3]
Impact of SARS-CoV-2 infection on immune cell cuproptosis in patients with lung adenocarcinoma via glutamine regulation.

Int Immunopharmacol. 2024-10-25

[4]
Zinc transporter 1 functions in copper uptake and cuproptosis.

Cell Metab. 2024-9-3

[5]
Mitochondria-Targeted Multifunctional Nanoparticles Combine Cuproptosis and Programmed Cell Death-1 Downregulation for Cancer Immunotherapy.

Adv Sci (Weinh). 2024-9

[6]
Expression and Functional Analysis of the Metallothionein and Metal-Responsive Transcription Factor 1 in under Zn Stress.

Int J Mol Sci. 2024-7-5

[7]
Dysregulated Wnt/β-catenin signaling confers resistance to cuproptosis in cancer cells.

Cell Death Differ. 2024-11

[8]
Multifaceted Carbonized Metal-Organic Frameworks Synergize with Immune Checkpoint Inhibitors for Precision and Augmented Cuproptosis Cancer Therapy.

ACS Nano. 2024-7-9

[9]
Copper(II)-Based Nano-Regulator Correlates Cuproptosis Burst and Sequential Immunogenic Cell Death for Synergistic Cancer Immunotherapy.

Biomater Res. 2024-6-27

[10]
Glutathione-Scavenging Celastrol-Cu Nanoparticles Induce Self-Amplified Cuproptosis for Augmented Cancer Immunotherapy.

Adv Mater. 2024-8

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