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铜死亡在癌症中的作用:生物学意义和治疗机会。

Cuproptosis in cancer: biological implications and therapeutic opportunities.

机构信息

Department of Pharmacy, Chengdu Fifth People's Hospital, Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, People's Republic of China.

Division of Abdominal Cancer, Department of Medical Oncology, Cancer Center and Laboratory of Molecular Targeted Therapy in Oncology, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, People's Republic of China.

出版信息

Cell Mol Biol Lett. 2024 Jun 25;29(1):91. doi: 10.1186/s11658-024-00608-3.


DOI:10.1186/s11658-024-00608-3
PMID:38918694
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11201306/
Abstract

Cuproptosis, a newly identified copper (Cu)-dependent form of cell death, stands out due to its distinct mechanism that sets it apart from other known cell death pathways. The molecular underpinnings of cuproptosis involve the binding of Cu to lipoylated enzymes in the tricarboxylic acid cycle. This interaction triggers enzyme aggregation and proteotoxic stress, culminating in cell death. The specific mechanism of cuproptosis has yet to be fully elucidated. This newly recognized form of cell death has sparked numerous investigations into its role in tumorigenesis and cancer therapy. In this review, we summarized the current knowledge on Cu metabolism and its link to cancer. Furthermore, we delineated the molecular mechanisms of cuproptosis and summarized the roles of cuproptosis-related genes in cancer. Finally, we offered a comprehensive discussion of the most recent advancements in Cu ionophores and nanoparticle delivery systems that utilize cuproptosis as a cutting-edge strategy for cancer treatment.

摘要

铜死亡,一种新发现的依赖铜的细胞死亡形式,因其独特的机制而引人注目,与其他已知的细胞死亡途径不同。铜死亡的分子基础涉及到三羧酸循环中脂酰化酶与铜的结合。这种相互作用引发酶聚集和蛋白毒性应激,最终导致细胞死亡。铜死亡的具体机制尚未完全阐明。这种新发现的细胞死亡形式引发了大量关于其在肿瘤发生和癌症治疗中的作用的研究。在这篇综述中,我们总结了目前关于铜代谢及其与癌症的关系的知识。此外,我们描述了铜死亡的分子机制,并总结了铜死亡相关基因在癌症中的作用。最后,我们全面讨论了最近在铜离子载体和纳米颗粒传递系统方面的进展,这些系统将铜死亡作为一种治疗癌症的前沿策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4c7/11201306/adf1a8c29617/11658_2024_608_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4c7/11201306/6a8ea442688e/11658_2024_608_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4c7/11201306/99a0c4caabb8/11658_2024_608_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4c7/11201306/adf1a8c29617/11658_2024_608_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4c7/11201306/6a8ea442688e/11658_2024_608_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4c7/11201306/99a0c4caabb8/11658_2024_608_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4c7/11201306/adf1a8c29617/11658_2024_608_Fig3_HTML.jpg

相似文献

[1]
Cuproptosis in cancer: biological implications and therapeutic opportunities.

Cell Mol Biol Lett. 2024-6-25

[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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引用本文的文献

[1]
Metabolic cell death in cancer: mechanisms and therapeutic potential.

Apoptosis. 2025-9-9

[2]
Cuproptosis-driven nanostrategies: Synergistic nanoplatforms for tumor microenvironment reprogramming and enhanced anticancer efficacy.

Mater Today Bio. 2025-5-21

[3]
Cuproptosis-related genes and agents: implications in tumor drug resistance and future perspectives.

Front Pharmacol. 2025-5-8

[4]
Novel cuproptosis-related lncRNAs risk model to predicting prognosis and guiding immunotherapy for OSCC patients.

Discov Oncol. 2025-5-11

[5]
Targeting pyroptosis for cancer immunotherapy: mechanistic insights and clinical perspectives.

Mol Cancer. 2025-5-3

[6]
PER2 interaction with HSP70 promotes cuproptosis in oral squamous carcinoma cells by decreasing AKT stability.

Cell Death Dis. 2025-3-20

[7]
Targeting the initiator to activate both ferroptosis and cuproptosis for breast cancer treatment: progress and possibility for clinical application.

Front Pharmacol. 2025-1-10

[8]
Comprehensive analysis of cuproptosis-related genes involved in prognosis and tumor microenvironment infiltration of colorectal cancer.

Transl Cancer Res. 2024-9-30

[9]
lncRNAs as prognostic markers and therapeutic targets in cuproptosis-mediated cancer.

Clin Exp Med. 2024-9-26

[10]
Targeting cuproptosis for cancer therapy: mechanistic insights and clinical perspectives.

J Hematol Oncol. 2024-8-16

本文引用的文献

[1]
Inhalable metal-organic framework-mediated cuproptosis combined with PD-L1 checkpoint blockade for lung metastasis synergistic immunotherapy.

Acta Pharm Sin B. 2024-5

[2]
Hyperbaric Oxygen Boosts Antitumor Efficacy of Copper-Diethyldithiocarbamate Nanoparticles against Pancreatic Ductal Adenocarcinoma by Regulating Cancer Stem Cell Metabolism.

Research (Wash D C). 2024-3-11

[3]
Comprehensive molecular analyses of cuproptosis-related genes with regard to prognosis, immune landscape, and response to immune checkpoint blockers in lung adenocarcinoma.

J Cancer Res Clin Oncol. 2024-5-9

[4]
Revealing the potential of solute carrier family 31 (copper transporters), member 1: Insights into its role in bladder cancer progression and therapeutic implications.

Int J Immunopathol Pharmacol. 2024

[5]
Identification of 10 differentially expressed and cuproptosis-related genes in immune infiltration and prognosis of thyroid carcinoma.

Cell Mol Biol (Noisy-le-grand). 2024-3-31

[6]
Cuproptosis-Related Gene FDX1 Suppresses the Growth and Progression of Colorectal Cancer by Retarding EMT Progress.

Biochem Genet. 2025-2

[7]
Identification and validation of a novel cuproptosis signature for stratifying different prognostic, immune, metabolic, and therapeutic landscapes in pancreatic adenocarcinoma.

Eur Rev Med Pharmacol Sci. 2024-3

[8]
Comprehensive analysis of the effects of the cuprotosis-associated gene on patient prognosis and tumor microenvironment in human cancer.

Transl Cancer Res. 2024-2-29

[9]
Multifunctional nanomaterials cell cuproptosis and oxidative stress for treating osteosarcoma and OS-induced bone destruction.

Mater Today Bio. 2024-2-15

[10]
Single-Site Nanozymes with a Highly Conjugated Coordination Structure for Antitumor Immunotherapy via Cuproptosis and Cascade-Enhanced T Lymphocyte Activity.

J Am Chem Soc. 2024-2-14

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