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铜死亡:揭示癌症生物学和治疗学的新前沿。

Cuproptosis: unveiling a new frontier in cancer biology and therapeutics.

机构信息

Department of Emergency, the Affiliated Hospital of Qingdao University, No. 16 Jiangsu Road, Qingdao, 266005, Shandong, China.

Department of Neurosurgery, 3201 Hospital of Xi'an Jiaotong University Health Science Center, Hanzhong, 723000, Shaanxi, China.

出版信息

Cell Commun Signal. 2024 May 1;22(1):249. doi: 10.1186/s12964-024-01625-7.


DOI:10.1186/s12964-024-01625-7
PMID:38693584
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11064406/
Abstract

Copper plays vital roles in numerous cellular processes and its imbalance can lead to oxidative stress and dysfunction. Recent research has unveiled a unique form of copper-induced cell death, termed cuproptosis, which differs from known cell death mechanisms. This process involves the interaction of copper with lipoylated tricarboxylic acid cycle enzymes, causing protein aggregation and cell death. Recently, a growing number of studies have explored the link between cuproptosis and cancer development. This review comprehensively examines the systemic and cellular metabolism of copper, including tumor-related signaling pathways influenced by copper. It delves into the discovery and mechanisms of cuproptosis and its connection to various cancers. Additionally, the review suggests potential cancer treatments using copper ionophores that induce cuproptosis, in combination with small molecule drugs, for precision therapy in specific cancer types.

摘要

铜在许多细胞过程中发挥着至关重要的作用,其失衡可导致氧化应激和功能障碍。最近的研究揭示了一种独特的铜诱导细胞死亡形式,称为铜死亡,它不同于已知的细胞死亡机制。这个过程涉及铜与脂酰化三羧酸循环酶的相互作用,导致蛋白质聚集和细胞死亡。最近,越来越多的研究探讨了铜死亡与癌症发展之间的联系。这篇综述全面考察了铜的系统和细胞代谢,包括受铜影响的肿瘤相关信号通路。它深入探讨了铜死亡的发现和机制,以及它与各种癌症的联系。此外,该综述还提出了使用铜离子载体诱导铜死亡的潜在癌症治疗方法,结合小分子药物,用于特定癌症类型的精准治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01c/11064406/47963f1fd286/12964_2024_1625_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01c/11064406/351c77f5f6a4/12964_2024_1625_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01c/11064406/1cdc3f3303a4/12964_2024_1625_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01c/11064406/5bc5a13d95e7/12964_2024_1625_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01c/11064406/96f95546e06d/12964_2024_1625_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01c/11064406/cac3f9077434/12964_2024_1625_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01c/11064406/69a2fc2f88e5/12964_2024_1625_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01c/11064406/5456bdd50dff/12964_2024_1625_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01c/11064406/e432001419ab/12964_2024_1625_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01c/11064406/47963f1fd286/12964_2024_1625_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01c/11064406/351c77f5f6a4/12964_2024_1625_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01c/11064406/1cdc3f3303a4/12964_2024_1625_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01c/11064406/5bc5a13d95e7/12964_2024_1625_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01c/11064406/96f95546e06d/12964_2024_1625_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01c/11064406/cac3f9077434/12964_2024_1625_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01c/11064406/69a2fc2f88e5/12964_2024_1625_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01c/11064406/5456bdd50dff/12964_2024_1625_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01c/11064406/e432001419ab/12964_2024_1625_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01c/11064406/47963f1fd286/12964_2024_1625_Fig9_HTML.jpg

相似文献

[1]
Cuproptosis: unveiling a new frontier in cancer biology and therapeutics.

Cell Commun Signal. 2024-5-1

[2]
Cuproptosis: a novel therapeutic mechanism in lung cancer.

Cancer Cell Int. 2025-6-24

[3]
Cuproptosis: Mechanisms, biological significance, and advances in disease treatment-A systematic review.

CNS Neurosci Ther. 2024-9

[4]
Cuproptosis: mechanisms and nanotherapeutic strategies in cancer and beyond.

Chem Soc Rev. 2025-6-30

[5]
Cuproptosis as the new kryptonite of cancer: a copper-dependent novel cell death mechanism with promising implications for the treatment of hepatocellular carcinoma.

J Cancer Res Clin Oncol. 2023-12

[6]
Dysregulated Wnt/β-catenin signaling confers resistance to cuproptosis in cancer cells.

Cell Death Differ. 2024-11

[7]
Cuproptosis: A Review on Mechanisms, Role in Solid and Hematological Tumors, and Association with Viral Infections.

Mediterr J Hematol Infect Dis. 2025-7-1

[8]
A tumor microenvironment-responsive nanocomposite for enhanced copper retention and hypoxia reversal to promote cuproptosis in tumor treatment.

Acta Biomater. 2025-7-4

[9]
Cuproptosis involvement in neonatal ischemic-hypoxic encephalopathy through the COMMD1/ATP7A signaling axis.

Biochem Pharmacol. 2025-9

[10]
LncRNA AP000842.3 Triggers the Malignant Progression of Prostate Cancer by Regulating Cuproptosis Related Gene NFAT5.

Technol Cancer Res Treat. 2024

引用本文的文献

[1]
Programmed Cell Death in Cancer.

MedComm (2020). 2025-8-31

[2]
Protein lipoylation in cancer: metabolic reprogramming and therapeutic potential.

Cell Death Discov. 2025-9-2

[3]
Mechanism of action of cuproptosis and prospects for anti-tumor therapy.

World J Clin Cases. 2025-8-26

[4]
Targeting cuproptosis opens a new chapter of nanomedicine: a scientometric and graphical analysis.

Naunyn Schmiedebergs Arch Pharmacol. 2025-8-12

[5]
Dissecting the intratumoral microbiome landscape in lung cancer.

Front Immunol. 2025-7-24

[6]
Deciphering Cuproptosis in Sepsis: Mechanisms, Consequences, and Therapeutic Opportunities.

J Inflamm Res. 2025-7-25

[7]
Exploring the synergetic role of cuproptosis and ferroptosis and their implication in advancing cancer therapeutics.

Discov Oncol. 2025-7-8

[8]
The emerging role of cuproptosis in spinal cord injury.

Front Immunol. 2025-6-16

[9]
Recent advances in regulatory immune cells: exploring the world beyond Tregs.

Front Immunol. 2025-5-16

[10]
Cuproptosis-related genes and agents: implications in tumor drug resistance and future perspectives.

Front Pharmacol. 2025-5-8

本文引用的文献

[1]
A Narrative Review of Current and Emerging Trends in the Treatment of Alcohol Use Disorder.

Brain Sci. 2024-3-20

[2]
Targeting cuproplasia and cuproptosis in cancer.

Nat Rev Clin Oncol. 2024-5

[3]
Modulation of immune-responses by DSF/Cu enhances the anti-tumor effects of DTX for metastasis breast cancer.

J Cancer. 2024-1-21

[4]
FDA-approved disulfiram as a novel treatment for aggressive leukemia.

J Mol Med (Berl). 2024-4

[5]
Cuproptosis: Unraveling the Mechanisms of Copper-Induced Cell Death and Its Implication in Cancer Therapy.

Cancers (Basel). 2024-2-2

[6]
Ferredoxin 1 is essential for embryonic development and lipid homeostasis.

Elife. 2024-1-22

[7]
Progress and Challenges in Tumor Ferroptosis Treatment Strategies: A Comprehensive Review of Metal Complexes and Nanomedicine.

Small. 2024-6

[8]
Copper homeostasis and cuproptosis in atherosclerosis: metabolism, mechanisms and potential therapeutic strategies.

Cell Death Discov. 2024-1-13

[9]
Crosstalk between ferroptosis and cuproptosis: From mechanism to potential clinical application.

Biomed Pharmacother. 2024-2

[10]
Metabolomic analyses uncover an inhibitory effect of niclosamide on mitochondrial membrane potential in cholangiocarcinoma cells.

PeerJ. 2023

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