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前列腺癌中的铜死亡:铜死亡相关基因的分子机制、预后生物标志物及治疗前沿(综述)

Cuproptosis in prostate cancer: Molecular mechanisms, prognostic biomarkers and therapeutic frontiers of cuproptosis‑related genes (Review).

作者信息

Long Zhugang, Chang Yue, Zhu Kun, Chen Zhengyang, You Yaodong

机构信息

Department of Urology/Andrology, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan 610072, P.R. China.

School of Clinical Medicine, Chengdu University of TCM, Chengdu, Sichuan 610075, P.R. China.

出版信息

Int J Oncol. 2025 Sep;67(3). doi: 10.3892/ijo.2025.5783. Epub 2025 Aug 8.


DOI:10.3892/ijo.2025.5783
PMID:40776742
Abstract

Prostate cancer (PCa) is among the most prevalent malignancies in males globally and management remains complex. In recent years, cuproptosis, an emerging form of cell death, has offered novel insights for PCa treatment. Cuproptosis refers to a copper‑mediated cellular death mechanism that is intricately associated with mitochondrial metabolism, with cuproptosis‑related genes (CRGs) exerting a notable effect on both cuproptosis and PCa. CRGs and other cuproptosis‑associated indicators have demonstrated efficacy as prognostic predictors of PCa and these predictors may exhibit potential as novel therapeutic targets in the treatment of PCa. The mechanisms underlying cuproptosis in PCa remain to be fully elucidated; thus, further research is required to validate the expression patterns of CRGs and their associated indicators and examine the potential association with the characteristics, treatment responses and prognoses of patients with PCa. The present study aimed to investigate novel therapeutic strategies that may enhance the prognosis and quality of life of patients with PCa.

摘要

前列腺癌(PCa)是全球男性中最常见的恶性肿瘤之一,其治疗仍然复杂。近年来,一种新出现的细胞死亡形式——铜死亡,为PCa的治疗提供了新的见解。铜死亡是指一种与线粒体代谢密切相关的铜介导的细胞死亡机制,铜死亡相关基因(CRGs)对铜死亡和PCa均有显著影响。CRGs和其他与铜死亡相关的指标已证明可作为PCa的预后预测指标,并且这些预测指标可能具有作为PCa治疗新靶点的潜力。PCa中铜死亡的潜在机制仍有待充分阐明;因此,需要进一步研究来验证CRGs及其相关指标的表达模式,并研究其与PCa患者的特征、治疗反应和预后的潜在关联。本研究旨在探索可能改善PCa患者预后和生活质量的新治疗策略。

相似文献

[1]
Cuproptosis in prostate cancer: Molecular mechanisms, prognostic biomarkers and therapeutic frontiers of cuproptosis‑related genes (Review).

Int J Oncol. 2025-9

[2]
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[3]
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[4]
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[5]
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[6]
Prognostic and Immunological Significance of the Molecular Subtypes and Risk Signatures Based on Cuproptosis in Hepatocellular Carcinoma.

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[7]
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Cancer Biol Ther. 2025-12

[8]
LncRNA AP000842.3 Triggers the Malignant Progression of Prostate Cancer by Regulating Cuproptosis Related Gene NFAT5.

Technol Cancer Res Treat. 2024

[9]
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[10]
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本文引用的文献

[1]
Identification of mitochondrial carrier homolog 2 as an important therapeutic target of castration-resistant prostate cancer.

Cell Death Dis. 2025-2-5

[2]
Complanatoside A disrupts copper homeostasis and induces cuproptosis via directly targeting ATOX1 in prostate cancer.

Toxicol Appl Pharmacol. 2025-3

[3]
Integrative analysis of cuproptosis-related lncRNAs: Unveiling prognostic significance, immune microenvironment, and copper-induced mechanisms in prostate cancer.

Cancer Pathog Ther. 2024-3-29

[4]
Cuproptosis-related lncRNAs emerge as a novel signature for predicting prognosis in prostate carcinoma and functional experimental validation.

Front Immunol. 2024

[5]
Analysis and functional validations of multiple cell death patterns for prognosis in prostate cancer.

Int Immunopharmacol. 2024-12-25

[6]
Construction of a cuproptosis‑related lncRNA signature to predict biochemical recurrence of prostate cancer.

Oncol Lett. 2024-9-3

[7]
Un-methylation of NUDT21 represses docosahexaenoic acid biosynthesis contributing to enzalutamide resistance in prostate cancer.

Drug Resist Updat. 2024-11

[8]
A systematic review of mechanisms of PTEN gene down-regulation mediated by miRNA in prostate cancer.

Heliyon. 2024-7-20

[9]
Establishment of a prognostic risk model for prostate cancer based on Gleason grading and cuprotosis related genes.

J Cancer Res Clin Oncol. 2024-8-1

[10]
Dysregulated Wnt/β-catenin signaling confers resistance to cuproptosis in cancer cells.

Cell Death Differ. 2024-11

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