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铜死亡与铜死亡相关基因:乳腺癌中新兴的潜在治疗靶点

Cuproptosis and cuproptosis-related genes: Emerging potential therapeutic targets in breast cancer.

作者信息

Liu Xiangdong, Luo Bo, Wu Xinhong, Tang Zijian

机构信息

Department of Radiotherapy Center, Hubei Cancer Hospital, The Seventh Clinical School Affiliated of Tongji Medical College, Huazhong University of Science and Technology, Hubei Provincial Clinical Research Center for Breast Cancer, Wuhan Clinical Research Center for Breast Cancer, Wuhan 430079, China.

Department of Radiotherapy Center, Hubei Cancer Hospital, The Seventh Clinical School Affiliated of Tongji Medical College, Huazhong University of Science and Technology, Hubei Provincial Clinical Research Center for Breast Cancer, Wuhan Clinical Research Center for Breast Cancer, Wuhan 430079, China.

出版信息

Biochim Biophys Acta Rev Cancer. 2023 Nov;1878(6):189013. doi: 10.1016/j.bbcan.2023.189013. Epub 2023 Oct 31.


DOI:10.1016/j.bbcan.2023.189013
PMID:37918452
Abstract

Breast cancer is one of the most common malignant tumors in women worldwide, and thus, it is important to enhance its treatment efficacy [1]. Copper has emerged as a critical trace element that affects various intracellular signaling pathways, gene expression, and biological metabolic processes [2], thereby playing a crucial role in the pathogenesis of breast cancer. Recent studies have identified cuproptosis, a newly discovered type of cell death, as an emerging therapeutic target for breast cancer treatment, thereby offering new hope for breast cancer patients. Tsvetkov's research has elucidated the mechanism of cuproptosis and uncovered the critical genes involved in its regulation [3]. Manipulating the expression of these genes could potentially serve as a promising therapeutic strategy for breast cancer treatment. Additionally, using copper ionophores and copper complexes combined with nanomaterials to induce cuproptosis may provide a potential approach to eliminating drug-resistant breast cancer cells, thus improving the therapeutic efficacy of chemotherapy, radiotherapy, and immunotherapy and eventually eradicating breast tumors. This review aims to highlight the practical significance of cuproptosis-related genes and the induction of cuproptosis in the clinical diagnosis and treatment of breast cancer. We examine the potential of cuproptosis as a novel therapeutic target for breast cancer, and we explore the present challenges and limitations of this approach. Our objective is to provide innovative ideas and references for the development of breast cancer treatment strategies based on cuproptosis.

摘要

乳腺癌是全球女性中最常见的恶性肿瘤之一,因此,提高其治疗效果至关重要[1]。铜已成为一种关键的微量元素,影响各种细胞内信号通路、基因表达和生物代谢过程[2],从而在乳腺癌的发病机制中发挥关键作用。最近的研究已确定铜死亡,一种新发现的细胞死亡类型,是乳腺癌治疗的新兴治疗靶点,从而为乳腺癌患者带来了新希望。茨韦特科夫的研究阐明了铜死亡的机制,并发现了参与其调控的关键基因[3]。操纵这些基因的表达可能成为乳腺癌治疗的一种有前景的治疗策略。此外,使用铜离子载体和铜配合物与纳米材料相结合来诱导铜死亡,可能提供一种消除耐药乳腺癌细胞的潜在方法,从而提高化疗、放疗和免疫治疗的疗效,并最终根除乳腺肿瘤。本综述旨在强调铜死亡相关基因以及诱导铜死亡在乳腺癌临床诊断和治疗中的实际意义。我们研究了铜死亡作为乳腺癌新治疗靶点的潜力,并探讨了这种方法目前面临的挑战和局限性。我们的目标是为基于铜死亡的乳腺癌治疗策略的发展提供创新思路和参考。

相似文献

[1]
Cuproptosis and cuproptosis-related genes: Emerging potential therapeutic targets in breast cancer.

Biochim Biophys Acta Rev Cancer. 2023-11

[2]
Cuproptosis: A novel therapeutic target for overcoming cancer drug resistance.

Drug Resist Updat. 2024-1

[3]
Comprehensive analysis of cuproptosis-related genes and tumor microenvironment infiltration characterization in breast cancer.

Front Immunol. 2022

[4]
Biomimetic copper-doped polypyrrole nanoparticles induce glutamine metabolism inhibition to enhance breast cancer cuproptosis and immunotherapy.

J Control Release. 2024-7

[5]
Prognostic and immune microenvironment analysis of cuproptosis-related LncRNAs in breast cancer.

Funct Integr Genomics. 2023-1-14

[6]
Repositioning fluphenazine as a cuproptosis-dependent anti-breast cancer drug candidate based on TCGA database.

Biomed Pharmacother. 2024-9

[7]
Crosstalk between ferroptosis and cuproptosis: From mechanism to potential clinical application.

Biomed Pharmacother. 2024-2

[8]
Cuproptosis, the novel type of oxidation-induced cell death in thoracic cancers: can it enhance the success of immunotherapy?

Cell Commun Signal. 2024-7-27

[9]
Comprehensive Analysis of Cuproptosis Genes and Identification of Cuproptosis Subtypes in Breast Cancer.

Comb Chem High Throughput Screen. 2023

[10]
Identification of cuproptosis -related subtypes, the development of a prognosis model, and characterization of tumor microenvironment infiltration in prostate cancer.

Front Immunol. 2022

引用本文的文献

[1]
Engineered RAP-anchored copper-escorting liposomes for FDX1-targeted cuproptosis in glioblastoma therapy‌.

Theranostics. 2025-7-2

[2]
Hypoxia, cuproptosis, and osteoarthritis: Unraveling the molecular crosstalk.

Redox Biol. 2025-7-8

[3]
PDHA1 Orchestrates Hepatocellular Carcinoma Progression Through LINC00607-Mediated Regulation of Cuproptosis and Immune Evasion.

Dig Dis Sci. 2025-6-18

[4]
Modulation of copper homeostasis and cuproptosis by PDHA1 in acute myeloid leukemia.

Discov Oncol. 2025-6-10

[5]
Cuproptosis-related genes and agents: implications in tumor drug resistance and future perspectives.

Front Pharmacol. 2025-5-8

[6]
Targeting the Enhanced Sensitivity of Radiotherapy in Cancer: Mechanisms, Applications, and Challenges.

MedComm (2020). 2025-5-15

[7]
Novel cuproptosis-related lncRNAs risk model to predicting prognosis and guiding immunotherapy for OSCC patients.

Discov Oncol. 2025-5-11

[8]
Common Regulatory Mechanisms Mediated by Cuproptosis Genes in Inflammatory Bowel Disease and Major Depressive Disorder.

Genes (Basel). 2025-3-14

[9]
Integrated bulk and single-cell transcriptomic analysis unveiled a novel cuproptosis-related lipid metabolism gene molecular pattern and a risk index for predicting prognosis and antitumor drug sensitivity in breast cancer.

Discov Oncol. 2025-3-14

[10]
Big data analysis and machine learning of the role of cuproptosis-related long non-coding RNAs (CuLncs) in the prognosis and immune landscape of ovarian cancer.

Front Immunol. 2025-2-25

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