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《进入睡眠者:如何应对休眠乳腺癌细胞》

Enter sandman: how to tackle dormant breast cancer cells.

作者信息

Attieh Fouad, Al Khatib Reina, Boutros Marc, Mouawad Antoine, Kourie Hampig Raphaël

机构信息

Faculty of Medicine, Saint Joseph University of Beirut, Beirut, 11072180, Lebanon.

Department of Hematology-Oncology, Faculty of Medicine, Saint Joseph University of Beirut, Beirut, 11072180, Lebanon.

出版信息

Med Oncol. 2025 Jun 18;42(7):271. doi: 10.1007/s12032-025-02833-y.

DOI:10.1007/s12032-025-02833-y
PMID:40533663
Abstract

Cancer dormancy poses a major challenge in oncology, often leading to relapse and metastasis years after initial treatment. This phenomenon is driven by the ability of dormant cancer cells to evade immune detection and resist chemotherapy. Thus, these cells remain in a quiescent state until conditions favor their reactivation. A deeper understanding of the mechanisms governing dormancy-including cellular signaling pathways, the role of the tumor microenvironment, and immune system interactions-is essential for developing effective and practical therapeutic interventions. Recent research has highlighted three primary strategies for targeting dormant breast cancer cells: the killing strategy, the sleeping strategy, and the awakening strategy. This review explores the various techniques used to detect dormant breast cancer cells and evaluates experimental therapeutic approaches aimed at either eradicating or controlling them. By synthesizing the latest advancements in cancer dormancy research, this article provides valuable insights for oncologists while remaining accessible to a broader audience.

摘要

癌症休眠是肿瘤学面临的一项重大挑战,常常导致在初始治疗数年之后出现复发和转移。这种现象是由休眠癌细胞逃避免疫检测和抵抗化疗的能力所驱动的。因此,这些细胞保持静止状态,直到条件有利于它们重新激活。深入了解控制休眠的机制——包括细胞信号通路、肿瘤微环境的作用以及免疫系统相互作用——对于开发有效且实用的治疗干预措施至关重要。最近的研究突出了针对休眠乳腺癌细胞的三种主要策略:杀伤策略、休眠策略和唤醒策略。本综述探讨了用于检测休眠乳腺癌细胞的各种技术,并评估了旨在根除或控制这些细胞的实验性治疗方法。通过综合癌症休眠研究的最新进展,本文为肿瘤学家提供了有价值的见解,同时也便于更广泛的读者理解。

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本文引用的文献

1
The GLOBOCAN 2022 cancer estimates: Data sources, methods, and a snapshot of the cancer burden worldwide.《2022年全球癌症统计报告》:数据来源、方法及全球癌症负担概述
Int J Cancer. 2025 Apr 1;156(7):1336-1346. doi: 10.1002/ijc.35278. Epub 2024 Dec 17.
2
A protein expression atlas on tissue samples and cell lines from cancer patients provides insights into tumor heterogeneity and dependencies.癌症患者的组织样本和细胞系的蛋白质表达图谱提供了对肿瘤异质性和依赖性的深入了解。
Nat Cancer. 2024 Oct;5(10):1579-1595. doi: 10.1038/s43018-024-00817-x. Epub 2024 Sep 3.
3
Epigenetic control of the vicious cycle.
恶性循环的表观遗传调控。
J Bone Oncol. 2024 Jan 12;44:100524. doi: 10.1016/j.jbo.2024.100524. eCollection 2024 Feb.
4
Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia.SCN8A 变异导致发作性或慢性共济失调的临床和电生理特征。
EBioMedicine. 2023 Dec;98:104855. doi: 10.1016/j.ebiom.2023.104855. Epub 2023 Oct 28.
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Immune evasion by dormant disseminated cancer cells: A Fermi paradox?休眠性播散癌细胞的免疫逃逸:费米悖论?
Cancer Cell. 2024 Jan 8;42(1):13-15. doi: 10.1016/j.ccell.2023.12.017.
6
Immune evasion of dormant disseminated tumor cells is due to their scarcity and can be overcome by T cell immunotherapies.休眠播散肿瘤细胞的免疫逃逸是由于其数量稀少,而T细胞免疫疗法可以克服这一问题。
Cancer Cell. 2024 Jan 8;42(1):119-134.e12. doi: 10.1016/j.ccell.2023.12.011.
7
A PERK-Specific Inhibitor Blocks Metastatic Progression by Limiting Integrated Stress Response-Dependent Survival of Quiescent Cancer Cells.一种 PERK 特异性抑制剂通过限制静止癌细胞中应激反应相关存活来阻止转移进展。
Clin Cancer Res. 2023 Dec 15;29(24):5155-5172. doi: 10.1158/1078-0432.CCR-23-1427.
8
Taxane chemotherapy induces stromal injury that leads to breast cancer dormancy escape.紫杉烷类化疗诱导基质损伤,导致乳腺癌休眠逃逸。
PLoS Biol. 2023 Sep 12;21(9):e3002275. doi: 10.1371/journal.pbio.3002275. eCollection 2023 Sep.
9
A cell cycle centric view of tumour dormancy.以细胞周期为中心的肿瘤休眠观点。
Br J Cancer. 2023 Nov;129(10):1535-1545. doi: 10.1038/s41416-023-02401-z. Epub 2023 Aug 22.
10
Association between 21-gene-assay and detection of disseminated tumor cells in patients with early breast cancer: results from the IRMA trial.21 基因检测与早期乳腺癌患者循环肿瘤细胞检测的相关性:IRMA 试验结果。
Breast Cancer Res Treat. 2023 Nov;202(1):67-72. doi: 10.1007/s10549-023-07031-w. Epub 2023 Aug 9.