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细胞外囊泡中的整合素在肿瘤微环境和转移中发挥作用。

Integrins from extracellular vesicles as players in tumor microenvironment and metastasis.

作者信息

Ciobanasu Corina, Le Clainche Christophe

机构信息

Department of Exact and Natural Sciences, Institute of Interdisciplinary Research, Alexandru I. Cuza University, Boulevard Carol I, Nr. 11, Iasi, 700506, Romania.

Institute for Integrative Biology of the Cell (I2BC), Université Paris-Saclay, CEA, CNRS, Gif-Sur-Yvette, 91198, France.

出版信息

Cancer Metastasis Rev. 2025 Sep 9;44(3):68. doi: 10.1007/s10555-025-10287-x.

DOI:10.1007/s10555-025-10287-x
PMID:40926108
Abstract

Integrins constitute a large and diverse family of cell adhesion molecules that play essential roles in regulating tumor cell differentiation, migration, proliferation, and neovascularization. Tumor cell-derived exosomes, a subtype of extracellular vesicles, are enriched with integrins that reflect their cells of origin. These exosomal integrins can promote extracellular matrix remodeling, immune suppression, and vascular remodeling and are closely linked to tumor progression and metastasis, acting as pivotal players in mediating organ-specific metastasis. The present review aims to discuss recent insights into the role of integrins from extracellular vesicles in tumor cell initiation, proliferation, migration, and invasion. Beyond their functional roles in cancer progression, exosomal integrins hold relevant potential as diagnostic and prognostic biomarkers due to their tissue-specific expression patterns. They also represent promising therapeutic targets for disrupting tumor-stroma interactions and preventing metastatic spread. As research into exosomal integrins continues to expand, they are likely to provide valuable insights into cancer biology and innovative strategies in cancer diagnosis and treatment.

摘要

整合素构成了一个庞大且多样的细胞黏附分子家族,在调节肿瘤细胞分化、迁移、增殖和新血管形成中发挥着重要作用。肿瘤细胞衍生的外泌体是细胞外囊泡的一种亚型,富含反映其起源细胞的整合素。这些外泌体整合素可促进细胞外基质重塑、免疫抑制和血管重塑,并与肿瘤进展和转移密切相关,在介导器官特异性转移中起关键作用。本综述旨在探讨细胞外囊泡中的整合素在肿瘤细胞起始、增殖、迁移和侵袭中的作用的最新见解。除了在癌症进展中的功能作用外,外泌体整合素因其组织特异性表达模式而具有作为诊断和预后生物标志物的相关潜力。它们还代表了破坏肿瘤-基质相互作用和预防转移扩散的有前景的治疗靶点。随着对外泌体整合素的研究不断扩展,它们可能会为癌症生物学以及癌症诊断和治疗的创新策略提供有价值的见解。

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本文引用的文献

1
Cancer-associated fibroblast-derived extracellular vesicles: regulators and therapeutic targets in the tumor microenvironment.癌症相关成纤维细胞衍生的细胞外囊泡:肿瘤微环境中的调节因子和治疗靶点
Cancer Drug Resist. 2025 Jan 7;8:2. doi: 10.20517/cdr.2024.152. eCollection 2025.
2
Vinculin-Arp2/3 interaction inhibits branched actin assembly to control migration and proliferation. vinculin-Arp2/3 相互作用抑制分支状肌动蛋白组装以控制迁移和增殖。
Life Sci Alliance. 2024 Nov 15;8(2). doi: 10.26508/lsa.202402583. Print 2025 Feb.
3
Exosomal integrins in tumor progression, treatment and clinical prediction (Review).
外泌体整合素在肿瘤进展、治疗和临床预测中的作用(综述)。
Int J Oncol. 2024 Dec;65(6). doi: 10.3892/ijo.2024.5706. Epub 2024 Nov 14.
4
Talin and vinculin combine their activities to trigger actin assembly.塔林和纽蛋白结合它们的活性来触发肌动蛋白组装。
Nat Commun. 2024 Nov 3;15(1):9497. doi: 10.1038/s41467-024-53859-1.
5
Recycling machinery of integrin coupled with focal adhesion turnover via RAB11-UNC13D-FAK axis for migration of pancreatic cancer cells.整合素偶联的循环机械装置通过 RAB11-UNC13D-FAK 轴促进胰腺癌细胞迁移。
J Transl Med. 2024 Aug 29;22(1):800. doi: 10.1186/s12967-024-05630-9.
6
Biophysical aspects of migrasome organelle formation and their diverse cellular functions.迁移体细胞器形成的生物物理方面及其多种细胞功能。
Bioessays. 2024 Aug;46(8):e2400051. doi: 10.1002/bies.202400051. Epub 2024 Jun 23.
7
Migrasome, a migration-dependent organelle.迁移小体,一种依赖于迁移的细胞器。
Front Cell Dev Biol. 2024 Jun 6;12:1417242. doi: 10.3389/fcell.2024.1417242. eCollection 2024.
8
Novel insights into the roles of migrasome in cancer.对迁移体在癌症中作用的新见解。
Discov Oncol. 2024 May 15;15(1):166. doi: 10.1007/s12672-024-00942-0.
9
Zearalenone Induces Blood-Testis Barrier Damage through Endoplasmic Reticulum Stress-Mediated Paraptosis of Sertoli Cells in Goats.玉米赤霉烯酮通过内质网应激介导的山羊支持细胞副凋亡诱导血睾屏障损伤。
Int J Mol Sci. 2023 Dec 31;25(1):553. doi: 10.3390/ijms25010553.
10
Migrasome: a new functional extracellular vesicle.迁移体:一种新型功能性细胞外囊泡。
Cell Death Discov. 2023 Oct 18;9(1):381. doi: 10.1038/s41420-023-01673-x.