Suppr超能文献

一种用于定义肿瘤与间充质干细胞之间细胞外囊泡介导通讯的骨肉瘤临床前小鼠模型。

A Preclinical Mouse Model of Osteosarcoma to Define the Extracellular Vesicle-mediated Communication Between Tumor and Mesenchymal Stem Cells.

作者信息

Lagerweij Tonny, Pérez-Lanzón Maria, Baglio S Rubina

机构信息

Neuro-oncology Research Group, VU Medical Center.

Exosomes Research Group, Department of Pathology, VU Medical Center.

出版信息

J Vis Exp. 2018 May 6(135):56932. doi: 10.3791/56932.

Abstract

Within the tumor microenvironment, resident or recruited mesenchymal stem cells (MSCs) contribute to malignant progression in multiple cancer types. Under the influence of specific environmental signals, these adult stem cells can release paracrine mediators leading to accelerated tumor growth and metastasis. Defining the crosstalk between tumor and MSCs is of primary importance to understand the mechanisms underlying cancer progression and identify novel targets for therapeutic intervention. Cancer cells produce high amounts of extracellular vesicles (EVs), which can profoundly affect the behavior of target cells in the tumor microenvironment or at distant sites. Tumor EVs enclose functional biomolecules, including inflammatory RNAs and (onco)proteins, that can educate stromal cells to enhance the metastatic behavior of cancer cells or to participate in the pre-metastatic niche formation. In this article, we describe the development of a preclinical cancer mouse model that enables specific evaluation of the EV-mediated crosstalk between tumor and mesenchymal stem cells. First, we describe the purification and characterization of tumor-secreted EVs and the assessment of the EV internalization by MSCs. We then make use of a multiplex bead-based immunoassay to evaluate the alteration of the MSC cytokine expression profile induced by cancer EVs. Finally, we illustrate the generation of a bioluminescent orthotopic xenograft mouse model of osteosarcoma that recapitulates the tumor-MSC interaction, and show the contribution of EV-educated MSCs to tumor growth and metastasis formation. Our model provides the opportunity to define how cancer EVs shape a tumor-supporting environment, and to evaluate whether blockade of the EV-mediated communication between tumor and MSCs prevents cancer progression.

摘要

在肿瘤微环境中,驻留或募集的间充质干细胞(MSC)在多种癌症类型中促进恶性进展。在特定环境信号的影响下,这些成体干细胞可释放旁分泌介质,导致肿瘤生长加速和转移。明确肿瘤与MSC之间的相互作用对于理解癌症进展的潜在机制以及确定治疗干预的新靶点至关重要。癌细胞产生大量细胞外囊泡(EV),其可深刻影响肿瘤微环境中或远处靶细胞的行为。肿瘤EV包裹着功能性生物分子,包括炎性RNA和(癌)蛋白,这些分子可影响基质细胞,增强癌细胞转移行为或参与前转移生态位的形成。在本文中,我们描述了一种临床前癌症小鼠模型的构建,该模型能够特异性评估EV介导的肿瘤与间充质干细胞之间的相互作用。首先我们描述肿瘤分泌EV的纯化和表征以及MSC对EV的内化评估。然后我们利用基于多重磁珠的免疫测定法评估癌症EV诱导的MSC细胞因子表达谱的变化。最后,我们展示了一种骨肉瘤生物发光原位异种移植小鼠模型的构建,该模型概括了肿瘤与MSC的相互作用,并展示了受过EV影响的MSC对肿瘤生长和转移形成的作用。我们的模型提供了一个机会,来明确癌症EV如何塑造肿瘤支持环境,并评估阻断EV介导肿瘤与MSC之间的通讯是否能阻止癌症进展。

相似文献

引用本文的文献

1
Advances on immunotherapy for osteosarcoma.骨肉瘤的免疫治疗进展。
Mol Cancer. 2024 Sep 9;23(1):192. doi: 10.1186/s12943-024-02105-9.
6
Functions and therapeutic potentials of exosomes in osteosarcoma.骨肉瘤中外泌体的功能及治疗潜力
Acta Mater Med. 2022 Oct 18;1(4):552-562. doi: 10.15212/amm-2022-0024. Epub 2022 Dec 30.
8
Role of extracellular vesicles in osteosarcoma.细胞外囊泡在骨肉瘤中的作用。
Int J Med Sci. 2022 Jul 4;19(8):1216-1226. doi: 10.7150/ijms.74137. eCollection 2022.

本文引用的文献

9
Tumour exosome integrins determine organotropic metastasis.肿瘤外泌体整合素决定器官特异性转移。
Nature. 2015 Nov 19;527(7578):329-35. doi: 10.1038/nature15756. Epub 2015 Oct 28.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验