胶质母细胞瘤血管系统:从其在肿瘤存活中的关键作用到相关的体外建模

Catarina C. Pacheco, Cláudia Martins, J. Monteiro, F. Baltazar, B. Costa, B. Sarmento
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引用次数: 2

摘要

控制胶质母细胞瘤(GBM)进展的生化和生物物理线索是复杂和动态的。肿瘤血管通常仅通过其运输功能来识别,但它们更深入地参与了这一过程。血管参与肿瘤免疫逃避、基质改变和干细胞刺激,是肿瘤治疗耐药和患者生存差的原因之一。由于血管的复杂性和动态性,它们很难在传统的GBM单层体外模型中表现出来。然而,其他体外方法,如三维(3D)模型,结合细胞外基质(ECM)、恶性细胞和基质细胞,并促进它们的交流,可以在类似肿瘤的微环境中类似于新生血管的生长。这些模型模拟了GBM的生理结构和关键的生化和生物物理环境,允许研究血管化在肿瘤进展中的影响。神经肿瘤学领域的研究人员对三维血管化GBM模型非常感兴趣。它们是评估个体驱动的新生血管形成和识别这些过程中涉及的介质的有前途的工具。此外,它们可用于测试针对血管或受其影响的潜在抗gbm疗法。本文将讨论血管在GBM中的意义,并综述新的三维临床前血管模型。
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Glioblastoma Vasculature: From its Critical Role in Tumor Survival to Relevant in Vitro Modelling
Biochemical and biophysical cues governing glioblastoma (GBM) progression are complex and dynamic. Tumor blood vessels, often recognized only by their transport functions, are more deeply involved in this process. Vessels are involved in tumor immune evasion, matrix alterations and stem cell stimulation, contributing for tumor treatment resistance and patients’ poor survival. Given blood vessel complex and dynamic nature, they are hardly represented in conventional GBM monolayered in vitro models. However, other in vitro approaches, such as three-dimensional (3D) models, incorporating extracellular matrix (ECM), malignant and stromal cells, and promoting their communication, can resemble neovascularization, growing blood vessels in a tumor-like microenvironment. These models mimic GBM physiological architecture and key biochemical and biophysical environments, allowing the investigation of the impact of vascularization in tumor progression. For researchers in neuro-oncology field, 3D vascularized GBM models are of great interest. They are promising tools to evaluate individual driven neovascularization and identify mediators involved in those processes. Moreover, they may be used to test potential anti-GBM therapies targeting blood vessels or influenced by them. This review will discuss the significance of blood vessels in GBM and review novel 3D pre-clinical vascular models.
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