转移模型:转移级联研究的工程方法

IF 5 Q1 ENGINEERING, BIOMEDICAL Progress in biomedical engineering (Bristol, England) Pub Date : 2020-10-21 DOI:10.1088/2516-1091/abc34f
Hawley C. Pruitt, S. Gerecht
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引用次数: 0

摘要

肿瘤的进展和转移需要肿瘤细胞和周围环境之间复杂的相互作用。传统的2D和3D组织培养模型缺乏精确模拟肿瘤微环境和转移级联的复杂性所需的精度和时空控制。生物医学工程的进步使我们能够产生精确和通用的模型系统来阐明肿瘤进展和转移的重要机制。新型生物材料的结合创造了一个特定的机械环境,促进了癌细胞机械转导的受控研究。此外,微流体装置不仅允许将流动和剪切力纳入血管化肿瘤模型,而且还阐明了癌细胞迁移的重要机制,改变了关于癌细胞启动转移模式的范式。在这里,我们回顾了生物医学工程方法模拟肿瘤微环境和转移级联的最新进展。我们讨论了这些方法如何推动了癌症生物学领域的发展,并增强了我们对肿瘤转移机制的理解。我们首先关注影响肿瘤细胞侵袭的初级微环境的物理和机械方面。然后我们使用肿瘤细胞外基质模型过渡到肿瘤细胞迁移,包括有限迁移。最后,我们回顾了内渗/外渗和继发部位定植的模型。
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Modeling metastasis: engineering approaches to study the metastatic cascade
Tumor progression and metastasis requires a complex interplay between tumor cells and their surrounding environment. Conventional 2D and 3D tissue culture models lack the precision and spatiotemporal control required to accurately model the complexity of the tumor microenvironment and metastatic cascade. Advances in biomedical engineering have allowed us to generate precise and versatile model systems to elucidate mechanisms vital to tumor progression and metastasis. The incorporation of novel biomaterials creates a specific mechanical environment that has facilitated controlled studies of cancer cell mechano-transduction. In addition, microfluidic devices have not only allowed for the incorporation of flow and shear forces into vascularized tumor models, but also elucidated vital mechanisms of cancer cell migration that have shifted paradigms about the mode in which cancer cells initiate metastasis. Here, we review the latest developments in biomedical engineering approaches to model the tumor microenvironment and metastatic cascade. We discuss how these approaches have advanced the field of cancer biology and enhanced our understanding of the mechanisms driving metastasis. We initially focus on physical and mechanical aspects of the primary microenvironment that impact tumor cell invasion. We then transition to tumor cell migration using models of tumor extracellular matrix including confined migration. Finally, we review models of intravasation/extravasation and colonization of secondary sites.
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CiteScore
9.40
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