Department of Chemistry, CICECO - Aveiro Institute of Materials, University of Aveiro, Campus Universitário de Santiago, 3810-193 Aveiro, Portugal.
Department of Chemistry, CICECO - Aveiro Institute of Materials, University of Aveiro, Campus Universitário de Santiago, 3810-193 Aveiro, Portugal.
Acta Biomater. 2018 Jul 15;75:11-34. doi: 10.1016/j.actbio.2018.05.034. Epub 2018 May 23.
Three-dimensional multicellular tumor models are receiving an ever-growing focus as preclinical drug-screening platforms due to their potential to recapitulate major physiological features of human tumors in vitro. In line with this momentum, the technologies for assembly of 3D microtumors are rapidly evolving towards a comprehensive inclusion of tumor microenvironment elements. Customized spherically structured platforms, including microparticles and microcapsules, provide a robust and scalable technology to imprint unique biomolecular tumor microenvironment hallmarks into 3D in vitro models. Herein, a comprehensive overview of novel advances on the integration of tumor-ECM components and biomechanical cues into 3D in vitro models assembled in spherical shaped platforms is provided. Future improvements regarding spatiotemporal/mechanical adaptability, and degradability, during microtumors in vitro 3D culture are also critically discussed considering the realistic potential of these platforms to mimic the dynamic tumor microenvironment. From a global perspective, the production of 3D multicellular spheroids with tumor ECM components included in spherical models will unlock their potential to be used in high-throughput screening of therapeutic compounds. It is envisioned, in a near future, that a combination of spherically structured 3D microtumor models with other advanced microfluidic technologies will properly recapitulate the flow dynamics of human tumors in vitro.
The ability to correctly mimic the complexity of the tumor microenvironment in vitro is a key aspect for the development of evermore realistic in vitro models for drug-screening and fundamental cancer biology studies. In this regard, conventional spheroid-based 3D tumor models, combined with spherically structured biomaterials, opens the opportunity to precisely recapitulate complex cell-extracellular matrix interactions and tumor compartmentalization. This review provides an in-depth focus on current developments regarding spherically structured scaffolds engineered into in vitro 3D tumor models, and discusses future advances toward all-encompassing platforms that may provide an improved in vitro/in vivo correlation in a foreseeable future.
由于三维多细胞肿瘤模型具有在体外重现人类肿瘤主要生理特征的潜力,因此作为临床前药物筛选平台,它们越来越受到关注。顺应这一发展趋势,用于组装三维微肿瘤的技术正迅速发展,全面纳入肿瘤微环境元素。定制的球形结构平台,包括微球和微胶囊,为将独特的生物分子肿瘤微环境特征印迹到三维体外模型中提供了强大且可扩展的技术。本文全面概述了将肿瘤细胞外基质成分和生物力学线索整合到球形平台组装的三维体外模型中的最新进展。还从这些平台模拟动态肿瘤微环境的实际潜力的角度,批判性地讨论了在微肿瘤体外三维培养过程中,时空/机械适应性和可降解性方面的未来改进。从全球角度来看,在包含肿瘤细胞外基质成分的球形模型中生产具有三维多细胞球体的能力将释放其用于治疗化合物高通量筛选的潜力。可以预见,在不久的将来,球形结构的 3D 微肿瘤模型与其他先进的微流控技术的结合将能够正确模拟人类肿瘤的体外流动动力学。
在体外正确模拟肿瘤微环境的复杂性是开发用于药物筛选和基础癌症生物学研究的更真实体外模型的关键方面。在这方面,结合球形生物材料的传统基于球体的 3D 肿瘤模型为精确再现复杂的细胞-细胞外基质相互作用和肿瘤区室化提供了机会。本综述深入关注了当前关于工程化到体外 3D 肿瘤模型中的球形结构支架的最新进展,并讨论了未来朝着全面涵盖平台的进展,这些平台可能在可预见的未来提供改进的体外/体内相关性。