Margarida F. Domingues, João C. Silva, Paola Sanjuan-Alberte
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引用次数: 0
摘要
骨肉瘤(Osteosarcoma,OS)是一种罕见的原发性恶性骨癌,主要影响年轻人。治疗方法通常包括化疗和手术切除肿瘤,但自 20 世纪 70 年代以来,化疗和手术切除肿瘤的方法鲜有改进。由于肿瘤固有的化疗抗药性、明显的异质性和转移潜力,这种治疗方法遇到了一些限制。因此,开发近似操作系统病理生理学的体外平台对于了解肿瘤进展和发现有效的抗癌疗法至关重要。与二维单层培养和动物模型相反,三维体外平台在复制三维肿瘤宏观结构、细胞-细胞和细胞-细胞外基质相互作用方面大有可为。本综述概述了开发三维体外 OS 模型所采用的生物制造策略,强调了它们在复制 OS 不同方面以及改善 OS 抗癌研究和药物筛选方面的作用。本文探讨了各种三维体外模型,包括无支架模型和基于支架的模型,涵盖细胞球、水凝胶以及电纺纳米纤维、微流体装置和生物打印构建物等创新方法。通过研究每种模型类型的显著特点,本综述深入探讨了它们对操作系统研究和治疗创新的潜在变革性影响,探讨了三维体外操作系统建模的挑战和未来方向。
From Spheroids to Bioprinting: A Literature Review on Biomanufacturing Strategies of 3D In Vitro Osteosarcoma Models
Osteosarcoma (OS) is a rare primary malignant bone cancer affecting mainly young individuals. Treatment typically consists of chemotherapy and surgical tumor resection, which has undergone few improvements since the 1970s. This therapeutic approach encounters several limitations attributed to the tumor's inherent chemoresistance, marked heterogeneity and metastatic potential. Therefore, the development of in vitro platforms that closely mimic the OS pathophysiology is crucial to understand tumor progression and discover effective anticancer therapeutics. Contrary to 2D monolayer cultures and animal models, 3D in vitro platforms show promise in replicating the 3D tumor macrostructure, cell-cell and cell-extracellular matrix interactions. This review provides an overview of the biomanufacturing strategies employed in developing 3D in vitro OS models, highlighting their role in replicating different aspects of OS and improving OS anticancer research and drug screening. A variety of 3D in vitro models are explored, including both scaffold-free and scaffold-based models, encompassing cell spheroids, hydrogels, and innovative approaches like electrospun nanofibers, microfluidic devices and bioprinted constructs. By examining the distinctive features of each model type, this review offers insights into their potential transformative impact on the landscape of OS research and therapeutic innovation, addressing the challenges and future directions of 3D in vitro OS modeling.