肿瘤微环境
骨肉瘤
背景(考古学)
癌症
转移
癌症研究
肺癌
医学
体内
药物发现
肿瘤进展
肿瘤发生
癌细胞
计算生物学
原发性肿瘤
生物
生物信息学
病理
内科学
遗传学
古生物学
作者
J Rodrigues,Bruno Sarmento,Catarina Leite Pereira
出处
期刊:In vitro models
[Springer Nature]
日期:2022-01-18
卷期号:1 (1): 5-27
被引量:14
标识
DOI:10.1007/s44164-022-00008-x
摘要
Osteosarcoma (OS) is the most common primary bone cancer in children and young adults. This type of cancer is characterized by a high mortality rate, especially for patients with resistant lung metastases. Given its low incidence, high genetic heterogeneity, the lack of effective targets, and poor availability of relevant in vitro and in vivo models to study the tumor progression and the metastatic cascade, the pathophysiology of OS is still poorly understood and the translation of novel drugs into the market has become stagnant. Due to the importance of the tumor microenvironment (TME) in the development of metastases and the growing interest in targeting TME-specific pathways for novel therapeutics in cancer, models that closely represent these interactions are crucial for a better understanding of cancer-related events. In OS research, most studies rely on oversimplified two-dimensional (2D) assays and complex animal models that do not faithfully recapitulate OS development and progression. In turn, three-dimensional (3D) models are able to mimic not only the physical 3D environment in which cancer cells grow but also involve interactions with the TME, including its extracellular matrix, and thus are promising tools for drug screening studies. In this review, the existing and innovative OS in vitro 3D models are highlighted, focusing on how the TME is crucial to develop effective platforms for OS tumor and metastasis modeling in a physiologically relevant context.
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