胶质母细胞瘤
串扰
U87型
脑瘤
癌症研究
肿瘤微环境
体外
肿瘤进展
生物
神经科学
肿瘤细胞
癌症
医学
病理
物理
光学
生物化学
遗传学
作者
Marcel Alexander Heinrich,Ruchi Bansal,Twan Lammers,Yu Shrike Zhang,Raymond M. Schiffelers,Jai Prakash
标识
DOI:10.1002/adma.201806590
摘要
Abstract Glioblastoma‐associated macrophages (GAMs) play a crucial role in the progression and invasiveness of glioblastoma multiforme (GBM); however, the exact crosstalk between GAMs and glioblastoma cells is not fully understood. Furthermore, there is a lack of relevant in vitro models to mimic their interactions. Here, novel 3D‐bioprinted mini‐brains consisting of glioblastoma cells and macrophages are presented as tool to study the interactions between these two cell types and to test therapeutics that target this interaction. It is demonstrated that in the mini‐brains, glioblastoma cells actively recruit macrophages and polarize them into a GAM‐specific phenotype, showing clinical relevance to transcriptomic and patient survival data. Furthermore, it is shown that macrophages induce glioblastoma cell progression and invasiveness in the mini‐brains. Finally, it is demonstrated how therapeutics can inhibit the interaction between GAMs and tumor cells resulting in reduced tumor growth and more sensitivity to chemotherapy. It is envisioned that this 3D‐bioprinted tumor model is used to improve the understanding of tumor biology and for evaluating novel cancer therapeutics.
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