| Literature DB >> 30702785 |
Marcel Alexander Heinrich1, Ruchi Bansal1, Twan Lammers2, Yu Shrike Zhang3, Raymond Michel Schiffelers4, Jai Prakash1.
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.Entities:
Keywords: 3D bioprinting; drug screening; glioblastoma microenvironment; mini-brain; tumor-associated macrophages
Mesh:
Year: 2019 PMID: 30702785 DOI: 10.1002/adma.201806590
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849