Three-dimensional culture models to study glioblastoma — current trends and future perspectives

清脆的 胶质母细胞瘤 生命银行 基因组编辑 生物 计算生物学 肿瘤微环境 神经科学 转化研究 个性化医疗 类有机物 免疫系统 生物信息学 癌症研究 基因 免疫学 生物技术 遗传学
作者
Justin V. Joseph,Mathilde S. Blaavand,Thomas Daubon,Frank A.E. Kruyt,Martin K. Thomsen
出处
期刊:Current Opinion in Pharmacology [Elsevier]
卷期号:61: 91-97 被引量:11
标识
DOI:10.1016/j.coph.2021.08.019
摘要

Glioblastoma (GBM) is the most prevalent form of primary malignant brain tumor in adults and remains almost invariably lethal owing to its aggressive and invasive nature. There have only been marginal improvements in its bleak survival rate of 12-15 months over the last four decades. The lack of preclinical models that efficiently recapitulate tumor biology and the tumor microenvironment is also in part responsible for the slow phase of translational GBM research. Emerging three-dimensional (3D) organoids and cell culture systems offer new and innovative possibilities for GBM modelling. These 3D models find their application to engineer the disease, screen drugs, establishing live biobank, and explore personalized therapy. Furthermore, these models can also be genetically modified by using the clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 technology, which would allow one to study the specific role of key genes associated with gliomagenesis. Establishment of a coculture system with GBM cells to understand its invasive behavior is yet another major application of this model. Despite these merits, the organoid models also have certain limitations, including the absence of immune responses and vascular systems. In recent years, major progress has been made in the development and refinement of 3D models of GBM. In this review, we intend to highlight these recent advances and the potential future implications of this rapidly evolving field, which should facilitate a better understanding of GBM biology.
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