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用于评估亚群特异性药物反应的多细胞类型胶质母细胞瘤肿瘤球体

Multi-Cell Type Glioblastoma Tumor Spheroids for Evaluating Sub-Population-Specific Drug Response.

作者信息

Sivakumar Hemamylammal, Devarasetty Mahesh, Kram David E, Strowd Roy E, Skardal Aleksander

机构信息

Department of Biomedical Engineering, The Ohio State University, Columbus, OH, United States.

The Ohio State University and Arthur G. James Comprehensive Cancer Center, Columbus, OH, United States.

出版信息

Front Bioeng Biotechnol. 2020 Sep 15;8:538663. doi: 10.3389/fbioe.2020.538663. eCollection 2020.

Abstract

Glioblastoma (GBM) is a lethal, incurable form of cancer in the brain. Even with maximally aggressive surgery and chemoradiotherapy, median patient survival is 14.5 months. These tumors infiltrate normal brain tissue, are surgically incurable, and universally recur. GBMs are characterized by genetic, epigenetic, and microenvironmental heterogeneity, and they evolve spontaneously over time and as a result of treatment. However, tracking such heterogeneity in real time in response to drug treatments has been impossible. Here we describe the development of an GBM tumor organoid model that is comprised of five distinct cellular subpopulations (4 GBM cell lines that represent GBM subpopulations and 1 astrocyte line), each fluorescently labeled with a different color. These multi-cell type GBM organoids are then embedded in a brain-like hyaluronic acid hydrogel for subsequent studies involving drug treatments and tracking of changes in relative numbers of each fluorescently unique subpopulation. This approach allows for the visual assessment of drug influence on individual subpopulations within GBM, and in future work can be expanded to supporting studies using patient tumor biospecimen-derived cells for personalized diagnostics.

摘要

胶质母细胞瘤(GBM)是一种致命的、无法治愈的脑癌。即使进行最大程度的积极手术及放化疗,患者的中位生存期也仅为14.5个月。这些肿瘤会浸润正常脑组织,无法通过手术治愈,且普遍会复发。GBM具有基因、表观遗传和微环境异质性,会随着时间推移以及治疗而自发演变。然而,实时追踪药物治疗引发的这种异质性一直无法实现。在此,我们描述了一种GBM肿瘤类器官模型的构建,该模型由五个不同的细胞亚群组成(代表GBM亚群的4种GBM细胞系和1种星形胶质细胞系),每个亚群都用不同颜色进行荧光标记。然后将这些多细胞类型的GBM类器官嵌入类似脑的透明质酸水凝胶中,用于后续涉及药物治疗以及追踪每个荧光独特亚群相对数量变化的研究。这种方法能够直观评估药物对GBM内各个亚群的影响,并且在未来的研究中,可以扩展到使用患者肿瘤生物标本衍生细胞进行个性化诊断的支持性研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b38f/7523412/aedeef0bbc32/fbioe-08-538663-g001.jpg

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