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Patterning hypoxic multicellular spheroids in a 3D matrix - a promising method for anti-tumor drug screening

机译:在3D矩阵中对低氧多细胞球体进行图案化-一种抗肿瘤药物筛选的有前途的方法

摘要

3D multicellular spheroid models are of great value in the investigation of tumor biology and tumor responses to chemotherapy and radiation. To establish a mimicking tumor microenvironment in vitro, we developed a straightforward method by patterning hypoxic multicellular spheroids in a 3D matrix. The efficacy of this approach was evaluated by characterizing spheroid formation, invasive capability and phenotypic transition in aggressive human glioma cells. We observed enhanced cell proliferation, spheroid formation and invasive capability in U87 glioma cells transfected with hypoxia-inducible factors (HIFs) compared with non-treated cells. We also demonstrated that the overexpression of HIFs in hypoxic glioma cells may promote cell migration by epithelial-mesenchymal transition within the 3D matrix. Compared with conventional 3D culturing techniques, the simple operation, rapid prototyping, low cost and high throughput format of the micro-patterning method facilitates the characterization of cell proliferation, migration, phenotypic function and drug evaluation in physiologically relevant 3D microenvironments. This in vitro 3D system can recapitulate the physiologically relevant tumor microenvironment and is a promising method for 3D anti-tumor drug screening and the identification of novel targets for tumor invasion and angiogenesis.
机译:3D多细胞球体模型在研究肿瘤生物学以及肿瘤对化学疗法和放射线的反应方面具有重要价值。为了在体外建立模拟肿瘤的微环境,我们通过在3D矩阵中图案化缺氧的多细胞球体,开发了一种简单的方法。通过表征攻击性人类神经胶质瘤细胞中的球体形成,侵袭能力和表型转变,评估了该方法的有效性。我们观察到与未处理的细胞相比,用缺氧诱导因子(HIFs)转染的U87胶质瘤细胞增强了细胞增殖,球状体形成和侵袭能力。我们还证明了低氧神经胶质瘤细胞中HIF的过度表达可能通过3D基质内的上皮-间质转化促进细胞迁移。与传统的3D培养技术相比,微图案化方法的简单操作,快速成型,低成本和高通量格式,有助于在生理相关的3D微环境中表征细胞增殖,迁移,表型功能和药物评估。该体外3D系统可以概括生理相关的肿瘤微环境,是用于3D抗肿瘤药物筛选以及鉴定肿瘤侵袭和血管生成的新靶标的有前途的方法。

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