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利用基于微孔的琼脂糖支架生成用于药物测试的多细胞肿瘤球体。

Generation of Multicellular Tumor Spheroids with Microwell-Based Agarose Scaffolds for Drug Testing.

作者信息

Gong Xue, Lin Chao, Cheng Jian, Su Jiansheng, Zhao Hang, Liu Tianlin, Wen Xuejun, Zhao Peng

机构信息

Laboratory of Oral Biomedical Science and Translational Medicine, Department of Prosthodontics, School of Stomatology, Tongji University, Shanghai, P.R. China.

Institute for Biomedical Engineering & Nano Science, Tongji University School of Medicine, Tongji University, Shanghai, P.R. China.

出版信息

PLoS One. 2015 Jun 19;10(6):e0130348. doi: 10.1371/journal.pone.0130348. eCollection 2015.

Abstract

Three dimensional multicellular aggregate, also referred to as cell spheroid or microtissue, is an indispensable tool for in vitro evaluating antitumor activity and drug efficacy. Compared with classical cellular monolayer, multicellular tumor spheroid (MCTS) offers a more rational platform to predict in vivo drug efficacy and toxicity. Nevertheless, traditional processing methods such as plastic dish culture with nonadhesive surfaces are regularly time-consuming, laborious and difficult to provide uniform-sized spheroids, thus causing poor reproducibility of experimental data and impeding high-throughput drug screening. In order to provide a robust and effective platform for in vitro drug evaluation, we present an agarose scaffold prepared with the template containing uniform-sized micro-wells in commercially available cell culture plates. The agarose scaffold allows for good adjustment of MCTS size and large-scale production of MCTS. Transparent agarose scaffold also allows for monitoring of spheroid formation under an optical microscopy. The formation of MCTS from MCF-7 cells was prepared using different-size-well templates and systematically investigated in terms of spheroid growth curve, circularity, and cell viability. The doxorubicin cytotoxicity against MCF-7 spheroid and MCF-7 monolayer cells was compared. The drug penetration behavior, cell cycle distribution, cell apoptosis, and gene expression were also evaluated in MCF-7 spheroid. The findings of this study indicate that, compared with cellular monolayer, MCTS provides a valuable platform for the assessment of therapeutic candidates in an in vivo-mimic microenvironment, and thus has great potential for use in drug discovery and tumor biology research.

摘要

三维多细胞聚集体,也称为细胞球状体或微组织,是体外评估抗肿瘤活性和药物疗效不可或缺的工具。与经典的细胞单层相比,多细胞肿瘤球状体(MCTS)为预测体内药物疗效和毒性提供了一个更合理的平台。然而,传统的处理方法,如在非粘性表面的塑料培养皿中培养,通常耗时、费力,且难以提供大小均匀的球状体,从而导致实验数据的重现性差,并阻碍高通量药物筛选。为了提供一个强大而有效的体外药物评估平台,我们展示了一种琼脂糖支架,它是在市售细胞培养板中用含有均匀尺寸微孔的模板制备的。琼脂糖支架能够很好地调节MCTS的大小并实现MCTS的大规模生产。透明的琼脂糖支架还允许在光学显微镜下监测球状体的形成。使用不同尺寸孔的模板制备了MCF-7细胞形成的MCTS,并从球状体生长曲线、圆形度和细胞活力方面进行了系统研究。比较了阿霉素对MCF-7球状体和MCF-7单层细胞的细胞毒性。还评估了MCF-7球状体中的药物渗透行为、细胞周期分布、细胞凋亡和基因表达。本研究结果表明,与细胞单层相比,MCTS为在体内模拟微环境中评估治疗候选物提供了一个有价值的平台,因此在药物发现和肿瘤生物学研究中具有巨大的应用潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/848b/4474551/c6d3cf0a2fd1/pone.0130348.g001.jpg

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