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本文引用的文献

1
Reproducibility of Uniform Spheroid Formation in 384-Well Plates: The Effect of Medium Evaporation.384孔板中均匀球体形成的可重复性:培养基蒸发的影响。
J Biomol Screen. 2016 Oct;21(9):923-30. doi: 10.1177/1087057116651867. Epub 2016 May 25.
2
Development of an in vitro tumor spheroid culture model amenable to high-throughput testing of potential anticancer nanotherapeutics.开发一种适用于潜在抗癌纳米治疗药物高通量测试的体外肿瘤球体培养模型。
J Liposome Res. 2016 Sep;26(3):246-60. doi: 10.3109/08982104.2015.1105820. Epub 2016 Jan 18.
3
3D tumor spheroid models for in vitro therapeutic screening: a systematic approach to enhance the biological relevance of data obtained.用于体外治疗筛选的3D肿瘤球体模型:一种增强所获数据生物学相关性的系统方法。
Sci Rep. 2016 Jan 11;6:19103. doi: 10.1038/srep19103.
4
High-content assays for characterizing the viability and morphology of 3D cancer spheroid cultures.用于表征3D癌症球体培养物的活力和形态的高内涵分析。
Assay Drug Dev Technol. 2015 Sep;13(7):402-14. doi: 10.1089/adt.2015.655.
5
Improved Methods to Generate Spheroid Cultures from Tumor Cells, Tumor Cells & Fibroblasts or Tumor-Fragments: Microenvironment, Microvesicles and MiRNA.从肿瘤细胞、肿瘤细胞与成纤维细胞或肿瘤组织块生成球体培养物的改良方法:微环境、微泡和微小RNA
PLoS One. 2015 Jul 24;10(7):e0133895. doi: 10.1371/journal.pone.0133895. eCollection 2015.
6
Pathophysiologically relevant in vitro tumor models for drug screening.用于药物筛选的病理生理相关的体外肿瘤模型。
Drug Discov Today. 2015 Jul;20(7):848-55. doi: 10.1016/j.drudis.2015.04.004. Epub 2015 Apr 20.
7
High-throughput image analysis of tumor spheroids: a user-friendly software application to measure the size of spheroids automatically and accurately.肿瘤球体的高通量图像分析:一款用户友好型软件应用程序,可自动、准确地测量球体大小。
J Vis Exp. 2014 Jul 8(89):51639. doi: 10.3791/51639.
8
Optimization of liquid overlay technique to formulate heterogenic 3D co-cultures models.优化液体覆盖技术以构建异质性三维共培养模型。
Biotechnol Bioeng. 2014 Aug;111(8):1672-85. doi: 10.1002/bit.25210. Epub 2014 Feb 25.
9
3D high-content screening for the identification of compounds that target cells in dormant tumor spheroid regions.三维高内涵筛选鉴定靶向休眠肿瘤球区域细胞的化合物。
Exp Cell Res. 2014 Apr 15;323(1):131-143. doi: 10.1016/j.yexcr.2014.01.017. Epub 2014 Jan 27.
10
An imaging-based platform for high-content, quantitative evaluation of therapeutic response in 3D tumour models.一个基于成像的平台,用于对三维肿瘤模型中的治疗反应进行高内涵定量评估。
Sci Rep. 2014 Jan 17;4:3751. doi: 10.1038/srep03751.

降低蒸发的培养条件提高了微孔板中多细胞球体形成的可重复性。

Evaporation-reducing Culture Condition Increases the Reproducibility of Multicellular Spheroid Formation in Microtiter Plates.

作者信息

Das Viswanath, Fürst Tomáš, Gurská Soňa, Džubák Petr, Hajdúch Marián

机构信息

Institute of Molecular and Translational Medicine, Palacky University in Olomouc.

Institute of Molecular and Translational Medicine, Palacky University in Olomouc;

出版信息

J Vis Exp. 2017 Mar 7(121):55403. doi: 10.3791/55403.

DOI:10.3791/55403
PMID:28362402
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5408984/
Abstract

Tumor models that closely imitate in vivo conditions are becoming increasingly popular in drug discovery and development for the screening of potential anti-cancer drugs. Multicellular tumor spheroids (MCTSes) effectively mimic the physiological conditions of solid tumors, making them excellent in vitro models for lead optimization and target validation. Out of the various techniques available for MCTS culture, the liquid-overlay method on agarose is one of the most inexpensive methods for MCTS generation. However, the reliable transfer of MCTS cultures using liquid-overlay for high-throughput screening may be compromised by a number of limitations, including the coating of microtiter plates (MPs) with agarose and the irreproducibility of uniform MCTS formation across wells. MPs are significantly prone to edge effects that result from excessive evaporation of medium from the exterior of the plate, preventing the use of the entire plate for drug tests. This manuscript provides detailed technical improvements to the liquid-overlay technique to increase the scalability and reproducibility of uniform MCTS formation. Additionally, details on a simple, semi-automatic, and universally applicable software tool for the evaluation of MCTS features after drug treatment is presented.

摘要

在药物发现和开发过程中,用于筛选潜在抗癌药物的、能紧密模拟体内条件的肿瘤模型正变得越来越受欢迎。多细胞肿瘤球体(MCTS)能有效模拟实体瘤的生理条件,使其成为用于先导化合物优化和靶点验证的优秀体外模型。在可用于MCTS培养的各种技术中,琼脂糖上的液体覆盖法是生成MCTS最廉价的方法之一。然而,使用液体覆盖法进行MCTS培养以用于高通量筛选时,可靠的转移可能会受到许多限制的影响,包括用琼脂糖包被微孔板(MP)以及各孔间均匀形成MCTS的不可重复性。MP极易受到边缘效应的影响,这种边缘效应是由板外部培养基过度蒸发导致的,从而妨碍了将整个板用于药物测试。本手稿提供了对液体覆盖技术的详细技术改进,以提高均匀形成MCTS的可扩展性和可重复性。此外,还介绍了一种简单、半自动且普遍适用的软件工具的详细信息,该工具用于评估药物处理后MCTS的特征。