Das Viswanath, Fürst Tomáš, Gurská Soňa, Džubák Petr, Hajdúch Marián
Institute of Molecular and Translational Medicine, Palacky University in Olomouc.
Institute of Molecular and Translational Medicine, Palacky University in Olomouc;
J Vis Exp. 2017 Mar 7(121):55403. doi: 10.3791/55403.
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.
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。