Experimental and Clinical Research Center, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Max-Delbrück-Center for Molecular Medicine, AG Translational Oncology of Solid Tumors, Berlin, Germany.
Methods Mol Biol. 2021;2294:133-142. doi: 10.1007/978-1-0716-1350-4_9.
Drug-mediated interference with metastasis represents a key approach to improve cancer therapy. In this regard, appropriate in vitro assays are needed to identify drugs, which inhibit cell migration as one feature for metastatic potential of cancer cells. One such migration assay is the wound healing or scratch assay, designed to allow cells for closure of an artificially generated gap (wound/scratch) in the monolayer. To identify possibly effective anti-migratory drugs as monotherapy or as synergistic drug combination, novel screening tools besides viability measurements at the experimental endpoint are needed. In this context, particularly drug combinations allow to increase treatment efficacy paralleled by lowered side effects. Here, a protocol for real-time monitoring cellular motility and its inhibition by anti-migratory drugs and combinations by the IncuCyte system and a 96-well scratch assay is described. A pipetting scheme allowing data collection for synergy calculation using one plate per replicate is provided. Using the IncuCyte System 2, drug combinations built of three biological replicates each using three technical replicates can be tested in parallel within hours to few days to accelerate identification of efficient antimetastatic drugs.
药物介导的转移干扰代表了改善癌症治疗的一种关键方法。在这方面,需要适当的体外检测方法来识别抑制细胞迁移的药物,因为这是癌细胞转移潜力的一个特征。划痕实验就是这样一种迁移检测方法,它旨在允许细胞封闭单层中人为产生的间隙(伤口/划痕)。为了鉴定可能有效的抗迁移药物作为单一疗法或协同药物组合,除了在实验终点进行生存力测量之外,还需要新的筛选工具。在这种情况下,药物组合特别允许在降低副作用的同时提高治疗效果。这里,描述了一种通过 IncuCyte 系统和 96 孔划痕实验实时监测细胞迁移及其被抗迁移药物和组合抑制的方案。提供了一种移液方案,允许使用每个重复的一个平板收集用于协同作用计算的数据。使用 IncuCyte System 2,每个生物重复构建三个技术重复的药物组合可以在数小时到数天内平行测试,以加速鉴定有效的抗转移药物。