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使用 Celigo 图像细胞仪对 3D 多细胞肿瘤球体进行实时细胞凋亡和活力高通量筛选。

Real-Time Apoptosis and Viability High-Throughput Screening of 3D Multicellular Tumor Spheroids Using the Celigo Image Cytometer.

机构信息

1 Department of Technology R&D, Nexcelom Bioscience LLC, Lawrence, MA, USA.

出版信息

SLAS Discov. 2018 Feb;23(2):202-210. doi: 10.1177/2472555217731076. Epub 2017 Sep 15.

Abstract

Three-dimensional tumor spheroid models have been increasingly used to investigate and characterize cancer drug compounds. Previously, the Celigo image cytometer has demonstrated its utility in a high-throughput screening manner for evaluating potential drug candidates in a 3D multicellular tumor spheroid (MCTS) primary screen. In addition, we have developed real-time kinetic caspase 3/7 apoptosis and propidium iodide viability 3D MCTS assays, both of which can be used in a secondary screen to better characterize the hit compounds. In this work, we monitored the kinetic apoptotic and cytotoxic effects of 14 compounds in 3D MCTS produced from the glioblastoma cell line U87MG in 384-well plates for 9 days. The kinetic results allowed the categorization of the effects from 14 drug compounds into early and late cytotoxic, apoptotic, cytostatic, and no effects. The real-time apoptosis and viability screening method can serve as an improved secondary screen to better understand the mechanism of action of these potential drug candidates identified from the primary screen, allowing one to identify a more qualified drug candidate and streamline the drug discovery process of research and development.

摘要

三维肿瘤球体模型已越来越多地被用于研究和表征癌症药物化合物。此前,Celigo 图像细胞仪已证明其在高通量筛选方面的实用性,可用于对 3D 多细胞肿瘤球体 (MCTS) 进行初步筛选,评估潜在的候选药物。此外,我们还开发了实时动力学 caspase 3/7 凋亡和碘化丙啶活力 3D MCTS 测定法,两者均可用于二次筛选,以更好地表征命中化合物。在这项工作中,我们在 384 孔板中监测了 14 种化合物在 U87MG 胶质母细胞瘤细胞系产生的 3D MCTS 中的动力学凋亡和细胞毒性作用,持续 9 天。动力学结果将 14 种药物化合物的作用分为早期和晚期细胞毒性、凋亡、细胞抑制和无作用。实时凋亡和活力筛选方法可用作改进的二次筛选,以更好地了解从初步筛选中鉴定出的这些潜在候选药物的作用机制,从而确定更合格的候选药物,并简化研究和开发的药物发现过程。

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