基于细胞筛选鉴定细胞保护化合物

Domokos Gerő
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引用次数: 1

摘要

预防细胞损伤和随之而来的细胞死亡有望为各种疾病提供治疗益处,但由于涉及细胞损伤途径的复杂性,鉴定和验证新的潜在药物靶点不是一项微不足道的任务。新的药物靶点有望参与复杂的反应,对基因表达和细胞功能产生广泛的影响,候选药物更愿意改变这些影响,而不是作为简单的激动剂或拮抗剂,最终保护细胞免受损伤。表型筛选可能有助于识别疾病中的细胞保护化合物,其中缺乏药物靶标使得基于靶标的方法不可行。本章概述了基于细胞的检测开发、初步筛选、命中选择和确认的策略。讨论了基于细胞的模型中使用的小分子化合物文库的选择以及临床药物用于药物再利用或重新定位的考虑。概述了细胞类型的选择和与细胞培养技术相关的问题,并简要描述了最常见的测定和读数。最后,讨论了数据分析和命中选择的潜在缺陷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cell-Based Screening to Identify Cytoprotective Compounds
Prevention of cellular injury and consequent cell death is expected to provide therapeutic benefit in various diseases, but with the complexity of cell damaging pathways involved, identification and validation of novel potential drug targets is not a trivial task. New drug targets are expected to take part in complex responses with wide-ranging effects on gene expression and cellular function and drug candidates rather modify these effects than act as simple agonists or antagonists to ultimately protect the cells from an injury. Phenotypic screening may help identify cytoprotective compounds in diseases, in which the lack of drug targets makes target-based approaches unfeasible. This chapter gives an overview of the strategy of cell-based assay development, primary screening, hit selection and confirmation. Considerations about the choice of small molecule compound libraries utilized in cell-based models are discussed as well as the use of clinical drugs for drug repurposing or repositioning. The choice of cell types and issues associated with cell culture techniques are overviewed and the most common assays and readouts are briefly described. Finally, the potential pitfalls of data analysis and hit selection are discussed.
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