高通量方法揭示白血病的协同药物组合

IF 2.7 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Emma J. Chory , Meng Wang , Michele Ceribelli , Aleksandra M Michalowska , Stefan Golas , Erin Beck , Carleen Klumpp-Thomas , Lu Chen , Crystal McKnight , Zina Itkin , Kelli M. Wilson , David Holland , Sanjay Divakaran , James Bradner , Javed Khan , Berkley E. Gryder , Craig J. Thomas , Benjamin Z. Stanton
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引用次数: 0

摘要

我们报道了一项针对急性髓细胞白血病(AML)的综合药物协同作用研究。在这项工作中,我们研究了一组横跨MLL重排和非重排亚型的细胞系。这项工作包括一个社区资源,包括许多无法先验预测的协同药物组合,以及用于自动化和分析的开源代码。我们将药物协同作用的定义建立在Chou-Talalay方法的基础上,该方法有助于在等辐射图和中值效应图等表示中可视化协同作用实验。我们的主要发现包括影响染色质状态的药物协同作用,特别是在组蛋白H3赖氨酸-27修饰状态的调节方面。我们报告了开源高通量方法,这样就可以使用大多数实验室都可以使用的设备来完成多维药物筛选。这项研究将使人们能够对致命的癌症中的新药组合进行临床前研究,并向社区免费提供数据分析和自动化工作流程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

High-throughput approaches to uncover synergistic drug combinations in leukemia

High-throughput approaches to uncover synergistic drug combinations in leukemia

We report a comprehensive drug synergy study in acute myeloid leukemia (AML). In this work, we investigate a panel of cell lines spanning both MLL-rearranged and non-rearranged subtypes. The work comprises a resource for the community, with many synergistic drug combinations that could not have been predicted a priori, and open source code for automation and analyses. We base our definitions of drug synergy on the Chou-Talalay method, which is useful for visualizations of synergy experiments in isobolograms, and median-effects plots, among other representations. Our key findings include drug synergies affecting the chromatin state, specifically in the context of regulation of the modification state of histone H3 lysine-27. We report open source high throughput methodology such that multidimensional drug screening can be accomplished with equipment that is accessible to most laboratories. This study will enable preclinical investigation of new drug combinations in a lethal blood cancer, with data analysis and automation workflows freely available to the community.

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来源期刊
SLAS Discovery
SLAS Discovery Chemistry-Analytical Chemistry
CiteScore
7.00
自引率
3.20%
发文量
58
审稿时长
39 days
期刊介绍: Advancing Life Sciences R&D: SLAS Discovery reports how scientists develop and utilize novel technologies and/or approaches to provide and characterize chemical and biological tools to understand and treat human disease. SLAS Discovery is a peer-reviewed journal that publishes scientific reports that enable and improve target validation, evaluate current drug discovery technologies, provide novel research tools, and incorporate research approaches that enhance depth of knowledge and drug discovery success. SLAS Discovery emphasizes scientific and technical advances in target identification/validation (including chemical probes, RNA silencing, gene editing technologies); biomarker discovery; assay development; virtual, medium- or high-throughput screening (biochemical and biological, biophysical, phenotypic, toxicological, ADME); lead generation/optimization; chemical biology; and informatics (data analysis, image analysis, statistics, bio- and chemo-informatics). Review articles on target biology, new paradigms in drug discovery and advances in drug discovery technologies. SLAS Discovery is of particular interest to those involved in analytical chemistry, applied microbiology, automation, biochemistry, bioengineering, biomedical optics, biotechnology, bioinformatics, cell biology, DNA science and technology, genetics, information technology, medicinal chemistry, molecular biology, natural products chemistry, organic chemistry, pharmacology, spectroscopy, and toxicology. SLAS Discovery is a member of the Committee on Publication Ethics (COPE) and was published previously (1996-2016) as the Journal of Biomolecular Screening (JBS).
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