Chorom Pak , Kaylene J. Simpson , Andrea D. Weston , Mary Ellen Cvijic , Kenda Evans , Andrew D. Napper
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引用次数: 0
摘要
在此,我们根据 2023 年 SLAS 大会筛选设计和检测技术特别兴趣小组会议上题为 "表型筛选、靶点 ID 和多组学:在早期发现中实现更多疾病相关性?会议期间,作者们分享了各自组织内的经验,随后与听众进行了开放式讨论。大家认识到,虽然在将疾病相关的表型早期发现转化为临床成功方面取得了重大进展,但在实施表型筛选工作方面仍存在重大的操作和科学挑战,而且提高筛选结果的转化需要大量的资源需求和组织承诺。本视角评估了进展情况,强调了陷阱,并提供了可能的解决方案,以帮助释放表型药物发现的治疗潜力。探讨的领域包括筛选和新药验证策略、细胞模型的选择、从二维细胞培养到三维细胞培养,以及利用表型筛选下游的高维数据集。
Perspectives on phenotypic screening−Screen Design and Assay Technology Special Interest Group
Here we offer perspectives on phenotypic screening based on a wide-ranging discussion entitled “Phenotypic screening, target ID, and multi-omics: enabling more disease relevance in early discovery?” at the Screen Design and Assay Technology Special Interest Group Meeting at the 2023 SLAS Conference. During the session, the authors shared their own experience from within their respective organizations, followed by an open discussion with the audience. It was recognized that while substantial progress has been made towards translating disease-relevant phenotypic early discovery into clinical success, there remain significant operational and scientific challenges to implementing phenotypic screening efforts, and improving translation of screening hits comes with substantial resource demands and organizational commitment. This Perspective assesses progress, highlights pitfalls, and offers possible solutions to help unlock the therapeutic potential of phenotypic drug discovery. Areas explored comprise screening and hit validation strategy, choice of cellular model, moving beyond 2D cell culture into three dimensions, and leveraging high-dimensional data sets downstream of phenotypic screens.