Ming Wenyu, Ma Wenzhen, Chen Lisa H, Volk Catherine, Michael Mervyn Dodson, Xu Yanping, Zhang Fang, Wang Xiaojun
Endocrine and Cardiovascular Research Division, Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, USA.
Assay Drug Dev Technol. 2013 Jul;11(6):388-95. doi: 10.1089/adt.2013.513.
Retinoic acid, the active metabolite of vitamin A, plays important roles in various physiological and pathological processes. The two-step production of retinoic acid from vitamin A (retinol) is catalyzed by alcohol dehydrogenases and aldehyde dehydrogenases, which are potential therapeutic targets for numerous diseases, such as obesity, diabetes, and cancer. Currently, the lack of a suitable high-throughput cellular assay hinders efforts to identify therapeutic small molecular inhibitors of aldehyde dehydrogenase, such as ALDH1A1. In this report, we utilized high-content imaging technology and a commercially available cell permeable ALDH substrate to develop a 96-well cellular ALDH1A1 assay. This assay has a robust and sensitive readout and is amenable to automation. With this cellular assay, we identified potent selective ALDH1A1 inhibitors to explore the role of retinoic acid production in various preclinical disease models.
视黄酸是维生素A的活性代谢产物,在各种生理和病理过程中发挥重要作用。从维生素A(视黄醇)两步生成视黄酸的过程由醇脱氢酶和醛脱氢酶催化,这些酶是肥胖、糖尿病和癌症等多种疾病的潜在治疗靶点。目前,缺乏合适的高通量细胞检测方法阻碍了鉴定醛脱氢酶(如ALDH1A1)治疗性小分子抑制剂的努力。在本报告中,我们利用高内涵成像技术和一种市售的细胞可渗透ALDH底物开发了一种96孔细胞ALDH1A1检测方法。该检测方法具有强大且灵敏的读数,并且适合自动化操作。通过这种细胞检测方法,我们鉴定出了有效的选择性ALDH1A1抑制剂,以探索视黄酸生成在各种临床前疾病模型中的作用。