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Development and validation of a higher throughput screening approach to genotoxicity testing using the GADD45a-GFP GreenScreen HC assay

机译:使用GaDD45a-GFp Greenscreen HC检测开发和验证更高通量的基因毒性检测方法

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摘要

There is a pressing need to develop rapid yet accurate screening assays for the identification of genotoxic liability and for early hazard assessment in drug discovery. The GADD45a-GFP human cell-based genotoxicity assay (GreenScreen HC) has been reformatted to test 12 compounds per 96-well microplate in a higher throughput, automated screening mode and the protocol applied to the analysis of 1266 diverse, pharmacologically active compounds. Testing from a fixed starting concentration of 100 μM and over 3 serial dilutions, the hit rates for genotoxicity (7.3%) and cytotoxicity (33%) endpoints of the assay have been determined in a much wider chemical space than previously reported. The degree of interference from color, autofluorescence, and low solubility has also been assessed. The assay results have been compared to an in silico approach to genotoxicity assessment using Derek for Windows software. Where carcinogenicity data were available, GreenScreen HC demonstrated a higher specificity than in silico methods while identifying genotoxic species that were not highlighted for genotoxic liability in structure-activity relationship software. Higher throughput screening from a fixed, low concentration reduces sensitivity to less potent genotoxins, but the maintenance of the previously reported high specificity is essential in early hazard assessment where misclassification can lead to the needless rejection of potentially useful compounds in drug development. © 2009 Society for Biomolecular Sciences.
机译:迫切需要开发快速而准确的筛选测定法,以鉴定遗传毒性责任并进行药物发现中的早期危害评估。 GADD45a-GFP基于人细胞的遗传毒性测定法(GreenScreen HC)已重新格式化,可以以更高的通量,自动筛选模式在每个96孔微孔板中测试12种化合物,该方案可用于分析1266种多样的药理活性化合物。从100μM的固定起始浓度和3种连续稀释液进行测试,已在比以前报道的更大的化学空间中确定了测定的遗传毒性(7.3%)和细胞毒性(33%)终点的命中率。还评估了颜色,自发荧光和低溶解度的干扰程度。已将分析结果与使用Derek for Windows软件进行计算机遗传毒性评估的计算机方法进行了比较。在有致癌性数据的地方,GreenScreen HC在鉴定结构-活性关系软件中未突出显示遗传毒性责任的遗传毒性物种时,显示出比计算机方法更高的特异性。从固定的低浓度进行更高的通量筛选会降低对弱效基因毒素的敏感性,但是维持早期报道的高特异性对于早期危险评估至关重要,因为早期分类错误会导致不必要的药物开发中可能有用的化合物被拒绝。 ©2009生物分子科学学会。

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