Giubellino Alessio, Shankavaram Uma, Bullova Petra, Schovanek Jan, Zhang Yaqin, Shen Min, Patel Nikita, Elkahloun Abdel, Lee Min-Jung, Trepel Jane, Ferrer Marc, Pacak Karel
Program in Reproductive and Adult Endocrinology, Eunice Kennedy Shriver National Institute of Child Health & Human Development, NIH, Bethesda, Maryland, United States of America.
Radiation Oncology Branch, National Cancer Institute, NIH, Bethesda, Maryland, United States of America.
PLoS One. 2014 Apr 3;9(4):e90458. doi: 10.1371/journal.pone.0090458. eCollection 2014.
Drug repurposing or repositioning is an important part of drug discovery that has been growing in the last few years for the development of therapeutic options in oncology. We applied this paradigm in a screening of a library of about 3,800 compounds (including FDA-approved drugs and pharmacologically active compounds) employing a model of metastatic pheochromocytoma, the most common tumor of the adrenal medulla in children and adults. The collection of approved drugs was screened in quantitative mode, testing the compounds in compound-titration series (dose-response curves). Analysis of the dose-response screening data facilitated the selection of 50 molecules with potential bioactivity in pheochromocytoma cells. These drugs were classified based on molecular/cellular targets and signaling pathways affected, and selected drugs were further validated in a proliferation assay and by flow cytometric cell death analysis. Using meta-analysis information from molecular targets of the top drugs identified by our screening with gene expression data from human and murine microarrays, we identified potential drugs to be used as single drugs or in combination. An example of a combination with a synergistic effect is presented. Our study exemplifies a promising model to identify potential drugs from a group of clinically approved compounds that can more rapidly be implemented into clinical trials in patients with metastatic pheochromocytoma or paraganglioma.
药物重新利用或重新定位是药物研发的重要组成部分,在过去几年中,它在肿瘤学治疗方案的开发中不断发展。我们将这种模式应用于对一个约3800种化合物(包括FDA批准的药物和药理活性化合物)库的筛选,采用转移性嗜铬细胞瘤模型,这是儿童和成人肾上腺髓质最常见的肿瘤。对已批准药物的收集进行了定量筛选,在化合物滴定系列(剂量反应曲线)中测试这些化合物。对剂量反应筛选数据的分析有助于选择50种在嗜铬细胞瘤细胞中具有潜在生物活性的分子。这些药物根据受影响的分子/细胞靶点和信号通路进行分类,所选药物在增殖试验和流式细胞术细胞死亡分析中进一步得到验证。利用我们筛选出的顶级药物的分子靶点的荟萃分析信息以及来自人和小鼠微阵列的基因表达数据,我们确定了可单独使用或联合使用的潜在药物。给出了一个具有协同效应的联合用药示例。我们的研究例证了一个有前景的模型,可从一组临床批准的化合物中识别潜在药物,这些药物可更快地应用于转移性嗜铬细胞瘤或副神经节瘤患者的临床试验。