Teicher Beverly A, Polley Eric, Kunkel Mark, Evans David, Silvers Thomas, Delosh Rene, Laudeman Julie, Ogle Chad, Reinhart Russell, Selby Michael, Connelly John, Harris Erik, Monks Anne, Morris Joel
Developmental Therapeutics Program, Division of Cancer Treatment and Diagnosis, National Cancer Institute, Rockville, Maryland.
Biometric Research Branch, Division of Cancer Treatment and Diagnosis, National Cancer Institute, Rockville, Maryland.
Mol Cancer Ther. 2015 Nov;14(11):2452-62. doi: 10.1158/1535-7163.MCT-15-0074. Epub 2015 Sep 8.
The diversity in sarcoma phenotype and genotype make treatment of this family of diseases exceptionally challenging. Sixty-three human adult and pediatric sarcoma lines were screened with 100 FDA-approved oncology agents and 345 investigational agents. The investigational agents' library enabled comparison of several compounds targeting the same molecular entity allowing comparison of target specificity and heterogeneity of cell line response. Gene expression was derived from exon array data and microRNA expression was derived from direct digital detection assays. The compounds were screened against each cell line at nine concentrations in triplicate with an exposure time of 96 hours using Alamar blue as the endpoint. Results are presented for inhibitors of the following targets: aurora kinase, IGF-1R, MEK, BET bromodomain, and PARP1. Chemical structures, IC50 heat maps, concentration response curves, gene expression, and miR expression heat maps are presented for selected examples. In addition, two cases of exceptional responders are presented. The drug and compound response, gene expression, and microRNA expression data are publicly available at http://sarcoma.cancer.gov. These data provide a unique resource to the cancer research community.
肉瘤表型和基因型的多样性使得这类疾病的治疗极具挑战性。用100种美国食品药品监督管理局(FDA)批准的肿瘤药物和345种研究性药物对63种成人和儿童肉瘤细胞系进行了筛选。研究性药物库使得能够比较几种针对同一分子实体的化合物,从而比较细胞系反应的靶点特异性和异质性。基因表达来自外显子阵列数据,微小RNA表达来自直接数字检测分析。使用阿拉玛蓝作为终点指标,将化合物以九种浓度一式三份地针对每个细胞系进行筛选,暴露时间为96小时。给出了以下靶点抑制剂的结果:极光激酶、胰岛素样生长因子-1受体(IGF-1R)、丝裂原活化蛋白激酶/细胞外信号调节激酶(MEK)、含溴结构域蛋白(BET)溴结构域和聚(ADP-核糖)聚合酶1(PARP1)。给出了所选实例的化学结构、半数抑制浓度(IC50)热图、浓度反应曲线、基因表达和微小RNA表达热图。此外,还介绍了两例特别敏感的病例。药物和化合物反应、基因表达以及微小RNA表达数据可在http://sarcoma.cancer.gov上公开获取。这些数据为癌症研究界提供了一个独特的资源。