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Sarcoma Cell Line Screen of Oncology Drugs and Investigational Agents Identifies Patterns Associated with Gene and microRNA Expression

机译:肿瘤药物和调查试剂的肉瘤细胞系筛网识别与基因和微稻草表达相关的模式

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摘要

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. (C) 2015 AACR.
机译:Sarcoma表型和基因型的多样性使得这种疾病的治疗特别挑战。筛选六十三种人类成人和儿科肉瘤线,筛选了100种FDA批准的肿瘤学剂和345种研究药物。调查试剂的文献使得具有靶向相同分子实体的几种化合物的比较,允许比较靶特异性和细胞系反应的异质性。基因表达来自外显子阵列数据,并且源自直接数字检测测定的MicroRNA表达。将化合物以九份的九份筛选,含有96小时的三次浓度,使用Alamar Blue作为终点。结果出现了以下靶标的抑制剂:极光激酶,IGF-1R,MEK,BET BROMODOMAIN和PARP1。为选定的实施例介绍了化学结构,IC50热图,浓度响应曲线,基因表达和MIR表达热图。此外,还提出了两种特殊响应者的案例。药物和复合反应,基因表达和MicroRNA表达数据在http://sarcoma.cancer.gov上公开提供。这些数据为癌症研究界提供了独特的资源。 (c)2015年AACR。

著录项

  • 来源
    《Molecular cancer therapeutics》 |2015年第11期|共11页
  • 作者单位

    NCI Dev Therapeut Program Div Canc Treatment &

    Diag Rockville MD USA;

    NCI Biometr Res Branch Div Canc Treatment &

    Diag Rockville MD USA;

    NCI Dev Therapeut Program Div Canc Treatment &

    Diag Rockville MD USA;

    Leidos Biomed Res Inc Mol Pharmacol Grp Frederick Natl Lab Canc Res Frederick MD USA;

    Leidos Biomed Res Inc Mol Pharmacol Grp Frederick Natl Lab Canc Res Frederick MD USA;

    Leidos Biomed Res Inc Mol Pharmacol Grp Frederick Natl Lab Canc Res Frederick MD USA;

    Leidos Biomed Res Inc Mol Pharmacol Grp Frederick Natl Lab Canc Res Frederick MD USA;

    Leidos Biomed Res Inc Mol Pharmacol Grp Frederick Natl Lab Canc Res Frederick MD USA;

    Leidos Biomed Res Inc Mol Pharmacol Grp Frederick Natl Lab Canc Res Frederick MD USA;

    Leidos Biomed Res Inc Mol Pharmacol Grp Frederick Natl Lab Canc Res Frederick MD USA;

    Leidos Biomed Res Inc Mol Pharmacol Grp Frederick Natl Lab Canc Res Frederick MD USA;

    Leidos Biomed Res Inc Mol Pharmacol Grp Frederick Natl Lab Canc Res Frederick MD USA;

    Leidos Biomed Res Inc Mol Pharmacol Grp Frederick Natl Lab Canc Res Frederick MD USA;

    NCI Dev Therapeut Program Div Canc Treatment &

    Diag Rockville MD USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 肿瘤学;
  • 关键词

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