首页> 美国卫生研究院文献>other >Sarcoma Cell Line Screen of Oncology Drugs and Investigational Agents Identifies Patterns Associated with Gene and microRNA Expression
【2h】

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

机译:肿瘤药物和研究药物的肉瘤细胞系筛查可确定与基因和microRNA表达相关的模式

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

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 9 concentrations in triplicate with an exposure time of 96 hrs 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 . These data provide a unique resource to the cancer research community.
机译:肉瘤表型和基因型的多样性使该家族疾病的治疗异常困难。用100种FDA批准的肿瘤药物和345种研究药物筛选了63个人类成年和儿科肉瘤细胞系。研究试剂库能够比较几种靶向同一分子实体的化合物,从而可以比较靶标特异性和细胞系反应的异质性。基因表达源自外显子阵列数据,microRNA表达源自直接数字检测分析。使用Alamar蓝作为终点,针对每种细胞系以9种浓度一式三份筛选化合物,暴露时间为96小时。给出了以下靶标抑制剂的结果:极光激酶,IGF-1R,MEK,BET溴结构域和PARP1。给出了所选实例的化学结构,IC50热图,浓度响应曲线,基因表达和miR表达热图。此外,还介绍了两个例外响应者的案例。药物和化合物反应,基因表达和microRNA表达数据可在上公开获得。这些数据为癌症研究界提供了独特的资源。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号