TY - JOUR
T1 - Sarcoma cell line screen of oncology drugs and investigational agents identifies patterns associated with gene and microRNA expression
AU - Teicher, Beverly A.
AU - Polley, Eric
AU - Kunkel, Mark
AU - Evans, David
AU - Silvers, Thomas
AU - Delosh, Rene
AU - Laudeman, Julie
AU - Ogle, Chad
AU - Reinhart, Russell
AU - Selby, Michael
AU - Connelly, John
AU - Harris, Erik
AU - Monks, Anne
AU - Morris, Joel
N1 - Funding Information:
This project has been funded in whole or in part with federal funds from the National Cancer Institute, NIH, under contract no. HHSN261200800001E. This research was supported (in part) by the Developmental Therapeutics Program in the Division of Cancer Treatment and Diagnosis of the National Cancer Institute.
Publisher Copyright:
© 2015 American Association for Cancer Research.
PY - 2015/11/1
Y1 - 2015/11/1
N2 - 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, andmiR 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.
AB - 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, andmiR 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.
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U2 - 10.1158/1535-7163.MCT-15-0074
DO - 10.1158/1535-7163.MCT-15-0074
M3 - Article
C2 - 26351324
AN - SCOPUS:84958212060
SN - 1535-7163
VL - 14
SP - 2452
EP - 2462
JO - Molecular cancer therapeutics
JF - Molecular cancer therapeutics
IS - 11
ER -