Analysis of Food and Drug Administration-Approved Anticancer Agents in the NCI60 Panel of Human Tumor Cell Lines

被引:237
作者
Holbeck, Susan L. [1 ]
Collins, Jerry M. [1 ]
Doroshow, James H. [1 ]
机构
[1] NCI, Div Canc Treatment & Diag, Dev Therapeut Program, Informat Technol Branch, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
EXPRESSION; INHIBITORS; SENSITIVITY; DISCOVERY; PATTERNS; UPDATE; GROWTH;
D O I
10.1158/1535-7163.MCT-10-0106
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Since the early 1990s the Developmental Therapeutics Program of the National Cancer Institute (NCI) has utilized a panel of 60 human tumor cell lines (NCI60) representing 9 tissue types to screen for potential new anticancer agents. To date, about 100,000 compounds and 50,000 natural product extracts have been screened. Early in this program it was discovered that the pattern of growth inhibition in these cell lines was similar for compounds of similar mechanism. The development of the COMPARE algorithm provided a means by which investigators, starting with a compound of interest, could identify other compounds whose pattern of growth inhibition was similar. With extensive molecular characterization of these cell lines, COMPARE and other user-defined algorithms have been used to link patterns of molecular expression and drug sensitivity. We describe here the results of screening current Food and Drug Administration (FDA)-approved anticancer agents in the NCI60 screen, with an emphasis on those agents that target signal transduction. We analyzed results from agents with mechanisms of action presumed to be similar; we also carried out a hierarchical clustering of all of these agents. The addition of data from recently approved anticancer agents will increase the utility of the NCI60 databases to the cancer research community. These data are freely accessible to the public on the DTP website (http://dtp.cancer.gov/). The FDA-approved anticancer agents are themselves available from the NCI as a plated set of compounds for research use. Mol Cancer Ther; 9(5); 1451-60. (C) 2010 AACR.
引用
收藏
页码:1451 / 1460
页数:10
相关论文
共 23 条
[1]  
Adams J, 1999, CANCER RES, V59, P2615
[2]   KRAS Mutational Status as a Predictor of Epidermal Growth Factor Receptor Inhibitor Efficacy in Colorectal Cancer [J].
Baynes, Roy D. ;
Gansert, Jennifer .
AMERICAN JOURNAL OF THERAPEUTICS, 2009, 16 (06) :554-561
[3]   MicroRNA expression profiles for the NCI-60 cancer cell panel [J].
Blower, Paul E. ;
Verducci, Joseph S. ;
Lin, Shili ;
Zhou, Jin ;
Chung, Ji-Hyun ;
Dai, Zunyan ;
Liu, Chang-Gong ;
Reinhold, William ;
Lorenzi, Philip L. ;
Kaldjian, Eric P. ;
Croce, Carlo M. ;
Weinstein, John N. ;
Sadee, Wolfgang .
MOLECULAR CANCER THERAPEUTICS, 2007, 6 (05) :1483-1491
[4]  
Cragg GM, 1998, MED RES REV, V18, P315, DOI 10.1002/(SICI)1098-1128(199809)18:5<315::AID-MED3>3.3.CO
[5]  
2-0
[6]   Cytosine methylation profiling of cancer cell lines [J].
Ehrich, Mathias ;
Turner, Julia ;
Gibbs, Peter ;
Lipton, Lara ;
Giovanneti, Mara ;
Cantor, Charles ;
van den Boom, Dirk .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (12) :4844-4849
[7]   Integrative genomic analyses identify MITF as a lineage survival oncogene amplified in malignant melanoma [J].
Garraway, LA ;
Widlund, HR ;
Rubin, MA ;
Getz, G ;
Berger, AJ ;
Ramaswamy, S ;
Beroukhim, R ;
Milner, DA ;
Granter, SR ;
Du, JY ;
Lee, C ;
Wagner, SN ;
Li, C ;
Golub, TR ;
Rimm, DL ;
Meyerson, ML ;
Fisher, DE ;
Sellers, WR .
NATURE, 2005, 436 (7047) :117-122
[8]   Characterization of microRNA expression levels and their biological correlates in human cancer cell lines [J].
Gaur, Arti ;
Jewell, David A. ;
Liang, Yu ;
Ridzon, Dana ;
Moore, Jason H. ;
Chen, Caifu ;
Ambros, Victor R. ;
Israel, Mark A. .
CANCER RESEARCH, 2007, 67 (06) :2456-2468
[9]   Update on NCI in vitro drug screen utilities [J].
Holbeck, SL .
EUROPEAN JOURNAL OF CANCER, 2004, 40 (06) :785-793
[10]  
Holbeck SL, 2004, CANC DRUG DISC DEV, P99