Anticancer medicines in development: assessment of bioactivity profiles within the National Cancer Institute anticancer screening data

被引:35
作者
Covell, David G. [1 ]
Huang, Ruili
Wallqvist, Anders
机构
[1] NCI, Frederick Dev Therapeut Program, Comp Technol Lab, Screening Technol Branch, Frederick, MD 21702 USA
[2] Sci Applicat Int Corp Frederick Inc, Comp Technol Lab, NCI, Frederick, MD USA
关键词
D O I
10.1158/1535-7163.MCT-06-0787
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We present an analysis of current anticancer compounds that are in phase I, II, or III clinical trials and their structural analogues that have been screened in the National Cancer Institute (NCl) anticancer screening program. Bioactivity profiles, measured across the NCI 60 cell lines, were examined for a correspondence between the type of cancer proposed for clinical testing and selective sensitivity to appropriately matched tumor subpanels in the NCl screen. These results find strongest support for using the NCl anticancer screen to select analogue compounds with selective sensitivity to the leukemia, colon, central nervous system, melanoma, and ovarian panels, but not for renal, prostate, and breast panels. These results are extended to applications of two-dimensional structural features to further refine compound selections based on tumor panel sensitivity obtained from tumor screening results.
引用
收藏
页码:2261 / 2270
页数:10
相关论文
共 38 条
  • [11] Precise nanoliter fluid handling system with integrated high-speed flow sensor
    Haber, C
    Boillat, M
    van der Schoot, B
    [J]. ASSAY AND DRUG DEVELOPMENT TECHNOLOGIES, 2005, 3 (02) : 203 - 212
  • [12] Getting on the critical path: better evaluation tools for drug discovery and development
    Hrusovsky, Kevin
    [J]. DRUG DISCOVERY TODAY, 2006, 11 (17-18) : 773 - 774
  • [13] Linking pathway gene expressions to the growth inhibition response from the National Cancer Institute's anticancer screen and drug mechanism of action
    Huang, R
    Wallqvist, A
    Thanki, N
    Covell, DG
    [J]. PHARMACOGENOMICS JOURNAL, 2005, 5 (06) : 381 - 399
  • [14] Anticancer metal compounds in NCI's tumor-screening database: putative mode of action
    Huang, RL
    Wallqvist, A
    Covell, DG
    [J]. BIOCHEMICAL PHARMACOLOGY, 2005, 69 (07) : 1009 - 1039
  • [15] Correlating gene expression with chemical scaffolds of cytotoxic agents:: ellipticines as substrates and inhibitors of MDR1
    Huang, Y
    Blower, PE
    Yang, C
    Barbacioru, C
    Dai, Z
    Zhang, Y
    Xiao, JJ
    Chan, KK
    Sadée, W
    [J]. PHARMACOGENOMICS JOURNAL, 2005, 5 (02) : 112 - 125
  • [16] Mutation analysis of 24 known cancer genes in the NCI-60 cell line set
    Ikediobi, Ogechi N.
    Davies, Helen
    Bignell, Graham
    Edkins, Sarah
    Stevens, Claire
    O'Meara, Sarah
    Santarius, Thomas
    Avis, Tim
    Barthorpe, Syd
    Brackenbury, Lisa
    Buck, Gemma
    Butler, Adam
    Clements, Jody
    Cole, Jennifer
    Dicks, Ed
    Forbes, Simon
    Gray, Kristian
    Halliday, Kelly
    Harrison, Rachel
    Hills, Katy
    Hinton, Jonathan
    Hunter, Chris
    Jenkinson, Andy
    Jones, David
    Kosmidou, Vivienne
    Lugg, Richard
    Menzies, Andrew
    Mironenko, Tatiana
    Parker, Adrian
    Perry, Janet
    Raine, Keiran
    Richardson, David
    Shepherd, Rebecca
    Small, Alex
    Smith, Raffaella
    Solomon, Helen
    Stephens, Philip
    Teague, Jon
    Tofts, Calli
    Varian, Jennifer
    Webb, Tony
    West, Sofie
    Widaa, Sara
    Yates, Andy
    Reinhold, William
    Weinstein, John N.
    Stratton, Michael R.
    Futreal, P. Andrew
    Wooster, Richard
    [J]. MOLECULAR CANCER THERAPEUTICS, 2006, 5 (11) : 2606 - 2612
  • [17] Key aspects of the novartis compound collection enhancement project for the compilation of a comprehensive chemogenomics drug discovery screening collection
    Jacoby, E
    Schuffenhauer, A
    Popov, M
    Azzaoui, K
    Havill, B
    Schopfer, U
    Engeloch, C
    Stanek, J
    Acklin, P
    Rigollier, P
    Stoll, F
    Koch, G
    Meier, P
    Orain, D
    Giger, R
    Hinrichs, J
    Malagu, K
    Zimmermann, J
    Roth, HJ
    [J]. CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2005, 5 (04) : 397 - 411
  • [18] Protein-linked DNA strand breaks induced by NSC 314622, a novel noncamptothecin topoisomerase I poison
    Kohlhagen, G
    Paull, KD
    Cushman, M
    Nagafuji, P
    Pommier, Y
    [J]. MOLECULAR PHARMACOLOGY, 1998, 54 (01) : 50 - 58
  • [19] Lam LT, 2005, CLIN CANCER RES, V11, P28
  • [20] The use of receiver operating characteristic curves in biomedical informatics
    Lasko, TA
    Bhagwat, JG
    Zou, KH
    Ohno-Machado, L
    [J]. JOURNAL OF BIOMEDICAL INFORMATICS, 2005, 38 (05) : 404 - 415