Literature DB >> 8023045

Discrimination techniques applied to the NCI in vitro anti-tumour drug screen: predicting biochemical mechanism of action.

A D Koutsoukos1, L V Rubinstein, D Faraggi, R M Simon, S Kalyandrug, J N Weinstein, K W Kohn, K D Paull.   

Abstract

The National Cancer Institute currently tests approximately 400 compounds per week against a panel of human tumour cell lines in order to identify potential anti-cancer drugs. We describe several approaches, based on these in vitro data, to the problem of identifying the primary biochemical mechanism of action of a compound. Using linear and non-parametric discriminant procedures and cross-validation, we find that accurate identification of the mechanism of action is achieved for approximately 90 per cent of a diverse collection of 141 known compounds, representing six different mechanistic categories. We demonstrate that two-dimensional graphical displays of the compounds in terms of the initial three principal components (of the original data) result in suggestive visual clustering according to mechanism of action. Finally, we compare the classification accuracy of the statistical discrimination procedures with the accuracy obtained from a neural network approach and, for our example, we find that the results obtained from the various approaches are similar.

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Year:  1994        PMID: 8023045     DOI: 10.1002/sim.4780130532

Source DB:  PubMed          Journal:  Stat Med        ISSN: 0277-6715            Impact factor:   2.373


  8 in total

1.  A multivariate insight into the in vitro antitumour screen database of the National Cancer Institute: classification of compounds, similarities among cell lines and the influence of molecular targets.

Authors:  G Musumarra; D F Condorelli; A S Costa; M Fichera
Journal:  J Comput Aided Mol Des       Date:  2001-03       Impact factor: 3.686

2.  Classification of a large anticancer data set by adaptive fuzzy partition.

Authors:  Nadège Piclin; Marco Pintore; Christophe Wechman; Jacques R Chrétien
Journal:  J Comput Aided Mol Des       Date:  2004 Jul-Sep       Impact factor: 3.686

Review 3.  A cheminformatic toolkit for mining biomedical knowledge.

Authors:  Gus R Rosania; Gordon Crippen; Peter Woolf; David States; Kerby Shedden
Journal:  Pharm Res       Date:  2007-03-24       Impact factor: 4.200

Review 4.  Flow cytometry and cell sorting of heterogeneous microbial populations: the importance of single-cell analyses.

Authors:  H M Davey; D B Kell
Journal:  Microbiol Rev       Date:  1996-12

Review 5.  Molecular targets in the National Cancer Institute drug screen.

Authors:  S E Bates; A T Fojo; J N Weinstein; T G Myers; M Alvarez; K D Pauli; B A Chabner
Journal:  J Cancer Res Clin Oncol       Date:  1995       Impact factor: 4.553

6.  A strategy for primary high throughput cytotoxicity screening in pharmaceutical toxicology.

Authors:  P J Bugelski; U Atif; S Molton; I Toeg; P G Lord; D G Morgan
Journal:  Pharm Res       Date:  2000-10       Impact factor: 4.200

7.  Epidermal growth factor receptor-targeted therapy potentiates lovastatin-induced apoptosis in head and neck squamous cell carcinoma cells.

Authors:  Angela J Mantha; Kathryn E McFee; Nima Niknejad; Glenwood Goss; Ian A Lorimer; Jim Dimitroulakos
Journal:  J Cancer Res Clin Oncol       Date:  2003-08-26       Impact factor: 4.553

8.  In vitro cross-resistance and collateral sensitivity in seven resistant small-cell lung cancer cell lines: preclinical identification of suitable drug partners to taxotere, taxol, topotecan and gemcitabin.

Authors:  P B Jensen; B Holm; M Sorensen; I J Christensen; M Sehested
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

  8 in total

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