4.7 Article

Identifying kinase dependency in cancer cells by integrating high-throughput drug screening and kinase inhibition data

Journal

BIOINFORMATICS
Volume 31, Issue 23, Pages 3799-3806

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/btv427

Keywords

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Funding

  1. National Institutes of Health under Ruth L. Kirschstein National Research Service Award [T32CA17468]
  2. National Institutes of Health [P50CA058187, P30CA046934]
  3. Cancer League of Colorado
  4. David F. and Margaret T. Grohne Family Foundation
  5. ARIAD Pharmaceuticals

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Motivation: Targeted kinase inhibitors have dramatically improved cancer treatment, but kinase dependency for an individual patient or cancer cell can be challenging to predict. Kinase dependency does not always correspond with gene expression and mutation status. High-throughput drug screens are powerful tools for determining kinase dependency, but drug polypharmacology can make results difficult to interpret. Results: We developed Kinase Addiction Ranker (KAR), an algorithm that integrates high-throughput drug screening data, comprehensive kinase inhibition data and gene expression profiles to identify kinase dependency in cancer cells. We applied KAR to predict kinase dependency of 21 lung cancer cell lines and 151 leukemia patient samples using published datasets. We experimentally validated KAR predictions of FGFR and MTOR dependence in lung cancer cell line H1581, showing synergistic reduction in proliferation after combining ponatinib and AZD8055.

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