Table 1

Genes regulated by tyrosine kinase inhibitors

GeneAccession no.Fold change (SD)
imatinib (32D/BCR-ABL)MLN518 (32D/FLT3-ITD)
Genes induced by inhibitors    
    Topoisomerase-inhibitor suppressed D86344 5.5 (0.3) 6.7 (0.8) 
    Mad4 U32395 4.3 (0.3) 3.9 (0.2) 
    Cdk4 and Cdk6 inhibitor p19 U19597 2.0 (0.2) 2.1 (0.6) 
    Eyes absent 2 homolog U81603 2.9 (0.6) 2.9 (0.5) 
    Mnk2 Y11092 2.1 (0.4) 2.4 (0.3) 
    cyclin G2 U95826 10.1(4.6) 6.0 (2.2) 
    Mbd4 AF072249 2.2 (0.1) 1.7 (0.5) 
    Ecotropic viral integration site 2 M34896 3.7 (1.3) 2.8 (0.9) 
    G protein signaling regulator RGS2 U67187 3.3 (1.3) 6.5 (1.9) 
    Hemopoietic cell phosphatase M68902 1.5 (0.2) 2.2 (0.2) 
Genes repressed by inhibitors    
    Cytokine inducible SH2-containing protein D89613 −7.0 (1.0) −4.3 (0.6) 
    Inhibitor of DNA binding1 M31885 −49.0 (6.4) −4.8 (0.9) 
    eIF-1A AF026481 −3.1 (0.6) −3.1 (0.6) 
    Myelocytomatosis oncogene L00039 −11.8 (4.8) −5.5 (0. 9) 
    Bcl2-like L35049 −3.2 (0.6) −2.2 (0.3) 
    SIK similar protein AF053232 −2.6 (0.7) −3.2 (0.6) 
    schlafen2 AF099973 −4.0 (0.5) −2.8 (0.5) 
    cyclin D2 M83749 −7.0 (1.8) −6.9 (1.7) 
    Proviral integration site 1 M13945 −7.8 (3.3) −14.0 (2.9) 
    interleukin-4 receptor (secreted form) M27960 −2.2 (0.2) −4.8 (0.5) 
    proliferation-associated protein 1 U43918 −2.6 (0.3) −2.9 (0.6) 
    protein-serine/threonine kinase (pim-2) L41495 −5.0 (2.0) −7.4 (1.3) 
GeneAccession no.Fold change (SD)
imatinib (32D/BCR-ABL)MLN518 (32D/FLT3-ITD)
Genes induced by inhibitors    
    Topoisomerase-inhibitor suppressed D86344 5.5 (0.3) 6.7 (0.8) 
    Mad4 U32395 4.3 (0.3) 3.9 (0.2) 
    Cdk4 and Cdk6 inhibitor p19 U19597 2.0 (0.2) 2.1 (0.6) 
    Eyes absent 2 homolog U81603 2.9 (0.6) 2.9 (0.5) 
    Mnk2 Y11092 2.1 (0.4) 2.4 (0.3) 
    cyclin G2 U95826 10.1(4.6) 6.0 (2.2) 
    Mbd4 AF072249 2.2 (0.1) 1.7 (0.5) 
    Ecotropic viral integration site 2 M34896 3.7 (1.3) 2.8 (0.9) 
    G protein signaling regulator RGS2 U67187 3.3 (1.3) 6.5 (1.9) 
    Hemopoietic cell phosphatase M68902 1.5 (0.2) 2.2 (0.2) 
Genes repressed by inhibitors    
    Cytokine inducible SH2-containing protein D89613 −7.0 (1.0) −4.3 (0.6) 
    Inhibitor of DNA binding1 M31885 −49.0 (6.4) −4.8 (0.9) 
    eIF-1A AF026481 −3.1 (0.6) −3.1 (0.6) 
    Myelocytomatosis oncogene L00039 −11.8 (4.8) −5.5 (0. 9) 
    Bcl2-like L35049 −3.2 (0.6) −2.2 (0.3) 
    SIK similar protein AF053232 −2.6 (0.7) −3.2 (0.6) 
    schlafen2 AF099973 −4.0 (0.5) −2.8 (0.5) 
    cyclin D2 M83749 −7.0 (1.8) −6.9 (1.7) 
    Proviral integration site 1 M13945 −7.8 (3.3) −14.0 (2.9) 
    interleukin-4 receptor (secreted form) M27960 −2.2 (0.2) −4.8 (0.5) 
    proliferation-associated protein 1 U43918 −2.6 (0.3) −2.9 (0.6) 
    protein-serine/threonine kinase (pim-2) L41495 −5.0 (2.0) −7.4 (1.3) 

Murine 32Dcl3 cells transduced with BCR-ABL or FLT3-ITD were treated with either imatinib or MLN518 for 4 hours. Transcriptional profiles were analyzed using Affymetrix U74 oligonucleotide arrays. Data are from 3 independent experiments. Gene selection criteria: (1) Gene cluster software analysis showed P < .005. (2) Gene is among the top 200 most differentially expressed genes.

“Fold change” indicates the average change in gene expression between samples treated with specific inhibitors and samples treated with nonspecific inhibitors or without any inhibitors; and SD, standard deviation.

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