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Cancer Research 69, 5049, June 15, 2009. Published Online First June 2, 2009;
doi: 10.1158/0008-5472.CAN-08-4154
© 2009 American Association for Cancer Research

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Cell, Tumor, and Stem Cell Biology

TOB1 Is Regulated by EGF-Dependent HER2 and EGFR Signaling, Is Highly Phosphorylated, and Indicates Poor Prognosis in Node-Negative Breast Cancer

Mike W. Helms1, Dirk Kemming2, Christopher H. Contag1, Heike Pospisil3, Kai Bartkowiak2, Alice Wang4, Sheng-Yung Chang4, Horst Buerger5 and Burkhard H. Brandt2

1 Departments of Pediatrics, Radiology, and Microbiology and Immunology, Molecular Imaging Program, Stanford University School of Medicine, Stanford, California; 2 UKE Hamburg, Institute for Tumor Biology; 3 University Hamburg, Center for Bioinformatics, Hamburg, Germany; 4 Celera Diagnostics, Alameda, California; and 5 UKM Muenster, Institute for Pathology, Muenster, Germany

Requests for reprints: Burkhard H. Brandt, UKE Hamburg, Martinistr. 52, Hamburg 20246, Germany. Phone: 49-40-42803-7495; Fax: 49-40-42803-5379; E-mail: bu.brandt{at}uke.de.

Key Words: EGF • HER2 • TOB1

Clinical and animal studies have shown that coexpression of the receptor tyrosine kinases HER2 and epidermal growth factor (EGF) receptor (EGFR) indicates a highly metastatic phenotype of breast cancer. In a cellular model of this phenotype using differential gene expression analysis, we identified TOB1 to be up-regulated depending on EGF stimulation and transduction through phosphorylation of HER2 tyrosine 1248. mRNA expression analysis of breast cancers from a cohort of node-negative patients showed significantly shortened distant metastasis-free survival for patients with high TOB1 expression. In subsequent tissue microarray studies of 725 clinical samples, high HER2 and EGF protein levels were significantly correlated with TOB1 expression in breast cancer, whereas EGFR and EGF levels correlated with TOB1 phosphorylation. We did not observe a correlation between TOB1 expression and cyclin D1, which was previously suggested to mediate the antiproliferative effect of unphosphorylated TOB1. A positive correlation of TOB1 phosphorylation status with proliferation marker Ki67 suggests that elevated TOB1 phosphorylation might abrogate the antiproliferative effect of TOB1 in breast cancer. This suggests a new regulatory role for TOB1 in cancer progression with particular significance in HER2- and/or EGFR-positive breast cancers. [Cancer Res 2009;69(12):5049–56]







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
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Copyright © 2009 by the American Association for Cancer Research.