Abstract
Breast cancers that overexpress the ERBB2 tyrosine kinase receptor may be treated with the recombinant humanized monoclonal anti-ERBB2 antibody trastuzumab (herceptin). However, resistance to this targeted therapy is frequent. We have determined the response of 18 breast tumor cell lines to trastuzumab and compared it with the ERBB2 phosphorylation status using antibodies directed against tyrosine residue 1248. We show that sensitivity to trastuzumab is frequently associated with the expression of a phosphorylated ERBB2 protein.
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Acknowledgements
We thank O Segatto for the gift of the MCF7/ERBB2 cell line, S Ethier for the gift of the SUM cell lines and JM Durey for help with the illustrations. This work was supported by Inserm, Institut Paoli-Calmettes, Ligue Nationale Contre le Cancer (Label DB) and Institut National du Cancer (ACI2004-2006, PHRC24-04).
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Ginestier, C., Adélaïde, J., Gonçalvès, A. et al. ERBB2 phosphorylation and trastuzumab sensitivity of breast cancer cell lines. Oncogene 26, 7163–7169 (2007). https://doi.org/10.1038/sj.onc.1210528
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DOI: https://doi.org/10.1038/sj.onc.1210528
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