ERBB2 phosphorylation and trastuzumab sensitivity of breast cancer cell lines

被引:57
作者
Ginestier, C.
Adelaiede, J.
Goncalves, A.
Repellini, L.
Sircoulomb, F.
Letessier, A.
Finetti, P.
Geneix, J.
Charafe-Jauffret, E.
Bertucci, F.
Jacquemier, J.
Viens, P.
Birnbaum, D.
机构
[1] Inst J Paoli I Calmettes, Ctr Rech Cancerol Marseille, INSERM, UMR599,Dept Oncol Mol, F-13009 Marseille, France
[2] Inst J Paoli I Calmettes, Ctr Rech Cancerol Marseille, INSERM, UMR599,Dept Oncol Med, F-13009 Marseille, France
[3] Univ Mediterranee, Fac Med, Marseille, France
[4] Inst J Paoli I Calmettes, Dept BioPathol, F-13009 Marseille, France
关键词
herceptin; trastuzumab; ERBB2; breast cancer; phosphorylation; tyrosine kinase;
D O I
10.1038/sj.onc.1210528
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
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.
引用
收藏
页码:7163 / 7169
页数:7
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