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A reason why the ERBB2 gene is amplified and not mutated in breast cancer

Daniel Birnbaum1 email, Fabrice Sircoulomb1,2 email and Jean Imbert2,3 email

Centre de Recherche en Cancérologie de Marseille, UMR891 Inserm and Institut Paoli-Calmettes, Marseille, F-13009, France

Université de la Méditerranée, Marseille, Cedex 09, F-13288, France

U928 Inserm, TAGC, Marseille-Luminy, France

author email corresponding author email

Cancer Cell International 2009, 9:5doi:10.1186/1475-2867-9-5

Published: 18 February 2009

Abstract

Alterations of receptor-type tyrosine kinases (RTK) are frequent in human cancers. They can result from translocation, mutation or amplification. The ERBB2 RTK is encoded by a gene that is amplified in about 20% breast cancers. The question is: why is this RTK specifically subjected to this type of alteration? We propose that ERBB2 gene amplification is used to overcome repression of its expression by sequence-specific transcription factors.


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