gms | German Medical Science

27. Deutscher Krebskongress

Deutsche Krebsgesellschaft e. V.

22. - 26.03.2006, Berlin

Identification of clinically relevant genes in a functional model of chromosome 8 mediated breast tumor suppression

Meeting Abstract

  • corresponding author presenting/speaker Susanne Seitz - Max Delbrueck Center for Molecular Medicine, Berlin, Deutschland
  • Renate Frege - Max Delbrueck Center for Molecular Medicine, Berlin
  • Anja Jacobsen - University Hospital Schleswig-Holstein, Kiel
  • Jörg Weimer - University Hospital Schleswig-Holstein, Kiel
  • Wolfgang Arnold - atugen AG, Berlin
  • Dieter Niederacher - University of Duesseldorf, Duesseldorf
  • Rita Schmutzler - Gynecology and Obstetrics Clinic, Cologne
  • Norbert Arnold - University Hospital Schleswig-Holstein, Kiel
  • Siegfried Scherneck - Max Delbrueck Center for Molecular Medicine, Berlin

27. Deutscher Krebskongress. Berlin, 22.-26.03.2006. Düsseldorf, Köln: German Medical Science; 2006. DocPO074

Die elektronische Version dieses Artikels ist vollständig und ist verfügbar unter:

Veröffentlicht: 20. März 2006

© 2006 Seitz et al.
Dieser Artikel ist ein Open Access-Artikel und steht unter den Creative Commons Lizenzbedingungen ( Er darf vervielf&aauml;ltigt, verbreitet und &oauml;ffentlich zug&aauml;nglich gemacht werden, vorausgesetzt dass Autor und Quelle genannt werden.



Several lines of evidence suggest that chromosome 8 harbors one or more tumor suppressor genes in breast cancer. We used microcell-mediated transfer of chromosome 8 into MDA-MB-231 breast cancer cells and generated independent hybrids with strongly reduced tumorigenic potential. Loss of the transferred chromosome results in reappearance of the malignant phenotype. Expression profiling using GeneChip DNA microarray analysis identified a set of 109 altered genes (CT8-ps) associated with these phenotypic alterations. We identified CT8-ps networks suggesting that these genes act cooperatively to cause reversion of tumorigenicity in MDA-MB-231 cells. Expression analysis of CT8-ps in a series of human breast tumors revealed several associations with clinicopathological features, including tumor size, grading and age at diagnosis. The combined approach of microcell-mediated chromosome transfer and expression difference analysis provides a conceptual basis and experimental system to identify and evaluate genes and gene networks involved in the development and/or progression of breast cancer. The detailed contextual characterization of the identified CT8-ps will determine the extent of their involvement in breast tumorigenesis.