Characterization of a novel, trastuzumab resistant human breast cancer cell line

Mark Barok, Margit Balazs, Viktoria Lazar, Zsuzsa Rakosy, Eniko Toth, Andrea Treszl, Gyorgy Vereb, Gail T. Colbern, John W. Park, Janos Szollosi

Research output: Contribution to journalArticle

2 Citations (Scopus)


HER2-positive breast cancers represent a distinct phenotype and are intrinsically more aggressive than HER2-negative tumors. Although HER2-targeted therapies have been rationally developed, resistance to these treatments represents a process understood poorly. There are few experimental models that allow studying the molecular mechanism of resistance. Our aim was to characterize a trastuzumab resistant breast cancer cell line (B585) that was established from an invasive ductal carcinoma. B585 grows only in immunodeficient mice as a xenograft. CGH and FISH were used to define cytogenetic alterations, gene-expression analysis and immunohistochemistry were applied to detect RNA and protein expression. By array-CGH focused amplifications were identified for C-MYC, EGFR, ErbB2, CCND1 and TOP2-A oncogenes. ErbB2 was co-amplified with TOP2-A. mRNA overexpression was detected for the amplified genes. ErbB2 protein was overexpressed and showed heterogeneous distribution. In summary, molecular cytogenetic analysis and expression profiling of B585 revealed several new alterations. Based on the experiments performed in SCID mice and the genotypic/phenotypic characteristics, this new in vivo breast cancer xenograft is a valuable model to investigate molecular mechanism of trastuzumab resistance.

Original languageEnglish
Pages (from-to)627-640
Number of pages14
JournalFrontiers in Bioscience - Elite
Volume2 E
Issue number2
Publication statusPublished - Jan 1 2010


  • Array-CGH
  • Breast tumor xenograft
  • Drug resistance
  • ErbB2/HER-2
  • Gene and protein expression
  • Trastuzumab

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Immunology and Microbiology(all)

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