Breast Cancer Research and Treatment

, Volume 104, Issue 1, pp 13–19 | Cite as

MDA-MB-435 cells are derived from M14 Melanoma cells––a loss for breast cancer, but a boon for melanoma research

  • James M. Rae
  • Chad J. Creighton
  • Jeanne M. Meck
  • Bassem R. Haddad
  • Michael D. Johnson
Preclinical Study



The tissue of origin of the cell line MDA-MB-435 has been a matter of debate since analysis of DNA microarray data led Ross et al. (2000, Nat Genet 24(3):227–235) to suggest they might be of melanocyte origin due to their similarity to melanoma cell lines. We have previously shown that MDA-MB-435 cells maintained in multiple laboratories are of common origin to those used by Ross et al. and concluded that MDA-MB-435 cells are not a representative model for breast cancer. We could not determine, however, whether the melanoma-like properties of the MDA-MB-435 cell line are the result of misclassification or due to transdifferention to a melanoma-like phenotype.


We used karyotype, comparative genomic hybridization (CGH), and microsatalite polymorphism analyses, combined with bioinformatics analysis of gene expression and single nucleotide polymorphism (SNP) data, to test the hypothesis that the MDA-MB-435 cell line is derived from the melanoma cell line M14.


We show that the MDA-MB-435 and M14 cell lines are essentially identical with respect to cytogenetic characteristics as well as gene expression patterns and that the minor differences found can be explained by phenotypic and genotypic clonal drift.


All currently available stocks of MDA-MB-435 cells are derived from the M14 melanoma cell line and can no longer be considered a model of breast cancer. These cells are still a valuable system for the study of cancer metastasis and the extensive literature using these cells since 1982 represent a valuable new resource for the melanoma research community.


MDA-MB-435 M14 Breast cancer Melanoma Misidentification 



Comparative Genomic Hybridisation


Single Nucleotide Polymorphism


Short Tandem Repeat


This work was supported in part by the Breast Cancer Research Foundation grant N003173 and and by U-01 GM61373 from the National Institute of General Medical Sciences, Bethesda, MD.


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Copyright information

© Springer Science+Business Media, LLC 2006

Authors and Affiliations

  • James M. Rae
    • 1
  • Chad J. Creighton
    • 2
  • Jeanne M. Meck
    • 3
  • Bassem R. Haddad
    • 4
  • Michael D. Johnson
    • 4
  1. 1.Division of Hematology/Oncology, Department of Internal MedicineUniversity of Michigan Medical CenterAnn ArborUSA
  2. 2.Bioinformatics ProgramUniversity of Michigan Medical CenterAnn ArborUSA
  3. 3.Department of Obstetrics and GynecologyGeorgetown University Medical CenterWashington, DCUSA
  4. 4.Lombardi Cancer Center and Department of OncologyGeorgetown University Medical CenterWashington, DCUSA

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