Abstract
Recently, the tissue origin of MDA-MB-435 cell line has been the subject of considerable debate. In this study, we set out to determine whether MDA-MB-435-DTP cells shown to express melanoma-specific genes were identical to various other MDA-MB-435 cell stocks worldwide. CGH-microarray, genetic polymorphism genotyping, microsatellite fingerprint analysis and/or chromosomal number confirmed that the MDA-MB-435 cells maintained at the Lombardi Comprehensive Cancer Center (MDA-MB-435-LCC) are almost identical to the MDA-MB-435-DTP cells, and showed a very similar profile to those obtained from the same original source (MD Anderson Cancer Center) but maintained independently (MDA-MB-435-PMCC). Gene expression profile analysis confirmed common expression of genes among different MDA-MB-435-LCC cell stocks, and identified some unique gene products in MDA-MB-435-PMCC cells. RT-PCR analysis confirmed the expression of the melanoma marker tyrosinase across multiple MDA-MB-435 cell stocks. Collectively, our results show that the MDA-MB-435 cells used widely have identical origins to those that exhibit a melanoma-like gene expression signature, but exhibit a small degree of genotypic and phenotypic drift.
MeSH Terms
Biomarkers, Tumor/metabolism
Breast Neoplasms/genetics,metabolism,pathology
DNA, Neoplasm/genetics
Female
Gene Expression
Humans
Melanocytes/pathology
Melanoma/genetics,metabolism,pathology
Microsatellite Repeats
Neoplasm Proteins/metabolism
Nucleic Acid Hybridization
Ploidies
Reverse Transcriptase Polymerase Chain Reaction
Skin Neoplasms/genetics,metabolism,pathology
Tumor Cells, Cultured/classification,metabolism,pathology
Chemicals
Biomarkers, Tumor
DNA, Neoplasm
Neoplasm Proteins
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Rae James M
Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Ramus Susan J
Waltham Mark
Armes Jane E
Campbell Ian G
Clarke Robert
Barndt Robert J
Johnson Michael D
Thompson Erik W
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