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PMID: 15679052 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Common origins of MDA-MB-435 cells from various sources with those shown to have melanoma properties.

Clinical & experimental metastasis ·Vol. 21 ·No. 6 ·2004-00-00 ·Pages 543-52

Rae JM, Ramus SJ, Waltham M, Armes JE, Campbell IG, Clarke R, Barndt RJ, Johnson MD, Thompson EW

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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Article Info
Journal
Clinical & experimental metastasis
Abbr.
Clin Exp Metastasis
ISSN
0262-0898
Published
2004-00-00
Pages
543-52
Language
English
Region
Netherlands
NLM ID
8409970
Subset
IM
Grants
NCI NIH HHS · R21 CA 87244-01 · United States
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