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

被引:65
作者
Rae, JM
Ramus, SJ
Waltham, M
Armes, JE
Campbell, IG
Clarke, R
Barndt, RJ
Johnson, MD
Thompson, EW
机构
[1] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[2] Univ Melbourne, Dept Pathol, Victorian Breast Canc Res Consortium Grp Mol Path, Parkville, Vic 3052, Australia
[3] St Vincents Inst Med Res, Victorian Breast Canc Res Consortium Grp Invas &, Melbourne, Vic, Australia
[4] Peter MacCallum Canc Ctr, Victorian Breast Canc Res Consortium Grp Breast C, Melbourne, Vic, Australia
[5] Univ Melbourne, Dept Pathol, Melbourne, Vic, Australia
[6] Univ Melbourne, Dept Surg, Melbourne, Vic, Australia
[7] Univ Melbourne, Dept Obstet & Gynaecol, Melbourne, Vic, Australia
[8] Bernard OBrien Inst Microsurg, Melbourne, Vic, Australia
[9] Georgetown Univ, Med Ctr, Lombardi Comprehens Canc Ctr, Washington, DC 20007 USA
[10] Georgetown Univ, Med Ctr, Dept Oncol, Washington, DC 20007 USA
关键词
MDA-MB-435; breast cancer; cell lines; melanoma; microsatellite analysis; chromosomal number; tyrosinase;
D O I
10.1007/s10585-004-3759-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:543 / 552
页数:10
相关论文
共 31 条
[1]   Epidermal growth factor-induced epithelio-mesenchymal transition in human breast carcinoma cells [J].
Ackland, ML ;
Newgreen, DF ;
Fridman, M ;
Waltham, MC ;
Arvanitis, A ;
Minichiello, J ;
Price, JT ;
Thompson, EW .
LABORATORY INVESTIGATION, 2003, 83 (03) :435-448
[2]  
Bahia H, 2002, INT J ONCOL, V20, P489
[3]  
CAILLEAU R, 1978, IN VITRO CELL DEV B, V14, P911
[4]  
CLARKE R, 2000, DIS BREAST, P319
[5]  
CLARKE R, 1995, DIS BREAST
[6]   Molecular cytogenetic analysis of breast cancer cell lines [J].
Davidson, JM ;
Gorringe, KL ;
Chin, SF ;
Orsetti, B ;
Besret, C ;
Courtay-Cahen, C ;
Roberts, I ;
Theillet, C ;
Caldas, C ;
Edwards, PAW .
BRITISH JOURNAL OF CANCER, 2000, 83 (10) :1309-1317
[7]   Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868
[8]   Further evidence to support the melanocytic origin of MDA-MB-435 [J].
Ellison, G ;
Klinowska, T ;
Westwood, RFR ;
Docter, E ;
French, T ;
Fox, JC .
JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY, 2002, 55 (05) :294-299
[9]  
GILLES C, 1996, BREAST J, V2, P83
[10]   Molecular biology of breast cancer metastasis - Molecular expression of vascular markers by aggressive breast cancer cells [J].
Hendrix, MJC ;
Seftor, EA ;
Kirschmann, DA ;
Seftor, REB .
BREAST CANCER RESEARCH, 2000, 2 (06) :417-422