Home LiteratureArticle Details
PMID: 20964822 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Mapping the cellular and molecular heterogeneity of normal and malignant breast tissues and cultured cell lines.

Breast cancer research : BCR ·Vol. 12 ·No. 5 ·2010-00-00 ·Pages R87

Keller PJ, Lin AF, Arendt LM, Klebba I, Jones AD, Rudnick JA, DiMeo TA, Gilmore H, Jefferson DM, Graham RA, Naber SP, Schnitt S, Kuperwasser C

Abstract

Normal and neoplastic breast tissues are comprised of heterogeneous populations of epithelial cells involving various degrees of maturation and differentiation. While cultured cell lines have been derived from both normal and malignant tissues, it remains unclear whether they retain a similar cellular heterogeneity as to that found within breast tissues. We used 12 reduction mammoplasty tissues, 15 primary breast cancer tissues, and 20 human breast epithelial cell lines (16 cancer lines, 4 normal lines) to perform flow cytometry for CD44, CD24, epithelial cell adhesion molecule (EpCAM), and CD49f expression as well as immunohistochemistry, and in vivo tumor xenograft formation studies to extensively analyze the molecular and cellular characteristics of breast epithelial cell lineages. Human breast tissues contain four distinguishable epithelial differentiation states (two luminal phenotypes and two basal phenotypes) that differ on the basis of CD24, EpCAM and CD49f expression. Primary human breast cancer tissues also contain these four cellular states, but in altered proportions compared to normal tissues. In contrast, cultured cancer cell lines are enriched for rare basal and mesenchymal phenotypes, which are normally present in small numbers within human tissues. Similarly, cultured normal human mammary epithelial cell lines were enriched for rare basal and mesenchymal phenotypes that represent a minor fraction of cells within reduction mammoplasty tissues. Although normal human mammary epithelial cell lines exhibited features of bi-potent progenitor cells they were unable to differentiate into mature luminal breast epithelial cells. As a group breast cancer cell lines represent the heterogeneity of human breast tumors, but individually they exhibit increased lineage-restricted profiles that fall short of truly representing the intratumoral heterogeneity of individual breast tumors. Additionally, normal human mammary epithelial cell lines fail to retain much of the cellular diversity found in human breast tissues and are enriched for differentiation states that are a minority in breast tissues, although they do exhibit features of bi-potent basal progenitor cells. These findings suggest that collections of cell lines representing multiple cell types can be used to model the cellular heterogeneity of tissues.

MeSH Terms
Animals Antigens, Neoplasm/analysis Biomarkers, Tumor/analysis,genetics Breast/cytology,pathology Breast Neoplasms/genetics,pathology CD24 Antigen/analysis Cell Adhesion Molecules/analysis Cell Differentiation Cell Line, Tumor Epithelial Cell Adhesion Molecule Epithelial Cells/cytology,pathology Female Gene Expression Humans Hyaluronan Receptors/analysis Integrin alpha6/analysis Mice Mice, Inbred NOD Mice, SCID
Chemicals
Antigens, Neoplasm Biomarkers, Tumor CD24 Antigen Cell Adhesion Molecules EPCAM protein, human Epithelial Cell Adhesion Molecule Hyaluronan Receptors Integrin alpha6
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
Keller Patrica J
Department of Anatomy & Cellular Biology, Sackler School, Tufts University School of Medicine, Boston, MA 02111, USA.
Lin Amy F
Arendt Lisa M
Klebba Ina
Jones Ainsely D
Rudnick Jenny A
DiMeo Theresa A
Gilmore Hannah
Jefferson Douglas M
Graham Roger A
Naber Stephen P
Schnitt Stuart
Kuperwasser Charlotte
References (37)
37 references, click to expand
  1. Human breast cancer cells generated by oncogenic transformation of primary mammary epithelial cells.
    Genes Dev. 2001 Jan 1;15(1):50-65 PMID: 11156605
  2. Evidence for a stem cell hierarchy in the adult human breast.
    J Cell Biol. 2007 Apr 9;177(1):87-101 PMID: 17420292
  3. Relevance of breast cancer cell lines as models for breast tumours: an update.
    Breast Cancer Res Treat. 2004 Feb;83(3):249-89 PMID: 14758095
  4. A method for quantifying normal human mammary epithelial stem cells with in vivo regenerative ability.
    Nat Med. 2008 Dec;14(12):1384-9 PMID: 19029987
  5. Repeated observation of breast tumor subtypes in independent gene expression data sets.
    Proc Natl Acad Sci U S A. 2003 Jul 8;100(14):8418-23 PMID: 12829800
  6. Gene expression profiling predicts clinical outcome of breast cancer.
    Nature. 2002 Jan 31;415(6871):530-6 PMID: 11823860
  7. Characterization of bipotent mammary epithelial progenitor cells in normal adult human breast tissue.
    Breast Cancer Res Treat. 2001 May;67(2):93-109 PMID: 11519870
  8. Distinct gene mutation profiles among luminal-type and basal-type breast cancer cell lines.
    Breast Cancer Res Treat. 2010 May;121(1):53-64 PMID: 19593635
  9. Cell aging in vivo and in vitro.
    Mech Ageing Dev. 1997 Oct;98(1):1-35 PMID: 9255755
  10. Gene expression patterns of breast carcinomas distinguish tumor subclasses with clinical implications.
    Proc Natl Acad Sci U S A. 2001 Sep 11;98(19):10869-74 PMID: 11553815
  11. Human breast cancer cell lines contain stem-like cells that self-renew, give rise to phenotypically diverse progeny and survive chemotherapy.
    Breast Cancer Res. 2008;10(2):R25 PMID: 18366788
  12. A collection of breast cancer cell lines for the study of functionally distinct cancer subtypes.
    Cancer Cell. 2006 Dec;10(6):515-27 PMID: 17157791
  13. Prediction of drug resistance in cancer chemotherapy: the Kern and DiSC assays.
    Oncology (Williston Park). 1991 Sep;5(9):93-103; disc. 104, 111-4, 117-8 PMID: 1835882
  14. Gata-3 is an essential regulator of mammary-gland morphogenesis and luminal-cell differentiation.
    Nat Cell Biol. 2007 Feb;9(2):201-9 PMID: 17187062
  15. Evidence for in vitro selection during cell culturing of breast cancer: detection by flow and image cytometry.
    Cancer Genet Cytogenet. 1999 Oct 15;114(2):154-5 PMID: 10549274
  16. CD44+/CD24- breast cancer cells exhibit enhanced invasive properties: an early step necessary for metastasis.
    Breast Cancer Res. 2006;8(5):R59 PMID: 17062128
  17. Reconstruction of human mammary tissues in a mouse model.
    Nat Protoc. 2006;1(1):206-14 PMID: 17406234
  18. Heterogeneity for stem cell-related markers according to tumor subtype and histologic stage in breast cancer.
    Clin Cancer Res. 2010 Feb 1;16(3):876-87 PMID: 20103682
  19. Molecular portraits of human breast tumours.
    Nature. 2000 Aug 17;406(6797):747-52 PMID: 10963602
  20. Two types of normal human breast epithelial cells derived from reduction mammoplasty: phenotypic characterization and response to SV40 transfection.
    Carcinogenesis. 1995 Mar;16(3):531-8 PMID: 7697810
  21. Gene expression profiling of breast cell lines identifies potential new basal markers.
    Oncogene. 2006 Apr 6;25(15):2273-84 PMID: 16288205
  22. Comparison of features of human breast cancer cell lines and their corresponding tumors.
    Clin Cancer Res. 1998 Dec;4(12):2931-8 PMID: 9865903
  23. Molecular definition of breast tumor heterogeneity.
    Cancer Cell. 2007 Mar;11(3):259-73 PMID: 17349583
  24. Immunohistochemical and clinical characterization of the basal-like subtype of invasive breast carcinoma.
    Clin Cancer Res. 2004 Aug 15;10(16):5367-74 PMID: 15328174
  25. Transcriptome analysis of the normal human mammary cell commitment and differentiation process.
    Cell Stem Cell. 2008 Jul 3;3(1):109-18 PMID: 18593563
  26. Aberrant luminal progenitors as the candidate target population for basal tumor development in BRCA1 mutation carriers.
    Nat Med. 2009 Aug;15(8):907-13 PMID: 19648928
  27. Isolation and characterization of a spontaneously immortalized human breast epithelial cell line, MCF-10.
    Cancer Res. 1990 Sep 15;50(18):6075-86 PMID: 1975513
  28. Cancer cell lines as genetic models of their parent histology: analyses based on array comparative genomic hybridization.
    Cancer Res. 2007 Apr 15;67(8):3594-600 PMID: 17440070
  29. Molecular profiling of breast cancer cell lines defines relevant tumor models and provides a resource for cancer gene discovery.
    PLoS One. 2009 Jul 03;4(7):e6146 PMID: 19582160
  30. Expression of basal and luminal epithelium-specific keratins in normal, benign, and malignant breast tissue.
    J Natl Cancer Inst. 1988 Jul 6;80(9):691-5 PMID: 2453676
  31. Cyclin D1 kinase activity is required for the self-renewal of mammary stem and progenitor cells that are targets of MMTV-ErbB2 tumorigenesis.
    Cancer Cell. 2010 Jan 19;17(1):65-76 PMID: 20129248
  32. Transformation of different human breast epithelial cell types leads to distinct tumor phenotypes.
    Cancer Cell. 2007 Aug;12(2):160-70 PMID: 17692807
  33. Methylation of p16(INK4a) promoters occurs in vivo in histologically normal human mammary epithelia.
    Cancer Res. 2003 Apr 1;63(7):1596-601 PMID: 12670910
  34. In vitro propagation and transcriptional profiling of human mammary stem/progenitor cells.
    Genes Dev. 2003 May 15;17(10):1253-70 PMID: 12756227
  35. Re-evaluation of mammary stem cell biology based on in vivo transplantation.
    Breast Cancer Res. 2008;10(1):203 PMID: 18304381
  36. Discovering moderate-risk breast cancer susceptibility genes.
    Curr Opin Genet Dev. 2010 Jun;20(3):268-76 PMID: 20346647
  37. Gene expression profiles of primary breast tumors maintained in distant metastases.
    Proc Natl Acad Sci U S A. 2003 Dec 23;100(26):15901-5 PMID: 14665696
Article Info
Journal
Breast cancer research : BCR
Abbr.
Breast Cancer Res
ISSN
1465-542X
Published
2010-00-00
Epub
2010-00-21
Pages
R87
Language
English
Region
England
NLM ID
100927353
PMCID
PMC3096980
Subset
IM
Grants
NCRR NIH HHS · K01-RR021858 · United States
NCI NIH HHS · R01CA125554 · United States
Corrections
CommentIn
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]