Literature DB >> 14521514

Epithelial progenitor cell lines as models of normal breast morphogenesis and neoplasia.

Ole William Petersen1, Thorarinn Gudjonsson, René Villadsen, Mina J Bissell, Lone Rønnov-Jessen.   

Abstract

The majority of human breast carcinomas exhibit luminal characteristics and as such, are most probably derived from progenitor cells within the luminal epithelial compartment. This has been subdivided recently into at least three luminal subtypes based on gene expression patterns. The value of knowing the cellular origin of individual tumours is clear and should aid in designing effective therapies. To do this, however, we need strategies aimed at defining the nature of stem and progenitor cell populations in the normal breast. In this review, we will discuss our technical approach for delineating the origin of the epithelial cell types. A major step forward was the purification of each cell type by the application of immunomagnetic cell sorting based on expression of lineage-specific surface antigens. We then developed chemically defined media that could support either the luminal epithelial or the myoepithelial cell phenotype in primary cultures. Having succeeded in continuous propagation presumably without loss of markers, we could show that a subset of the luminal epithelial cells could convert to myoepithelial cells, signifying the possible existence of a progenitor cell population. By combining the information on marker expression and in situ localization with immunomagnetic sorting and subsequent immortalization, we have identified and isolated a cytokeratin 19-positive suprabasal putative precursor cell in the luminal epithelial compartment and established representative cell lines. This suprabasal-derived epithelial cell line is able to generate both itself and differentiated luminal epithelial and myoepithelial cells, and in addition, is able to form elaborate terminal duct lobular unit (TDLU)-like structures within a reconstituted basement membrane. As more than 90% of breast cancers arise in TDLUs and more than 90% are also cytokeratin 19-positive, we suggest that this cell population contains a breast-cancer progenitor.

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Year:  2003        PMID: 14521514      PMCID: PMC2933221          DOI: 10.1046/j.1365-2184.36.s.1.4.x

Source DB:  PubMed          Journal:  Cell Prolif        ISSN: 0960-7722            Impact factor:   6.831


  60 in total

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8.  EGF controls the in vivo developmental potential of a mammary epithelial cell line possessing progenitor properties.

Authors:  Marie-Ange Deugnier; Marisa M Faraldo; Bassam Janji; Patricia Rousselle; Jean Paul Thiery; Marina A Glukhova
Journal:  J Cell Biol       Date:  2002-11-11       Impact factor: 10.539

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10.  Functional and molecular characterisation of mammary side population cells.

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2.  Localization of putative stem cells and four cell populations with different differentiation degree in mouse mammary anlagen.

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3.  Caveolin-1 mutations in human breast cancer: functional association with estrogen receptor alpha-positive status.

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Review 4.  Maintenance of cell type diversification in the human breast.

Authors:  Agla Jael Rubner Fridriksdottir; René Villadsen; Thorarinn Gudjonsson; Ole William Petersen
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6.  Immortalization of epithelial progenitor cells mediated by resveratrol.

Authors:  V P Pearce; J Sherrell; Z Lou; L Kopelovich; W E Wright; J W Shay
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7.  Cellular heterogeneity profiling by hyaluronan probes reveals an invasive but slow-growing breast tumor subset.

Authors:  Mandana Veiseh; Daniel H Kwon; Alexander D Borowsky; Cornelia Tolg; Hon S Leong; John D Lewis; Eva A Turley; Mina J Bissell
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Review 9.  Myoepithelial cells: their origin and function in breast morphogenesis and neoplasia.

Authors:  Thorarinn Gudjonsson; Melissa C Adriance; Mark D Sternlicht; Ole W Petersen; Mina J Bissell
Journal:  J Mammary Gland Biol Neoplasia       Date:  2005-07       Impact factor: 2.673

Review 10.  Intrauterine breast development and the mammary myoepithelial lineage.

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Journal:  J Mammary Gland Biol Neoplasia       Date:  2005-07       Impact factor: 2.698

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