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Research Article

The mouse Wnt-1 gene can act via a paracrine mechanism in transformation of mammary epithelial cells.

S F Jue, R S Bradley, J A Rudnicki, H E Varmus, A M Brown
S F Jue
Department of Cell Biology and Anatomy, Cornell University Medical College, New York, New York 10021.
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R S Bradley
Department of Cell Biology and Anatomy, Cornell University Medical College, New York, New York 10021.
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J A Rudnicki
Department of Cell Biology and Anatomy, Cornell University Medical College, New York, New York 10021.
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H E Varmus
Department of Cell Biology and Anatomy, Cornell University Medical College, New York, New York 10021.
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A M Brown
Department of Cell Biology and Anatomy, Cornell University Medical College, New York, New York 10021.
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DOI: 10.1128/MCB.12.1.321
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ABSTRACT

The mouse Wnt-1 gene plays an essential role in fetal brain development and can contribute to tumorigenesis when activated aberrantly in the mammary gland. The gene encodes secretory glycoproteins associated with the extracellular or pericellular matrix, and it has been proposed that Wnt-1, as well as its Drosophila homolog wingless, may function in intercellular signalling. We show here that fibroblasts expressing Wnt-1 protein, although not transformed themselves, are able to elicit morphological transformation of neighboring C57MG mammary epithelial cells in coculture experiments. Heparin inhibits this effect, possibly by displacing Wnt-1 protein from its normal site of action. Our results indicate that the Wnt-1 gene can act via a paracrine mechanism in cell culture and strongly support the notion that in vivo the gene may function in cell-to-cell communication.

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The mouse Wnt-1 gene can act via a paracrine mechanism in transformation of mammary epithelial cells.
S F Jue, R S Bradley, J A Rudnicki, H E Varmus, A M Brown
Molecular and Cellular Biology Jan 1992, 12 (1) 321-328; DOI: 10.1128/MCB.12.1.321

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The mouse Wnt-1 gene can act via a paracrine mechanism in transformation of mammary epithelial cells.
S F Jue, R S Bradley, J A Rudnicki, H E Varmus, A M Brown
Molecular and Cellular Biology Jan 1992, 12 (1) 321-328; DOI: 10.1128/MCB.12.1.321
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