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The Syk tyrosine kinase suppresses malignant growth of human breast cancer cells

Author

Listed:
  • Peter J. P. Coopman

    (Department of Cell Biology
    Centre National de la Recherche Scientifique UMR 5539)

  • Michael T. H. Do

    (Department of Cell Biology)

  • Mara Barth

    (Department of Cell Biology)

  • Emma T. Bowden

    (Department of Oncology)

  • Andrew J. Hayes

    (Department of Oncology)

  • Eugenia Basyuk

    (Centre National de la Recherche Scientifique UPR 9023)

  • Jan K. Blancato

    (Georgetown University Medical School)

  • Phyllis R. Vezza

    (Department of Pathology)

  • Sandra W. McLeskey

    (Department of Oncology
    Department of Pharmacology and School of Nursing)

  • Paul H. Mangeat

    (Centre National de la Recherche Scientifique UMR 5539)

  • Susette C. Mueller

    (Department of Cell Biology
    Department of Oncology)

Abstract

Syk is a protein tyrosine kinase that is widely expressed in haematopoietic cells. It is involved in coupling activated immunoreceptors to downstream signalling events that mediate diverse cellular responses including proliferation, differentiation and phagocytosis1,2,3,4. Syk expression has been reported in cell lines of epithelial origin5, but its function in these cells remains unknown. Here we show that Syk is commonly expressed in normal human breast tissue, benign breast lesions and low-tumorigenic breast cancer cell lines. Syk messenger RNA and protein, however, are low or undetectable in invasive breast carcinoma tissue and cell lines. Transfection of wild-type Syk into a Syk-negative breast cancer cell line markedly inhibited its tumour growth and metastasis formation in athymic mice. Conversely, overexpression of a kinase-deficient Syk in a Syk-positive breast cancer cell line significantly increased its tumour incidence and growth. Suppression of tumour growth by the reintroduction of Syk appeared to be the result of aberrant mitosis and cytokinesis. We propose that Syk is a potent modulator of epithelial cell growth and a potential tumour suppressor in human breast carcinomas.

Suggested Citation

  • Peter J. P. Coopman & Michael T. H. Do & Mara Barth & Emma T. Bowden & Andrew J. Hayes & Eugenia Basyuk & Jan K. Blancato & Phyllis R. Vezza & Sandra W. McLeskey & Paul H. Mangeat & Susette C. Mueller, 2000. "The Syk tyrosine kinase suppresses malignant growth of human breast cancer cells," Nature, Nature, vol. 406(6797), pages 742-747, August.
  • Handle: RePEc:nat:nature:v:406:y:2000:i:6797:d:10.1038_35021086
    DOI: 10.1038/35021086
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    Cited by:

    1. Aurélien Naldi & Romain M Larive & Urszula Czerwinska & Serge Urbach & Philippe Montcourrier & Christian Roy & Jérôme Solassol & Gilles Freiss & Peter J Coopman & Ovidiu Radulescu, 2017. "Reconstruction and signal propagation analysis of the Syk signaling network in breast cancer cells," PLOS Computational Biology, Public Library of Science, vol. 13(3), pages 1-27, March.

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