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

被引:0
|
作者
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
机构
[1] Department of Cell Biology,Institute for Molecular and Human Genetics, and Vincent T. Lombardi Cancer Center
[2] Department of Oncology,undefined
[3] Department of Pathology,undefined
[4] Department of Pharmacology and School of Nursing,undefined
[5] Georgetown University Medical School,undefined
[6] Centre National de la Recherche Scientifique UPR 9023,undefined
[7] Centre National de la Recherche Scientifique UMR 5539,undefined
[8] Centre National de la Recherche Scientifique UMR 5539,undefined
来源
Nature | 2000年 / 406卷
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摘要
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.
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页码:742 / 747
页数:5
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