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[Cancer Research 52, 341-347, January 15, 1992]
© 1992 American Association for Cancer Research

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Transforming Growth Factor-{alpha} Acts as an Autocrine Growth Factor in Ovarian Carcinoma Cell Lines

Kurt Stromberg1, Theodore J. Collins, IV, Alfred W. Gordon, Carolyn L. Jackson and Gibbes R. Johnson

Laboratory of Cell Biology, Division of Cytokine Biology, Food and Drug Administration, Bethesda, Maryland 20892

The potential of transforming growth factor-{alpha} (TGF-{alpha}) to function as an autocrine growth factor was evaluated in numerous ovarian carcinoma cell lines. All 17 lines which were examined expressed the epidermal growth factor receptor and 16 cell lines, in addition, concomitantly secreted TGF-{alpha}. Radioimmunoassay of processed serum-free-conditioned medium indicated TGF-{alpha} concentrations ranging from 16 to 197 pg/ml, or 1.5 to 95 ng/108 cells. 125I-TGF-{alpha} bound to a single class of high-affinity-binding sites on the surface of the cells. The dissociation constant for the 125I-TGF-{alpha}/epidermal growth factor receptor complex ranged from 0.21 to 5.3 nM with receptor numbers from 3,500 to 96,000/cell, depending upon the cell line. The growth of 8 ovarian cell lines was stimulated in a dose-dependent manner when grown in the presence of exogenous TGF-{alpha}. Growth in 4 of 5 cell lines capable of serum-free propagation was inhibited from 28 to 56% when cultured in medium containing a TGF-{alpha}-neutralizing monoclonal antibody. These results support the view that TGF-{alpha} is an autocrine growth factor for cell lines derived from ovarian cancers of epithelial origin and suggest a potential role for TGF-{alpha} in the pathogenesis or progression of the disease.

1 To whom requests for reprints should be addressed, at the Food and Drug Administration, HFB-830, Building 29A, Room 2B-08, 8800 Rockville Pike, Bethesda, MD 20892.

Received 7/ 8/91. Accepted 10/31/91.




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Copyright © 1992 by the American Association for Cancer Research.