Type β Transforming Growth Factor: A Bifunctional Regulator of Cellular Growth

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 82; no. 1; pp. 119 - 123
• Main Authors: Roberts, Anita B., Anzano, Mario A., Wakefield, Lalage M., Roche, Nanette S., Stern, David F., Sporn, Michael B.
• Format: Journal Article
• Language: English
• Published: Washington, DC National Academy of Sciences of the United States of America 01.01.1985; National Acad Sciences
• Subjects: Animals; Biological and medical sciences; Cell Adhesion; Cell Cycle - drug effects; Cell growth; Cell Line; Cell lines; Cell physiology; Cell Transformation, Viral; Cells, Cultured; Cultured cells; Drug Interactions; Epidermal Growth Factor - pharmacology; Epithelial cells; Fibroblasts; Fibroblasts - cytology; Fundamental and applied biological sciences. Psychology; Growth Inhibitors - pharmacology; Growth Substances - pharmacology; Human growth; Kidney cells; Lungs; Melanoma; Molecular and cellular biology; Oncogenes; Peptides - pharmacology; Rats; Responses to growth factors, tumor promotors, other factors; Transforming Growth Factors; Tumor cell line; Cell proliferation; Cell culture; Vertebrata; Fixation; Mammalia; Animal; Modulation; Cell transformation; Biological activity; Tumor cell; Growth factor
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.82.1.119

Type β transforming growth factor (TGF-β ) is a two-chain polypeptide of 25,000 daltons isolated from many tissues, including bovine kidney, human placenta, and human platelets. It has been characterized by its ability to stimulate reversible transformation of nonneoplastic murine fibroblasts, as measured by the formation of colonies of these cells in soft agar (ED50= 4 pM TGF-β for NRK fibroblasts). We now show that the response of cells to TGF-β is bifunctional, in that TGF-β inhibits the anchorage-dependent growth of NRK fibroblasts and of human tumor cells by increasing cell cycle time. Moreover, the anchorage-independent growth of many human melanoma, lung carcinoma, and breast carcinoma cell lines is inhibited by TGF-β at concentrations in the same range as those that stimulate colony formation of NRK fibroblasts (average ED50= 10-30 pM TGF-β for inhibition). Whereas epidermal growth factor and TGF-β synergize to induce anchorage-independent growth of NRK fibroblasts, their effects on the growth of A-549 human lung carcinoma cells are antagonistic. The bifunctional response of cells to TGF-β is further demonstrated in Fischer rat 3T3 fibroblasts transfected with a cellular myc gene. In these cells TGF-β synergizes with platelet-derived growth factor to stimulate colony formation but inhibits the colony formation induced by epidermal growth factor. The data indicate that the effects of TGF-β on cells are not a function of the peptide itself, but rather of the total set of growth factors and their receptors that is operant in the cell at a given time.