Stimulation of Bone Resorption in Vitro by Synthetic Transforming Growth Factor-Alpha
- 24 May 1985
- journal article
- research article
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 228 (4702), 1007-1009
- https://doi.org/10.1126/science.3859011
Abstract
Experiments were conducted to test the hypothesis that tumor-derived transforming growth factor-alpha (TGF-alpha) is responsible for the increased bone resorption and hypercalcemia seen in some malignant diseases. Homogeneous synthetic TGF-alpha prepared by the solid-phase synthesis method stimulated bone resorption directly in vitro in a concentration-dependent manner. Incubation times of 72 hours or more were required to stimulate resorption, which is similar to the time course of bone resorption by epidermal growth factor.This publication has 12 references indexed in Scilit:
- EGF RECEPTOR ANTISERUM INHIBITS BONE RESORBING ACTIVITY PRODUCED BY A RAT LEYDIG CELL TUMOR ASSOCIATED WITH THE HUMORAL HYPERCALCEMIA OF MALIGNANCYEndocrinology, 1985
- Human transforming growth factor-α: Precursor structure and expression in E. coliCell, 1984
- Synthesis of biologically active rat transforming growth factor INature, 1984
- Tumor-Derived Growth Factor Increases Bone Resorption in a Tumor Associated with Humoral Hypercalcemia of MalignancyScience, 1983
- Human transforming growth factor. Production by a melanoma cell line, purification, and initial characterization.Journal of Biological Chemistry, 1982
- Autocrine Secretion and Malignant Transformation of CellsNew England Journal of Medicine, 1980
- lDirect Stimulation of Bone Resorption by Epidermal Growth Factor*Endocrinology, 1980
- Epidermal growth factor stimulates prostaglandin production and bone resorption in cultured mouse calvariaBiochemical and Biophysical Research Communications, 1978
- Transformation by murine and feline sarcoma viruses specifically blocks binding of epidermal growth factor to cellsNature, 1976
- Bone Resorption in Tissue Culture. Factors Influencing the Response to Parathyroid Hormone *Journal of Clinical Investigation, 1965