Bloom's syndrome cells have an abnormal serum growth response |
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Authors: | John F. Lechner M. Edward Kaighn Anton M. Jetten Joanna Groden James German |
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Affiliation: | 1. Laboratory of Human Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, MD 20205 USA;2. Laboratory of Experimental Pathology, National Cancer Institute-FCRF, National Institutes of Health, Frederick, MD 21701 USA;3. Laboratory of Cellular Carcinogenesis and Tumor Promotion, National Cancer Institute, National Institutes of Health, Bethesda, MD 20205 USA;4. The New York Blood Center, New York, NY 10021, USA |
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Abstract: | ![]() Certain growth responses of Bloom's syndrome (BS) dermal fibroblasts have been compared to those of normal human fibroblasts. By applying the principles of Michaelis-Menton kinetics to clonal dose-response data, serum and epidermal growth factor (EGF) requirements of the two cell types were found to be similar. However, the maximal clonal growth rate of BS cells was significantly lower than that of their normal counterparts. Although specific EGF binding by BS cells was marginally higher than in normal cells, EGF's growth-promoting activity was only half of that seen in normal cells. These observations indicate that the abnormally low growth rate of BS cells is not attributable to excessive requirements for serum-derived growth factors and suggest instead that the genetic defect in some way impairs the cells' ability to respond fully to growth stimulation. |
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Keywords: | To whom offprint requests should be addressed. |
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