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Division of Biological Sciences, Harvard School of Public Health [N. M. S., M. B., P. P., H. N. A.]; Laboratory of Clinical Pharmacology, Dana Farber Cancer Institute, Harvard Medical School [E. S.]; and the Center for Blood Research [P. P., H. N. A.], Boston, Massachusetts 02115
Prostate carcinoma cell lines DU-145 and PC-3 express both platelet derived growth factor (PDGF)-1 and PDGF-2/sis genes. Concomitantly, these cells synthesize and secrete PDGF-like proteins, as judged by indirect immunofluorescence and by direct immunoprecipitation with specific PDGF antiserum. Conditioned media derived from DU-145 and PC-3 cells stimulated the incorporation of [3H]thymidine by 3T3 cells and competed with 125I-labeled PDGF for its binding to cell surface receptors of 3T3 cells. The biological activity was stable to heating at 100°C for 10 min, sensitive to reducing agents, and neutralized by the IgG fraction of PDGF antiserum, properties similar to those of authentic PDGF. Both DU-145 and PC-3 cell lines appear to lack receptors for PDGF as indicated by their inability to mitogenically respond to PDGF and receptor binding of 125I-labeled PDGF. Production of PDGF-like proteins by human prostate carcinoma cells may play an important role in a paracrine mode in the organization of the extracellular matrix of the malignant tissue.
1 Supported by USPHS Grants CA38784 (P. P.), CA30101, and HL29583 (H. N. A.) and by the Council for Tobacco Research (H. N. A.).
2 Fellow of the National Council of Science and Technology of Mexico ("CONACYT").
3 To whom requests for reprints should be addressed.
Received 8/25/87. Revised 12/23/87. Accepted 1/ 6/88.
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