PMID- 7989454 OWN - NLM STAT- MEDLINE DCOM- 19950112 LR - 20161123 IS - 0021-972X (Print) IS - 0021-972X (Linking) VI - 79 IP - 6 DP - 1994 Dec TI - Circulating fibroblast growth factor-like autoantibodies in two patients with multiple endocrine neoplasia type 1 and prolactinoma. PG - 1546-52 AB - Basic fibroblast growth factor (bFGF) is a potent endothelial cell mitogen found in a variety of normal and tumor tissues. bFGF lacks a classical amino-terminal signal sequence and is not readily detectable in plasma from normal subjects. In earlier studies we showed increased bFGF-like mitogenic activity for parathyroid-derived endothelial cells and (increased) bFGF immunoreactivity (0.24-1.28 ng/mL) in plasma of subjects with multiple endocrine neoplasia type 1 (MEN-1). In the present study we examined the proliferative activity of MEN-1 and normal plasmas (applied to protein-A columns) in calf pulmonary artery endothelial cells. Protein-A-eluted activity in plasma from MEN-1 prolactinoma plasma exceeded activity from normal and MEN-1 nonprolactinoma plasma in three of eight MEN-1 subjects with untreated or recurrent prolactinoma. Protein-A-eluted active fractions from MEN-1 prolactinoma plasma had several properties of an immunoglobulin G, including affinity for antihuman immunoglobulin G (IgG) agarose, sensitivity to thiols, and (prepared by sodium dodecyl sulfate-polyacrylamide gel electrophoresis under reducing conditions) apparent mol wt corresponding to those of the heavy and light chains of IgG. The IgG fraction of MEN-1 prolactinoma plasma had far more activity in endothelial cells than did optimal concentrations of known growth factors or conditioned medium from prolactinoma cells. Endothelial cell bioactivity in protein-A-eluted fractions from MEN-1 prolactinoma plasma was neutralized 70% by rabbit antibodies to intact bFGF. These results imply novel growth stimulatory bFGF-like autoantibodies in a subset of MEN-1 patients with prolactinoma. FAU - Zimering, M B AU - Zimering MB AD - Veterans Affairs Medical Center, Lyons, New Jersey 07939. FAU - Riley, D J AU - Riley DJ FAU - Thakker-Varia, S AU - Thakker-Varia S FAU - Walker, A M AU - Walker AM FAU - Lakshminaryan, V AU - Lakshminaryan V FAU - Shah, R AU - Shah R FAU - Brandi, M L AU - Brandi ML FAU - Ezzat, S AU - Ezzat S FAU - Katsumata, N AU - Katsumata N FAU - Friesen, H G AU - Friesen HG AU - et al. LA - eng PT - Case Reports PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - J Clin Endocrinol Metab JT - The Journal of clinical endocrinology and metabolism JID - 0375362 RN - 0 (Autoantibodies) RN - 0 (Immunoglobulin G) RN - 0 (Staphylococcal Protein A) RN - 103107-01-3 (Fibroblast Growth Factor 2) SB - IM MH - Adult MH - Animals MH - Autoantibodies/*blood MH - Cattle MH - Cell Division/drug effects MH - Chemical Phenomena MH - Chemistry, Physical MH - Chromatography, Affinity MH - Endothelium, Vascular/*cytology MH - Female MH - Fibroblast Growth Factor 2/*immunology MH - Humans MH - Immunoglobulin G/blood/chemistry/pharmacology MH - Male MH - Middle Aged MH - Multiple Endocrine Neoplasia/*immunology MH - Pituitary Neoplasms/*immunology MH - Prolactinoma/*immunology MH - Rats MH - Staphylococcal Protein A MH - Tumor Cells, Cultured EDAT- 1994/12/01 00:00 MHDA- 1994/12/01 00:01 CRDT- 1994/12/01 00:00 PHST- 1994/12/01 00:00 [pubmed] PHST- 1994/12/01 00:01 [medline] PHST- 1994/12/01 00:00 [entrez] AID - 10.1210/jcem.79.6.7989454 [doi] PST - ppublish SO - J Clin Endocrinol Metab. 1994 Dec;79(6):1546-52. doi: 10.1210/jcem.79.6.7989454.