Chitnis MM, Yuen JS, Protheroe AS, Pollak M, Macaulay VM

Chitnis MM, Yuen JS, Protheroe AS, Pollak M, Macaulay VM. Receptor binding antibodies suppressed IGF-1 stimulation of Akt phosphorylation, but IGF-2 circumvented this effect and maintained HUVEC tube formation. MEDI-573 inhibited HUVEC proliferation and tube formation the anti-angiogenic activity of MEDI-573 was also circumvented by human recombinant IGF-1. The combination of receptor- and ligand-binding antibodies completely suppressed VEGF-stimulated proliferation of HUVECs in the presence of IGF-1 and IGF-2, prevented ligand-induced phosphorylation of IGF-1R/IR receptors, and suppressed VEGF/IGF-2 driven angiogenesis (5, 6), and inhibited the growth of rhabdomyosarcoma xenografts (7). IGF-1R and its Tyrphostin A1 ligands play roles not only in tumor cell proliferation and survival, but also in tumor angiogenesis (8). Two studies have suggested that IGF-1R antibodies exert a strong effect on tumor angiogenesis (6, 9). Our data showed anti-angiogenic activity of IGF-1R-binding antibody (SCH717454) both and but IGF-2 circumvented these effects (10). Many childhood cancers secrete IGF-2, suggesting that tumor-derived IGF-2 can promote angiogenesis in the presence of IGF-1R-targeted antibodies through binding to the insulin receptor (IR) permitting continued tumor growth. Several studies have reported overexpression of IGF2 in sarcoma cell lines as well as in primary tumors (5, 11-13). Currently there are both small molecule drugs and fully human or humanized antibodies directed at the IGF-1R. Five fully human (CP-751871, AMG 479, R1507, IMC-A12, SCH717454) or humanized antibodies (H7C10/MK0646) have been evaluated in adult phase-I to -III clinical trials. These agents show specificity for IGF-IR although they may inhibit chimeric receptors formed through hetero-dimerization with the insulin receptor (IR). However, Tyrphostin A1 in xenograft models of childhood tumors associated with IGF-dysregulation, these antibodies induce only rare tumor regressions (6, 14, 15), consistent with the relatively low response rate of Ewing sarcoma patients to figitumumab (CP751871) (16). Intrinsic resistance may be a consequence of maintained signaling by IGF-2 through the IR (8, 10, 17, 18). The aim of this study was to evaluate the anti-angiogenic activity of an IGF-ligand Tyrphostin A1 binding antibody (MEDI-573) alone, or combined with IGF-1R receptor-binding antibodies. This is the first report showing the anti-angiogenic activity of the ligand-neutralizing antibody MEDI-573, and reversal of activity by exogenous IGF-1. Our results also demonstrate that, both and in a mouse model, combined inhibition of IGF-1R and its ligands (IGF1/2) abrogates angiogenesis in the presence of exogenous IGF’s. Targeting angiogenesis by inhibiting both IGF-1R and IGFs through use of dual antibodies may therefore be an effective Rabbit Polyclonal to ELOVL3 anti-angiogenic strategy in pediatric sarcomas. MATERIALS AND Tyrphostin A1 METHODS Reagents Medium 200, fetal bovine serum (FBS) and Alamar Blue (AB) were purchased from Invitrogen (Carlsbad, CA). Low serum growth supplement (LSGS) was obtained from Cascade Biologics Inc (Portland Oregon). Endothelial Tube formation assay kits were from Cell Biolabs, Inc. (San Diego, CA). Growth factorCreduced Matrigel for experiments and precoated Matrigel inserts for invasion assays were purchased from BD Biosciences (Palo Alto, CA). MedImmune generously provided MEDI-573 and CP1-B02 antibodies and MAB391 antibody was purchased from R&D Systems. MEDI-573 binds human IGF-2 with high affinity, while its affinity for human IGF-1 is lower, and affinity for murine IGF-1 is very low (19). CP1-B02 and MAB391 antibodies bind the IGF-1 receptor, preventing ligand binding. Human recombinant IGF-1 and IGF-2 were purchased from PeproTech Inc., NJ. BMS754807 was purchased through Selleckchem.com. Cell Culture Human umbilical vein endothelial cells (HUVEC) were obtained from the American Type Culture Collection (ATCC). All experiments were done using endothelial cells Tyrphostin A1 between passages 3 and 8. HUVECs were maintained in medium M200 (Invitrogen) with 15% fetal bovine serum (FBS), endothelial cell growth supplements (LSGS Medium, Cascade Biologics), and 2 mM glutamine at 37C with 5% CO2. All cells were maintained as sub confluent cultures and split 1:3, 24 hr before use. Rhabdomyosarcoma cell lines were cultured in RPMI 1640 supplemented with 10% FBS. Western blotting Cell lysis, protein extraction and immunoblotting were as described previously (6, 9). We used primary antibodies to glyceraldehyde-3-phosphate dehydrogenase (GAPDH), AKT, phospho-AKT (Ser473), IGF-1R, and phospho-IGF-1R (Tyr1131), IR and phosphor-IR (Tyr1146) (Cell Signaling). Immunoreactive bands were visualized by using Super Signal Chemiluminiscence substrate (Pierce, Rockford, IL) and Biomax MR and XAR film (Eastman Kodak Co., Rochester, NY). Immuno-precipitations were performed by adding either 2g of IGF-1R antibody (Santa Cruz biotechnology Inc., Sant Cruz, CA). Fifteen L of total.