Early Research Suggests that Understanding the Fundamental Mechanism of Angiogenesis is More Complicated Than Understanding the Function of VEGF - A
Amgen Launches Angiogenesis Website
    THOUSAND OAKS, Calif., 
Data will be presented on investigational compounds AMG 386, a peptibody that binds to and inhibits angiopoietins 1 and 2; AMG 479, a fully human monoclonal antibody antagonist of the type 1 insulin-like growth factor receptor (IGF-1R) and AMG 102, a fully human monoclonal antibody antagonist of HGF, the ligand for the c-Met receptor.
    "The data being presented at this meeting further our biologic
understanding of these novel compounds and pathways, and inform our thinking
regarding opportunities to develop predictive or prognostic biomarkers," said
 
    Selected Abstracts of Interest 
    --  Assessment of angiogenesis inhibitors in the retinopathy of
        prematurity model in mice
        Overview: Examined the inhibition of the VEGF/VEGFR pathway with AMG
        273 and the inhibition of the angiopoietin/Tie2 pathway with AMG 386
        Lead author: Estrada J.
        Abstract No. 140 (
    --  Involvement of the CSF-1/CSF-1R interaction in the control of
        angiogenesis
        Overview: Two different neutralizing rat anti murine CSF-1R monoclonal
        antibodies (mAb), M279 and AFS98 were evaluated for their effect on
        mouse corneal angiogenesis and corneal macrophage recruitment in vivo
        Lead author: Liu H.
        Abstract No. 1106 (
    --  Complementary and opposing effects of angiopoietin-1 and
        angiopoietin-2 inhibitors on tumor blood vessels and normalization
        Overview: Aimed to elucidate the effects of Angiopoietin (Ang) 1 and
        Ang2 on the tumor vasculature of a human colon carcinoma model
        (Colo205) using peptide-Fc fusion proteins (peptibodies) specifically
        targeting Ang1 (mL4-3) or Ang2 (L1-7(N)) alone or in combination
        Lead author: Falcon B.
        Abstract No. 1996 (
    --  AMG 479, a novel IGF-1R antibody, inhibits endometrial cancer cell
        proliferation through disruption of the P13K/Akt and MAPK pathways
        Overview: Evaluated the effect of a novel antibody to the IGF-1R (AMG
        479) on cell proliferation and expression of key targets involved in
        IGF-1R signaling in endometrial cancer cells
        Lead author: Mendivil A.
        Abstract No. 2804 (
    --  AMG 479, a fully human anti-IGF-1R monoclonal antibody, inhibits
        rapamycin-induced Akt activation in sarcoma cell lines
        Overview: Evaluated whether AMG 479 could inhibit this feedback-loop
        mechanism and thus increase the efficacy of rapamycin and its analogs
        (mTOR inhibitors). 
        Lead author: Beltran P.
        Abstract No. 2805 (
    --  Dual targeting of the receptor tyrosine kinase EGFRvIII and HGF:c-Met
        signaling in models of glioblastoma multiforme (GBM)
        Overview: Examined the effect of combining a fully human neutralizing
        antibody targeting the HGF:c-Met axis (AMG 102), with a fully human
        antibody binding to the EGFR and EGFRvIII (panitumumab) to overcome
        resistance to HGF:c-Met based therapeutic strategies in GBM
        Lead author: Johns T.
        Abstract No. 2044 (
    --  Antagonistic antibodies to c-fms block c-fms-mediated activities,
        reduce tumor-associated macrophages and decrease tumor growth in
        preclinical models
        Overview: Antagonistic antibodies to c-fms were evaluated for their
        effects on monocytic cell function in vitro and tumor-associated
        macrophages (TAMs) and tumor growth in vivo
        Lead author: Bonham L.
        Abstract No. 2077 (
    --  Erythropoietin Receptor (EpoR) Was Expressed at Low to Undetectable
        Levels in Tumor Cell Lines: Expression Was Not Regulated by Hypoxia
        and No Epo-Induced Downstream Signaling Was Detectable
        Overview: EpoR, mRNA and protein expression were surveyed in 67
        tumor-derived cell lines from ovary, breast, head and neck, lung,
        brain, prostate, cervix, liver, colon and blood
        Lead author: Swift S.
        Abstract No. 4283 (
    Amgen Launches Educational Interactive Angiogenesis Website
    
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