su-1498 and Corneal-Neovascularization

su-1498 has been researched along with Corneal-Neovascularization* in 1 studies

Other Studies

1 other study(ies) available for su-1498 and Corneal-Neovascularization

ArticleYear
Suppression of pathological ocular neovascularization by a small molecule, SU1498.
    Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 2020, Volume: 128

    Selective inhibition of vascular endothelial growth factor receptor (VEGFR), particularly VEGFR-2, is an efficient method for the treatment of ocular neovascularization. SU1498 is a specific inhibitor of VEGFR-2. In this study, we investigated the role of SU1498 in ocular neovascularization. Administration of SU1498 did not show any cytotoxicity and tissue toxicity at the tested concentrations. Administration of SU1498 reduced the size and thickness of choroidal neovascularization and decreased the mean length and mean number of corneal neovascular vessels induced by alkali burn. Pretreatment of SU1498 significantly reduced the proliferation, migration, and tube formation ability of HUVECs. SU1498 played the anti-angiogenic role through the regulation of p38-MAPK signaling. Taken together, inhibition of VEGFR-2 by SU1498 provides a novel therapeutic approach for ocular neovascularization.

    Topics: Angiogenesis Inhibitors; Animals; Cell Movement; Cell Proliferation; Cells, Cultured; Choroid; Choroidal Neovascularization; Cinnamates; Cornea; Corneal Neovascularization; Disease Models, Animal; Endothelial Cells; Human Umbilical Vein Endothelial Cells; Humans; Male; Mice, Inbred C57BL; Neovascularization, Physiologic; Signal Transduction; Vascular Endothelial Growth Factor Receptor-2

2020