Department of Biotechnology, Translational Research Center for Protein Function Control, Yonsei University, Seoul, Republic of Korea.
Biochem Biophys Res Commun. 2010 Aug 13;399(1):20-3. doi: 10.1016/j.bbrc.2010.07.025. Epub 2010 Jul 17.
R-(-)-beta-O-methylsynephrine (OMe-Syn) is an active compound isolated from a plant of the Rutaceae family. We conducted cell proliferation assays on various cell lines and found that OMe-Syn more strongly inhibited the growth of human umbilical vein endothelial cells (HUVECs) than that of other normal and cancer cell lines tested. In angiogenesis assays, it inhibited vascular endothelial growth factor (VEGF)-induced invasion and tube formation of HUVECs with no toxicity. The anti-angiogenic activity of OMe-Syn was also validated in vivo using the chorioallantonic membrane (CAM) assay in growing chick embryos. Expression of the growth factors VEGF, hepatocyte growth factor, and basic fibroblast growth factor was suppressed by OMe-Syn in a dose-dependent manner. Taken together, our results indicate that this compound could be a novel basis for a small molecule targeting angiogenesis.
R-(-)-β-甲氧基去甲肾上腺素(OMe-Syn)是从芸香科植物中分离得到的一种活性化合物。我们在各种细胞系上进行了细胞增殖实验,发现 OMe-Syn 比其他测试的正常和癌细胞系更强烈地抑制人脐静脉内皮细胞(HUVEC)的生长。在血管生成实验中,它抑制了血管内皮生长因子(VEGF)诱导的 HUVEC 的侵袭和管形成,且没有毒性。OMe-Syn 的抗血管生成活性也在鸡胚绒毛尿囊膜(CAM)实验中得到了体内验证。生长因子 VEGF、肝细胞生长因子和碱性成纤维细胞生长因子的表达被 OMe-Syn 以剂量依赖的方式抑制。综上所述,我们的结果表明,这种化合物可能成为一种针对血管生成的小分子的新基础。