Institute of Chinese Medicine, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong.
Eur J Med Chem. 2013 Jan;59:243-52. doi: 10.1016/j.ejmech.2012.11.029. Epub 2012 Nov 24.
Bigelovin is a sesquiterpene lactone isolated from the plant Inula helianthus-aquatica which was traditionally used in cancer treatment in Yunnan, China. The potent apoptotic activities of bigelovin in human leukemia U937 cells were shown in our previous study. The present study investigated the anti-angiogenic and immunomodulatory effects of bigelovin using transgenic zebrafish Tg(fli1a:EGFP)y1 with fluorescent blood vessels and human peripheral blood mononuclear cells (PBMCs), respectively. Furthermore, the inhibitory activities of bigelovin on the human endothelial cell adhesion molecules (CAMs) were also examined. Our results showed that the growth of subintestinal vessels of the bigelovin-treated zebrafish embryos was significantly inhibited and the gene expressions in angiogenesis signaling pathways (e.g. Ang2 and Tie2) of the zebrafish were down-regulated after bigelovin treatment. Besides, the proliferation and Th1 cytokines productions (e.g. IFN-γ, IL-2 and IL-12) were suppressed in bigelovin-treated PBMCs. On the other hand, bigelovin was shown to significantly inhibit the human monocyte adhesion to human endothelial cells and the gene expressions of inflammation-related CAMs (e.g. ICAM-1, VCAM-1 and E-selectin) were significantly down-regulated in bigelovin-treated human endothelial cells. In summary, our data provide the first evidence that bigelovin possesses anti-angiogenic and immunomodulatory activities, suggesting bigelovin may exert multi-target functions against cancer in animal models.
比格尔文是从中国云南传统上用于癌症治疗的植物旋覆花中分离得到的一种倍半萜内酯。在我们之前的研究中,已经证明了比格尔文在人白血病 U937 细胞中具有很强的凋亡活性。本研究分别利用转荧光血管的转基因斑马鱼 Tg(fli1a:EGFP)y1 和人外周血单核细胞(PBMCs)研究了比格尔文的抗血管生成和免疫调节作用。此外,还研究了比格尔文对人内皮细胞黏附分子(CAMs)的抑制活性。结果表明,比格尔文处理的斑马鱼胚胎的次级肠血管生长受到明显抑制,比格尔文处理后斑马鱼的血管生成信号通路(如 Ang2 和 Tie2)的基因表达下调。此外,比格尔文处理的 PBMCs 的增殖和 Th1 细胞因子(如 IFN-γ、IL-2 和 IL-12)的产生受到抑制。另一方面,比格尔文显著抑制人单核细胞与人内皮细胞的黏附,并且在比格尔文处理的人内皮细胞中,炎症相关的 CAMs(如 ICAM-1、VCAM-1 和 E-选择素)的基因表达显著下调。总之,我们的数据首次提供了比格尔文具有抗血管生成和免疫调节活性的证据,表明比格尔文可能在动物模型中通过多靶点发挥抗肿瘤作用。