Graduate School of Nutritional and Environmental Sciences and Global COE Program, University of Shizuoka, Shizuoka 422-8526, Japan.
Evid Based Complement Alternat Med. 2011;2011:870753. doi: 10.1093/ecam/nep024. Epub 2010 Oct 31.
We recently reported that propolis suppresses tumor-induced angiogenesis through tube formation inhibition and apoptosis induction in endothelial cells. However, molecular mechanisms underlying such angiogenesis suppression by propolis have not been fully elucidated. The aim of this study was to investigate the effects of ethanol extract of Brazilian propolis (EEBP) on two major survival signals, extracellular signal-regulated kinase 1/2 (ERK1/2) and Akt, and to elucidate whether changes in these signals were actually involved in antiangiogenic effects of the propolis. Detection by western blotting revealed that EEBP suppressed phosphorylation of ERK1/2, but not that of Akt. Pharmacological inhibition by U0126 demonstrated that ERK1/2 inactivation alone was enough to inhibit tube formation and induce apoptosis. It was also shown that EEBP and U0126 similarly induced activation of caspase-3 and cleavage of poly ADP-ribose polymerase (PARP) and lamin A/C, all of which are molecular markers of apoptosis. These results indicate that inhibition of survival signal ERK1/2, and subsequent induction of apoptosis, is a critical mechanism of angiogenesis suppression by EEBP.
我们最近报道称,蜂胶通过抑制内皮细胞的管腔形成和诱导细胞凋亡来抑制肿瘤诱导的血管生成。然而,蜂胶抑制血管生成的分子机制尚未完全阐明。本研究旨在探讨巴西蜂胶乙醇提取物(EEBP)对两种主要存活信号ERK1/2 和 Akt 的影响,并阐明这些信号的变化是否实际上参与了蜂胶的抗血管生成作用。Western blot 检测显示,EEBP 抑制 ERK1/2 的磷酸化,但不抑制 Akt 的磷酸化。U0126 的药理学抑制作用表明,ERK1/2 的失活足以抑制管腔形成并诱导细胞凋亡。研究还表明,EEBP 和 U0126 同样诱导 caspase-3 的激活和多聚 ADP-核糖聚合酶(PARP)和层粘连蛋白 A/C 的裂解,这些都是细胞凋亡的分子标志物。这些结果表明,抑制存活信号 ERK1/2 并随后诱导细胞凋亡是 EEBP 抑制血管生成的关键机制。