Kim Mun-Hyeon, Jeong Yun-Jeong, Cho Hyun-Ji, Hoe Hyang-Sook, Park Kwan-Kyu, Park Yoon-Yub, Choi Yung Hyun, Kim Cheorl-Ho, Chang Hyeun-Wook, Park Young-Ja, Chung Il-Kyung, Chang Young-Chae
Research Institute of Biomedical Engineering and Department of Medicine, Catholic University of Daegu School of Medicine, Daegu 705-718, Republic of Korea.
Department of Neural Development and Disease, Korea Brain Research Institute (KBRI), Daegu 701-300, Republic of Korea.
Oncol Rep. 2017 Feb;37(2):777-784. doi: 10.3892/or.2016.5296. Epub 2016 Dec 7.
Delphinidin, a polyphenol that belongs to the group of anthocyanidins and is abundant in many pigmented fruits and vegetables, possesses important antioxidant, anti‑inflammatory, anti-mutagenic and anticancer properties. In the present study, we investigated the inhibitory effects of delphinidin on vascular endothelial growth factor (VEGF) expression, an important factor involved in angiogenesis and tumor progression, in A549 human lung cancer cells. Delphinidin inhibited CoCl2- and epidermal growth factor (EGF)-induced VEGF mRNA expression and VEGF protein production. Delphinidin also decreased CoCl2- and EGF-stimulated expression of hypoxia‑inducible factor (HIF)‑1α, which is a transcription factor of VEGF. Delphinidin suppressed CoCl2- and EGF-induced hypoxia‑response element (HRE) promoter activity, suggesting that the inhibitory effects of delphinidin on VEGF expression are caused by the suppression of the binding of HIF-1 to the HRE promoter. We also found that delphinidin specifically decreased the CoCl2- and EGF-induced HIF-1α protein expression by blocking the ERK and PI3K/Akt/mTOR/p70S6K signaling pathways, whereas the p38-mediated pathways were not involved. In animal models, EGF-induced new blood vessel formation was significantly inhibited by delphinidin. Therefore, our results indicate that delphinidin has a potentially new role in anti‑angiogenic action by inhibiting HIF-1α and VEGF expression.
飞燕草素是一种属于花青素类的多酚,在许多有色水果和蔬菜中含量丰富,具有重要的抗氧化、抗炎、抗诱变和抗癌特性。在本研究中,我们研究了飞燕草素对A549人肺癌细胞中血管内皮生长因子(VEGF)表达的抑制作用,VEGF是参与血管生成和肿瘤进展的一个重要因子。飞燕草素抑制了氯化钴(CoCl₂)和表皮生长因子(EGF)诱导的VEGF mRNA表达以及VEGF蛋白生成。飞燕草素还降低了CoCl₂和EGF刺激的缺氧诱导因子(HIF)-1α的表达,HIF-1α是VEGF的转录因子。飞燕草素抑制了CoCl₂和EGF诱导的缺氧反应元件(HRE)启动子活性,这表明飞燕草素对VEGF表达的抑制作用是由抑制HIF-1与HRE启动子的结合引起的。我们还发现,飞燕草素通过阻断ERK和PI3K/Akt/mTOR/p70S6K信号通路特异性地降低了CoCl₂和EGF诱导下的HIF-1α蛋白表达,而p38介导的信号通路未参与其中。在动物模型中,飞燕草素显著抑制了EGF诱导的新血管形成。因此,我们的结果表明,飞燕草素通过抑制HIF-1α和VEGF表达在抗血管生成作用中具有潜在的新作用。