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Delphinidin inhibits angiogenesis through the suppression of HIF-1α and VEGF expression in A549 lung cancer cells

Authors :
Hyeun-Wook Chang
Yoon-Yub Park
Kwan-Kyu Park
Mun-Hyeon Kim
Cheorl-Ho Kim
Il-Kyung Chung
Hyun-Ji Cho
Yun-Jeong Jeong
Hyang-Sook Hoe
Young-Ja Park
Yung Hyun Choi
Young-Chae Chang
Source :
Oncology Reports. 37:777-784
Publication Year :
2016
Publisher :
Spandidos Publications, 2016.

Abstract

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.

Details

ISSN :
17912431 and 1021335X
Volume :
37
Database :
OpenAIRE
Journal :
Oncology Reports
Accession number :
edsair.doi.dedup.....48461fc0f7a35332d9076d69a731ef15
Full Text :
https://doi.org/10.3892/or.2016.5296