Norepinephrine induces VEGF expression and angiogenesis by a hypoxia-inducible factor-1 alpha protein-dependent mechanism

作者：Park Soon Young; Kang Joo Hee; Jeong Kang Jin; Lee Jangsoon; Han Jeong Whan; Choi Wahn Soo; Kim Yong Kee; Kang Jaeku; Park Chang Gyo; Lee Hoi Young^*

来源：International Journal of Cancer, 2011, 128(10): 2306-2316.

DOI：10.1002/ijc.25589

• norepinephrine
• angiogenesis
• vascular endothelial growth factor
• hypoxia-inducible factor
• adrenergic receptors

A growing number of studies have demonstrated that physiological factors can influence the progression of several cancers via cellular immune function, angiogenesis and metastasis. Recently, stress-induced catecholamines have been shown to increase the expression of various cancer progressive factors, including vascular endothelial growth factor (VEGF), matrix metalloproteinases and interleukins. However, a detailed mechanism remains to be identified. In this study, we investigated the role of adrenergic receptors and hypoxia-inducible factor (HIF)-1 alpha protein in catecholamine-induced VEGF expression and angiogenesis. Treatment of the cells with norepinephrine (NE) or isoproterenol induced VEGF expression and HIF-1 alpha protein amount in a dose-dependent manner. Induction of VEGF expression by NE was abrogated when the cells were transfected with HIF-1 alpha-specific siRNA. Similarly, adenylate cyclase activator forskolin and cyclic AMP-dependent protein kinase A inhibitor H-89 enhanced and decreased HIF-1 alpha protein amount, respectively. More importantly, conditioned medium of NE-stimulated cancer cells induced angiogenesis in a HIF-1 alpha protein-dependent manner. In addition, pretreatment of cells with propranolol, a beta-adrenergic receptor (AR) blocker, completely abolished induction of VEGF expression and HIF-1 alpha protein amount by NE in all of the tested cancer cells. However, treatment with the alpha 1-AR blocker prazosin inhibited NE-induced HIF-1 alpha protein amount and angiogenesis in SK-Hep1 and PC-3 but not MDA-MB-231 cells. Collectively, our results suggest that ARs and HIF-1 alpha protein have critical roles in NE-induced VEGF expression in cancer cells, leading to stimulation of angiogenesis. These findings will help to understand the mechanism of cancer progression by stress-induced catecholamines and design therapeutic strategies for cancer angiogenesis.

• 出版日期2011-5-1