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http://dx.doi.org/10.5657/FAS.2014.0305

Dieckol Suppresses CoCl2-induced Angiogenesis in Endothelial Cells  

Jung, Seung Hyun (Department of Chemistry, Pukyong National University)
Jang, In Seung (Department of Chemistry, Pukyong National University)
Jeon, You-Jin (Department of Marine Life Science, Jeju National University)
Kim, Young-Mog (Department of Food Science & Technology, Pukyong National University)
Park, Sun Joo (Department of Chemistry, Pukyong National University)
Publication Information
Fisheries and Aquatic Sciences / v.17, no.3, 2014 , pp. 305-311 More about this Journal
Abstract
Dieckol is a polyphenol compound isolated from brown algae that has anti-oxidant, anti-inflammatory, and anti-tumor activity. We examined the anti-angiogenic effects of dieckol in endothelial cells under hypoxic conditions. Treatment with $CoCl_2$, a hypoxic mimetic agent, increased proliferation, adhesion, migration, and tube formation in HUVECs, as well as vessel sprouting in rat aortic rings, which correlated well with increased expression of hypoxia-inducible factor 1-alpha ($HIF1{\alpha}$) and ${\beta}1$-integrin. Dieckol suppressed $CoCl_2$-induced adhesion, migration, and tube formation in HUVECs and vessel sprouting in rat aortic rings. Dieckol treatment decreased $CoCl_2$-induced overexpression of $HIF1{\alpha}$ and its downstream signaling molecules, including ${\beta}1$-integrin/Fak, Akt/eNOS, and p38 MAPK. These results suggest that dieckol is a novel angiogenesis inhibitor and a potential treatment for angiogenesis-dependent diseases in humans, such as malignant tumors.
Keywords
Dieckol; Angiogenesis; $HIF1{\alpha}$; ${\beta}1$-integrin;
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