Marine Drugs | |
Low Molecular Weight Fucoidan Inhibits Tumor Angiogenesis through Downregulation of HIF-1/VEGF Signaling under Hypoxia | |
Meng-Chuan Chen2  Wen-Lin Hsu3  Pai-An Hwang1  Tz-Chong Chou2  | |
[1] Seafood Technology Division, Fisheries Research Institute, Council of Agriculture, Keelung 20246, Taiwan; E-Mail:;Graduate Institute of Medical Sciences, National Defense Medical Center, Taipei 11483, Taiwan; E-Mail:;School of Medicine, Tzu Chi University, Hualien 97002, Taiwan; E-Mail: | |
关键词: low molecular weight fucoidan; angiogenesis; hypoxia-inducible factor 1 alpha; vascular endothelial growth factor; bladder cancer; | |
DOI : 10.3390/md13074436 | |
来源: mdpi | |
【 摘 要 】
Activation of hypoxia-induced hypoxia-inducible factors-1 (HIF-1) plays a critical role in promoting tumor angiogenesis, growth and metastasis. Low molecular weight fucoidan (LMWF) is prepared from brown algae, and exhibits anticancer activity. However, whether LMWF attenuates hypoxia-induced angiogenesis in bladder cancer cells and the molecular mechanisms involved remain unclear. This is the first study to demonstrate that LMWF can inhibit hypoxia-stimulated H2O2 formation, HIF-1 accumulation and transcriptional activity vascular endothelial growth factor (VEGF) secretion, and the migration and invasion in hypoxic human bladder cancer cells (T24) cells. LMWF also downregulated hypoxia-activated phosphorylation of PI3K/AKT/mTOR/p70S6K/4EBP-1 signaling in T24 cells. Blocking PI3K/AKT or mTOR activity strongly diminished hypoxia-induced HIF-1α expression and VEGF secretion in T24 cells, supporting the involvement of PI3K/AKT/mTOR in the induction of HIF-1α and VEGF. Additionally, LMWF significantly attenuated angiogenesis
【 授权许可】
CC BY
© 2015 by the authors; licensee MDPI, Basel, Switzerland.
【 预 览 】
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