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Marine bromophenol bis(2,3,6-tribromo-4, 5-dihydroxybenzyl)ether inhibits angiogenesis in human umbilical vein endothelial cells and reduces vasculogenic mimicry in human lung cancer a549 cells

Thumbnail
Autor
Dong S., Chen Z., Wang L., Liu Y., Stagos D., Lin X., Liu M.
Fecha
2021
Language
en
DOI
10.3390/md19110641
Materia
bis(2,3,6 tribromo 4,5 dihydroxybenzyl)ether
gelatinase B
phenol
unclassified drug
angiogenesis inhibitor
phenol derivative
A-549 cell line
angiogenesis
animal experiment
antiangiogenic activity
Article
cell invasion
cell migration
cell plasticity
controlled study
drug structure
embryo
human
human cell
in vitro study
in vivo study
nonhuman
tubulogenesis
umbilical vein endothelial cell
vasculogenic mimicry
zebra fish
A-549 cell line
angiogenesis
animal
aquatic species
cell proliferation
chemistry
drug effect
microalga
umbilical vein endothelial cell
A549 Cells
Angiogenesis Inhibitors
Animals
Aquatic Organisms
Cell Proliferation
Human Umbilical Vein Endothelial Cells
Humans
Microalgae
Neovascularization, Physiologic
Phenols
MDPI
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Resumen
Angiogenesis, including the growth of new capillary blood vessels from existing ones and the malignant tumors cells formed vasculogenic mimicry, is quite important for the tumor metastasis. Anti-angiogenesis is one of the significant therapies in tumor treatment, while the clinical angiogenesis inhibitors usually exhibit endothelial cells dysfunction and drug resistance. Bis(2,3,6tribromo-4,5-dihydroxybenzyl)ether (BTDE), a marine algae-derived bromophenol compound, has shown various biological activities, however, its anti-angiogenesis function remains unknown. The present study illustrated that BTDE had anti-angiogenesis effect in vitro through inhibiting human umbilical vein endothelial cells migration, invasion, tube formation, and the activity of matrix metalloproteinases 9 (MMP9), and in vivo BTDE also blocked intersegmental vessel formation in zebrafish embryos. Moreover, BTDE inhibited the migration, invasion, and vasculogenic mimicry formation of lung cancer cell A549. All these results indicated that BTDE could be used as a potential candidate in anti-angiogenesis for the treatment of cancer. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
URI
http://hdl.handle.net/11615/73417
Colecciones
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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