Abstract:
:Tumor angiogenesis is a critical step for the growth and metastasis of solid tumors. Vascular endothelial growth factor (VEGF) is the most important angiogenic molecule associated with tumor-induced neovascularization. VEGF exerts its activity through binding to its receptor tyrosine kinase, KDR/Flk-1, expressed on the surface of endothelial cells. From the screening of medicinal plants, we have identified 1,2,3,4,6-penta-O-galloyl-beta-d-glucose (PGG) from the roots of Paeonia lactiflora that inhibited the binding of VEGF to KDR/Flk-1. PGG efficiently blocked VEGF-induced human umbilical vein endothelial cell proliferation and the growth of immortalized human microvascular endothelial cells, but did not affect the growth of HT1080 human fibrosarcoma and DU-145 human prostate carcinoma cells. PGG also blocked VEGF-induced capillary-like tube formation of endothelial cell on Matrigel. Our results suggest that PGG could be a candidate for developing anti-angiogenic agent.
journal_name
Cancer Lettjournal_title
Cancer lettersauthors
Lee SJ,Lee HM,Ji ST,Lee SR,Mar W,Gho YSdoi
10.1016/j.canlet.2003.11.008keywords:
subject
Has Abstractpub_date
2004-05-10 00:00:00pages
89-94issue
1eissn
0304-3835issn
1872-7980pii
S0304383503007821journal_volume
208pub_type
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