Journal
MOLECULAR CANCER THERAPEUTICS
Volume 8, Issue 9, Pages 2645-2654Publisher
AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1535-7163.MCT-09-0383
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Funding
- SENTER/NOVEM
- Belgian American Educational Foundation
- Centre Anticancereux
- Fonds National de la Recherche Scientifique
- Region Wallonne
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In tumor cells, the transcription factor NF-kappa B has been described to be antiapoptotic and proproliferative and involved in the production of angiogenic factors such as vascular endothelial growth factor. From these data, a protumorigenic role of NF-kappa B has emerged. Here, we examined in endothelial cells whether NF-kappa B signaling pathway is involved in mediating the angiostatic properties of angiogenesis inhibitors. The current report describes that biochemically unrelated agents with direct angiostatic effect induced NF-kappa B activation in endothelial cells. Our data showed that endostatin, anginex, angiostatin, and the 16-kDa N-terminal fragment of human prolactin induced NF-kappa B activation in endothelial cells in both cultured human endothelial cells and in vivo in a mouse tumor model. It was also found that NF-kappa B activity was required for the angiostatic activity, because inhibition of NF-kappa B in endothelial cells impaired the ability of angiostatic agents to block sprouting of endothelial cells and to overcome endothelial cell anergy. Therefore, activation of NF-kappa B in endothelial cells can result in an unexpected antitumor outcome. Based on these data, the current approach of systemic treatment with NF-kappa B inhibitors may therefore be revisited because NF-kappa B activation specifically targeted to endothelial cells might represent an efficient strategy for the treatment of cancer. [Mol Cancer Ther 2009;8(9):2645-54]
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