Ligustrazine inhibits B16F10 melanoma metastasis and suppresses angiogenesis induced by Vascular Endothelial Growth Factor

Angiogenesis is crucial for tumor metastasis, with many compounds that inhibit tumor metastasis acting through suppression of angiogenesis. We investigated anti-angiogenic properties of Ligustrazine in a series of in vitro and in vivo models. Ligustrazine inhibited VEGF-induced HUVECs migration and...

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Published inBiochemical and biophysical research communications Vol. 386; no. 2; pp. 374 - 379
Main Authors Chen, Lei, Lu, Yin, Wu, Jia-ming, Xu, Bo, Zhang, Li-juan, Gao, Ming, Zheng, Shi-zhong, Wang, Ai-yun, Zhang, Chang-bin, Zhang, Wei-wei, Lei, Na
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 21.08.2009
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Summary:Angiogenesis is crucial for tumor metastasis, with many compounds that inhibit tumor metastasis acting through suppression of angiogenesis. We investigated anti-angiogenic properties of Ligustrazine in a series of in vitro and in vivo models. Ligustrazine inhibited VEGF-induced HUVECs migration and tube formation in a dose-dependent manner in vitro, and had limited cytotoxicity to HUVECs and normal fibroblasts even at a dose up to 100 μg/ml. Ligustrazine also suppressed VEGF-induced rat aortic ring sprouting dose-dependently. In vivo, Ligustrazine reduced the Hb content in a Matrigel plug implanted in mice and inhibited new vessel formation in CAM. In addition, in a B16F10 spontaneous metastasis model, Ligustrazine decreased the expression of CD34 and VEGF in primary tumor tissue and reduced the number of metastasis nodi on the lung surface. Our data suggests that Ligustrazine may inhibit tumor metastasis, at least in part, through its anti-angiogenic activity.
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ISSN:0006-291X
1090-2104
1090-2104
DOI:10.1016/j.bbrc.2009.06.042