Mikhail Dikov
Faculty Member

The Foxc2 transcription factor regulates tumor angiogenesis.

Sano H, Leboeuf JP, Novitskiy SV, Seo S, Zaja-Milatovic S, Dikov MM, Kume T
Biochem Biophys Res Commun. 2010 392 (2): 201-6

PMID: 20060810 · PMCID: PMC2822046 · DOI:10.1016/j.bbrc.2010.01.015

The Forkhead/Fox transcription factor Foxc2 is a critical regulator of vascular development. However, the role of Foxc2 in pathological angiogenesis in cancer remains unknown. Here we show that FoxC2 is highly expressed in human breast and colonic tumors and in the tumor endothelium in human and mouse melanomas. Using the B16 melanoma tumor model, we investigated the function of Foxc2 in tumor angiogenesis. After subcutaneous injection of B16 melanoma cells, primary tumor growth as well as neovascularization was markedly reduced in mice lacking one copy of the Foxc2 gene (Foxc2+/-). Consistently, expression levels of several angiogenic factors, including vascular endothelial growth factor (Vegf), matrix metallopeptidase 2 (Mmp2), and platelet-derived growth factor-B (Pdgfb), were significantly decreased in B16 tumors grown in Foxc2+/- mice, and tumor blood vessels formed in Foxc2+/- mice showed reduced coverage of mural cells and endothelial cell apoptosis. In addition, the tumor tissue in Foxc2+/- mice had an accumulation of necrotic cells. Taken together, these findings demonstrate that haplodeficiency of Foxc2 results in impaired formation of tumor blood vessels as well as reduced tumor growth and thereby provide evidence that Foxc2 is critical for tumor development and angiogenesis.

2010 Elsevier Inc. All rights reserved.

MeSH Terms (15)

Animals Apoptosis Cell Line, Tumor Endothelium, Vascular Forkhead Transcription Factors Gene Flow Heterozygote Humans Matrix Metalloproteinase 2 Melanoma, Experimental Mice Mice, Mutant Strains Neoplasms Neovascularization, Pathologic Vascular Endothelial Growth Factor A

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