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Mol Oncol. 2007 Dec;1(3):288-302. doi: 10.1016/j.molonc.2007.10.003.

Vascular endothelial growth factor restores delayed tumor progression in tumors depleted of macrophages.

Author information

1
Department of Developmental and Molecular Biology, Center of Reproductive Biology and Women's Health, Albert Einstein Cancer Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA

Abstract

Genetic depletion of macrophages in Polyoma Middle T oncoprotein (PyMT)-induced mammary tumors in mice delayed the angiogenic switch and the progression to malignancy. To determine whether vascular endothelial growth factor A (VEGF-A) produced by tumor-associated macrophages regulated the onset of the angiogenic switch, a genetic approach was used to restore expression of VEGF-A into tumors at the benign stages. This stimulated formation of a high-density vessel network and in macrophage-depleted mice, was followed by accelerated tumor progression. The expression of VEGF-A led to a massive infiltration into the tumor of leukocytes that were mostly macrophages. This study suggests that macrophage-produced VEGF regulates malignant progression through stimulating tumor angiogenesis, leukocytic infiltration and tumor cell invasion.

KEYWORDS:

PyMT; VEGF; angiogenesis; macrophages; malignancy; mammary; mouse; progression; transgenic; tumor

PMID:
18509509
PMCID:
PMC2396497
DOI:
10.1016/j.molonc.2007.10.003
[Indexed for MEDLINE]
Free PMC Article

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