Inorganic phosphate induces cancer cell mediated angiogenesis dependent on forkhead box protein C2 (FOXC2) regulated osteopontin expression

Recent studies in both rodents and humans suggest that elevated serum phosphorus, in the context of normal renal function, potentiates, or exacerbates pathologies associates with cardiovascular disease, bone metabolism, and cancer. Our recent microarray studies identified the potent stimulation of p...

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Bibliographic Details
Published in:Molecular carcinogenesis 2015-09, Vol.54 (9), p.926-934
Main Authors: Lin, Yiming, McKinnon, Kelly E., Ha, Shin Woo, Beck Jr, George R.
Format: Article
Language:English
Subjects:
Angiogenesis
Breast - blood supply
Breast - metabolism
Breast Neoplasms - blood supply
Breast Neoplasms - genetics
Breast Neoplasms - metabolism
Cancer
Cell Line, Tumor
Cell Movement
Female
Forkhead Transcription Factors - genetics
Forkhead Transcription Factors - metabolism
FOXC2
Gene Expression Regulation, Neoplastic
Human Umbilical Vein Endothelial Cells
Humans
inorganic phosphate
Lung - blood supply
Lung - metabolism
Lung Neoplasms - blood supply
Lung Neoplasms - genetics
Lung Neoplasms - metabolism
migration
Neovascularization, Pathologic - genetics
Neovascularization, Pathologic - metabolism
osteopontin
Osteopontin - genetics
Osteopontin - metabolism
Phosphates
Phosphates - metabolism
Proteins
Tumor Microenvironment
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Summary:Recent studies in both rodents and humans suggest that elevated serum phosphorus, in the context of normal renal function, potentiates, or exacerbates pathologies associates with cardiovascular disease, bone metabolism, and cancer. Our recent microarray studies identified the potent stimulation of pro‐angiogenic genes such as forkhead box protein C2 (FOXC2), osteopontin, and Vegfα, among others in response to elevated inorganic phosphate (Pi). Increased angiogenesis and neovascularization are important events in tumor growth and the progression to malignancy and FOXC2 has recently been identified as a potential transcriptional regulator of these processes. In this study we addressed the possibility that a high Pi environment would increase the angiogenic potential of cancer cells through a mechanism requiring FOXC2. Our studies utilized lung and breast cancer cell lines in combination with the human umbilical vascular endothelial cell (HUVEC) vessel formation model to better understand the mechanism(s) by which a high Pi environment might alter cancer progression. Exposure of cancer cells to elevated Pi stimulated expression of FOXC2 and conditioned medium from the Pi‐stimulated cancer cells stimulated migration and tube formation in the HUVEC model. Mechanistically, we define the requirement of FOXC2 for Pi‐induced osteopontin (OPN) expression and secretion from cancer cells as necessary for the angiogenic response. These studies reveal for the first time that cancer cells grown in a high Pi environment promote migration of endothelial cells and tube formation and in so doing identify a novel potential therapeutic target to reduce tumor progression. © 2014 Wiley Periodicals, Inc.
ISSN:0899-1987
1098-2744
DOI:10.1002/mc.22153