PUBLICATION
Low doses of ionizing radiation promote tumor growth and metastasis by enhancing angiogenesis
- Authors
- Sofia Vala, I., Martins, L.R., Imaizumi, N., Nunes, R.J., Rino, J., Kuonen, F., Carvalho, L.M., Rüegg, C., Grillo, I.M., Barata, J.T., Mareel, M., and Santos, S.C.
- ID
- ZDB-PUB-100625-30
- Date
- 2010
- Source
- PLoS One 5(6): e11222 (Journal)
- Registered Authors
- Keywords
- Endothelial cells, Angiogenesis, Zebrafish, Apoptosis, Radiation therapy, Metastasis, Cell migration, Lung and intrathoracic tumors
- MeSH Terms
-
- Animals
- Antibodies, Monoclonal/pharmacology
- Antibodies, Monoclonal, Humanized
- Apoptosis/drug effects
- Apoptosis/radiation effects
- Bevacizumab
- Cell Hypoxia
- Cell Line, Tumor
- Cell Movement/radiation effects
- Collagen/metabolism
- Dose-Response Relationship, Radiation
- Drug Combinations
- Endothelial Cells/pathology
- Endothelial Cells/radiation effects
- Gene Expression Regulation, Neoplastic/radiation effects
- Humans
- Laminin/metabolism
- MAP Kinase Signaling System/radiation effects
- Mice
- Microvessels/drug effects
- Microvessels/metabolism
- Microvessels/radiation effects
- Neoplasm Metastasis/pathology*
- Neoplasms/blood supply*
- Neoplasms/genetics
- Neoplasms/pathology*
- Neoplasms/radiotherapy
- Neovascularization, Pathologic/pathology*
- Phosphatidylinositol 3-Kinases/metabolism
- Proteoglycans/metabolism
- Proto-Oncogene Proteins c-akt/metabolism
- Radiotherapy Dosage
- Regeneration/radiation effects
- Vascular Endothelial Growth Factor A/metabolism
- Vascular Endothelial Growth Factor Receptor-2/metabolism
- Zebrafish/embryology
- Zebrafish/physiology
- PubMed
- 20574535 Full text @ PLoS One
Citation
Sofia Vala, I., Martins, L.R., Imaizumi, N., Nunes, R.J., Rino, J., Kuonen, F., Carvalho, L.M., Rüegg, C., Grillo, I.M., Barata, J.T., Mareel, M., and Santos, S.C. (2010) Low doses of ionizing radiation promote tumor growth and metastasis by enhancing angiogenesis. PLoS One. 5(6):e11222.
Abstract
Radiotherapy is a widely used treatment option in cancer. However, recent evidence suggests that doses of ionizing radiation (IR) delivered inside the tumor target volume, during fractionated radiotherapy, can promote tumor invasion and metastasis. Furthermore, the tissues that surround the tumor area are also exposed to low doses of IR that are lower than those delivered inside the tumor mass, because external radiotherapy is delivered to the tumor through multiple radiation beams, in order to prevent damage of organs at risk. The biological effects of these low doses of IR on the healthy tissue surrounding the tumor area, and in particular on the vasculature remain largely to be determined. We found that doses of IR lower or equal to 0.8 Gy enhance endothelial cell migration without impinging on cell proliferation or survival. Moreover, we show that low-dose IR induces a rapid phosphorylation of several endothelial cell proteins, including the Vascular Endothelial Growth Factor (VEGF) Receptor-2 and induces VEGF production in hypoxia mimicking conditions. By activating the VEGF Receptor-2, low-dose IR enhances endothelial cell migration and prevents endothelial cell death promoted by an anti-angiogenic drug, bevacizumab. In addition, we observed that low-dose IR accelerates embryonic angiogenic sprouting during zebrafish development and promotes adult angiogenesis during zebrafish fin regeneration and in the murine Matrigel assay. Using murine experimental models of leukemia and orthotopic breast cancer, we show that low-dose IR promotes tumor growth and metastasis and that these effects were prevented by the administration of a VEGF receptor-tyrosine kinase inhibitor immediately before IR exposure. These findings demonstrate a new mechanism to the understanding of the potential pro-metastatic effect of IR and may provide a new rationale basis to the improvement of current radiotherapy protocols.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping