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Cancers (Basel). 2015 Mar 18;7(1):481-502. doi: 10.3390/cancers7010481.

Effects of Alpha Particle and Proton Beam Irradiation as Putative Cross-Talk between A549 Cancer Cells and the Endothelial Cells in a Co-Culture System.

Cancers

Hélène Riquier, Denis Abel, Anne-Catherine Wera, Anne-Catherine Heuskin, Géraldine Genard, Stéphane Lucas, Carine Michiels

Affiliations

  1. URBC-NARILIS, University of Namur, 61 rue de Bruxelles, Namur 5000, Belgium. [email protected].
  2. URBC-NARILIS, University of Namur, 61 rue de Bruxelles, Namur 5000, Belgium. [email protected].
  3. LARN-PMR, NARILIS, University of Namur, Namur 5000, Belgium. [email protected].
  4. LARN-PMR, NARILIS, University of Namur, Namur 5000, Belgium. [email protected].
  5. URBC-NARILIS, University of Namur, 61 rue de Bruxelles, Namur 5000, Belgium. [email protected].
  6. LARN-PMR, NARILIS, University of Namur, Namur 5000, Belgium. [email protected].
  7. URBC-NARILIS, University of Namur, 61 rue de Bruxelles, Namur 5000, Belgium. [email protected].

PMID: 25794049 PMCID: PMC4381270 DOI: 10.3390/cancers7010481

Abstract

BACKGROUND: High-LET ion irradiation is being more and more often used to control tumors in patients. Given that tumors are now considered as complex organs composed of multiple cell types that can influence radiosensitivity, we investigated the effects of proton and alpha particle irradiation on the possible radioprotective cross-talk between cancer and endothelial cells.

MATERIALS AND METHODS: We designed new irradiation chambers that allow co-culture study of cells irradiated with a particle beam. A549 lung carcinoma cells and endothelial cells (EC) were exposed to 1.5 Gy of proton beam or 1 and 2 Gy of alpha particles. Cell responses were studied by clonogenic assays and cell cycle was analyzed by flow cytometry. Gene expression studies were performed using Taqman low density array and by RT-qPCR.

RESULTS: A549 cells and EC displayed similar survival fraction and they had similar cell cycle distribution when irradiated alone or in co-culture. Both types of irradiation induced the overexpression of genes involved in cell growth, inflammation and angiogenesis.

CONCLUSIONS: We set up new irradiation chamber in which two cell types were irradiated together with a particle beam. We could not show that tumor cells and endothelial cells were able to protect each other from particle irradiation. Gene expression changes were observed after particle irradiation that could suggest a possible radioprotective inter-cellular communication between the two cell types but further investigations are needed to confirm these results.

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