Carbon ion beam is more effective to induce cell death in sphere-type A172 human glioblastoma cells compared with X-rays

Int J Radiat Biol. 2014 Dec;90(12):1125-32. doi: 10.3109/09553002.2014.927933. Epub 2014 Aug 11.

Abstract

Purpose: To obtain human glioblastoma cells A172 expressing stem cell-related protein and comparison of radiosensitivity in these cells with X-rays and carbon beam.

Methods: Human monolayer-type A172 glioblastoma cells were maintained in normal medium with 10% bovine serum. In order to obtain sphere-type A172 cells the medium was replaced with serum-free medium supplemented with growth factors. Both types of A172 cells were irradiated with either X-rays or carbon ion beams and their radiosensitivity was evaluated.

Results: Serum-free medium induced expression of stem cell-related proteins in A172 cells along with the neurosphere-like appearance. These sphere-type cells were found resistant to both X-rays and carbon ion beams. Phosphorylation of histone H2A family member X persisted for a longer period in the cells exposed to carbon ion beams than in those exposed to X-rays and it disappeared quicker in the sphere type than in the monolayer type. Relative radioresistance of the sphere type cells was smaller for carbon ion beams than for X-rays.

Conclusions: We demonstrated that glioblastoma A172 cells with induced stem cell-related proteins turned resistant to irradiation. Accelerated heavy ion particles may have advantage over X-rays in overcoming the tumor resistance due to cell stemness.

Keywords: Glioblastoma cells; radiosensitivity; stem cells.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbon / pharmacology*
  • Cell Death / drug effects
  • Cell Death / radiation effects
  • Cell Line, Tumor
  • DNA / biosynthesis
  • DNA / genetics
  • DNA Breaks, Double-Stranded / drug effects
  • DNA Breaks, Double-Stranded / radiation effects
  • Endothelial Growth Factors / pharmacology
  • Fibroblast Growth Factors / pharmacology
  • Gene Expression Regulation, Neoplastic / drug effects
  • Gene Expression Regulation, Neoplastic / radiation effects
  • Glioblastoma / pathology*
  • Heavy Ion Radiotherapy*
  • Humans
  • Neoplastic Stem Cells / drug effects
  • Neoplastic Stem Cells / metabolism
  • Neoplastic Stem Cells / pathology
  • Neoplastic Stem Cells / radiation effects
  • Radiation Tolerance / drug effects
  • Radiation Tolerance / radiation effects
  • X-Ray Therapy*

Substances

  • Endothelial Growth Factors
  • Fibroblast Growth Factors
  • Carbon
  • DNA