Carbon ion irradiation inhibits glioma cell migration through downregulation of integrin expression

Int J Radiat Oncol Biol Phys. 2012 May 1;83(1):394-9. doi: 10.1016/j.ijrobp.2011.06.2004. Epub 2011 Nov 4.

Abstract

Purpose: To investigate the effect of carbon ion irradiation on glioma cell migration.

Methods and materials: U87 and Ln229 glioma cells were irradiated with photons and carbon ions. Migration was analyzed 24 h after irradiation. Fluorescence-activated cell sorting analysis was performed in order to quantify surface expression of integrins.

Results: Single photon doses of 2 Gy and 10 Gy enhanced α(ν)β(3) and α(ν)β(5) integrin expression and caused tumor cell hypermigration on both vitronectin (Vn) and fibronectin (Fn). Compared to integrin expression in unirradiated cells, carbon ion irradiation caused decreased integrin expression and inhibited cell migration on both Vn and Fn.

Conclusion: Photon radiotherapy (RT) enhances the risk of tumor cell migration and subsequently promotes locoregional spread via photon induction of integrin expression. In contrast to photon RT, carbon ion RT causes decreased integrin expression and suppresses glioma cell migration on both Vn and Fn, thus promising improved local control.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbon / therapeutic use*
  • Cell Line, Tumor
  • Cell Movement / physiology
  • Cell Movement / radiation effects*
  • Down-Regulation / physiology
  • Down-Regulation / radiation effects*
  • Fibronectins / physiology
  • Glioma / metabolism
  • Glioma / pathology
  • Glioma / radiotherapy*
  • Humans
  • Integrin alphaVbeta3 / metabolism
  • Integrin alphaVbeta3 / radiation effects*
  • Neoplasm Proteins / metabolism
  • Neoplasm Proteins / radiation effects*
  • Photons / adverse effects
  • Photons / therapeutic use
  • Radiation Dosage
  • Receptors, Vitronectin / metabolism
  • Receptors, Vitronectin / radiation effects*
  • Vitronectin / physiology

Substances

  • Fibronectins
  • Integrin alphaVbeta3
  • Neoplasm Proteins
  • Receptors, Vitronectin
  • Vitronectin
  • integrin alphaVbeta5
  • Carbon