Radiation-induced motility alterations in medulloblastoma cells

J Radiat Res. 2015 May;56(3):430-6. doi: 10.1093/jrr/rru120. Epub 2015 Mar 2.

Abstract

Photon irradiation has been repeatedly suspected of increasing tumor cell motility and promoting locoregional recurrence of disease. This study was set up to analyse possible mechanisms underlying the potentially radiation-altered motility in medulloblastoma cells. Medulloblastoma cell lines D425 and Med8A were analyzed in migration and adhesion experiments with and without photon and carbon ion irradiation. Expression of integrins was determined by quantitative FACS analysis. Matrix metalloproteinase concentrations within cell culture supernatants were investigated by enzyme-linked immunosorbent assay (ELISA). Statistical analysis was performed using Student's t-test. Both photon and carbon ion irradiation significantly reduced chemotactic medulloblastoma cell transmigration through 8-μm pore size membranes, while simultaneously increasing adherence to fibronectin- and collagen I- and IV-coated surfaces. Correspondingly, both photon and carbon ion irradiation downregulate soluble MMP9 concentrations, while upregulating cell surface expression of proadhesive extracellular matrix protein-binding integrin α5. The observed phenotype of radiation-altered motility is more pronounced following carbon ion than photon irradiation. Both photon and (even more so) carbon ion irradiation are effective in inhibiting medulloblastoma cell migration through downregulation of matrix metalloproteinase 9 and upregulation of proadhesive cell surface integrin α5, which lead to increased cell adherence to extracellular matrix proteins.

Keywords: adhesion; integrin; matrix metalloproteinase; medulloblastoma; migration; particle radiotherapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbon
  • Cell Adhesion / radiation effects*
  • Cell Adhesion Molecules / metabolism
  • Cell Line, Tumor
  • Cell Movement / radiation effects*
  • Dose-Response Relationship, Radiation
  • Extracellular Matrix Proteins / metabolism
  • Heavy Ions*
  • Humans
  • Matrix Metalloproteinase 9 / metabolism*
  • Medulloblastoma / pathology
  • Medulloblastoma / physiopathology*
  • Photons
  • Radiation Dosage
  • Receptors, Vitronectin / metabolism*

Substances

  • Cell Adhesion Molecules
  • Extracellular Matrix Proteins
  • Receptors, Vitronectin
  • integrin alphaVbeta5
  • Carbon
  • MMP9 protein, human
  • Matrix Metalloproteinase 9