IDH1(R132H) mutation causes a less aggressive phenotype and radiosensitizes human malignant glioma cells independent of the oxygenation status

Radiother Oncol. 2015 Sep;116(3):381-7. doi: 10.1016/j.radonc.2015.08.007. Epub 2015 Aug 29.

Abstract

Background and purpose: In malignant glioma the presence of the IDH1 mutation (IDH1(R132H)) is associated with better clinical outcome. However, it is unclear whether IDH1 mutation is associated with a less aggressive phenotype or directly linked to increased sensitivity to radiotherapy.

Material and methods: We determined the influence of IDH1(R132H) mutant protein on proliferation and growth in 3D culture, migration, cell survival and radiosensitivity in vitro under normoxia (21% O2) and hypoxia (<1% O2) in a panel of human malignant glioma cell lines (U-251MG, U-343MG, LN-229) with stable overexpression of wild-type (IDH1(wt)) and mutated IDH1 (IDH1(R132H)).

Results: Overexpression of IDH1(R132H) in glioma cells resulted in slightly decreased cell proliferation, considerably reduced cell migration and caused differences in growth properties in 3D spheroid cultures. Furthermore, IDH1(R132H)-positive cells consistently demonstrated an increased radiosensitivity in human malignant glioma cells U-251MG (DMF10: 1.52, p<0.01 and 1.42, p<0.01), U-343MG (DMF10: 1.78, p<0.01 and 1.75, p<0.01) and LN-229 (DMF10: 1.41, p<0.05 and 1.68, p<0.01) under normoxia and hypoxia, respectively.

Conclusion: Our data indicate that IDH1(R132H) mutation causes both a less aggressive biological behavior and direct radiosensitization of human malignant glioma cells. Targeting IDH1 appears to be an attractive approach in combination with radiotherapy.

Keywords: Glioma; Hypoxia; IDH1; IDH1(R132H); Isocitrate dehydrogenase 1; Radiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Proliferation
  • Cell Survival / genetics
  • Glioma / genetics
  • Glioma / radiotherapy*
  • Humans
  • Hypoxia / genetics*
  • Hypoxia / physiopathology
  • Isocitrate Dehydrogenase / genetics
  • Isocitrate Dehydrogenase / pharmacology*
  • Mutation / genetics*
  • Mutation / physiology
  • Phenotype
  • Radiation Tolerance / genetics*
  • Radiation Tolerance / physiology
  • Radiation-Sensitizing Agents / pharmacology*

Substances

  • Radiation-Sensitizing Agents
  • Isocitrate Dehydrogenase
  • IDH1 protein, human