In Vitro Methods for the Study of Glioblastoma Stem-Like Cell Radiosensitivity

Methods Mol Biol. 2021:2269:37-47. doi: 10.1007/978-1-0716-1225-5_3.

Abstract

Ionizing radiation is a critical component of glioblastoma (GBM) therapy. Recent data have implicated glioblastoma stem-like cells (GSCs) as determinants of GBM development, maintenance, and treatment response. Understanding the response of GSCs to radiation should thus provide insight into the development of improved GBM treatment strategies. Towards this end, in vitro techniques for the analysis of GSC radiosensitivity are an essential starting point. One such method, the clonogenic survival assay has been adapted to assessing the intrinsic radiosensitivity of GSCs and is described here. As an alternative method, the limiting dilution assay is presented for defining the radiosensitivity of GSC lines that do not form colonies or only grow as neurospheres. In addition to these cellular strategies, we describe γH2AX foci analysis, which provides a surrogate marker for radiosensitivity at the molecular level. Taken together, the in vitro methods presented here provide tools for defining intrinsic radiosensitivity of GSCs and for testing agents that may enhance GBM radioresponse.

Keywords: Clonogenic survival; Glioblastoma; In vitro radiosensitivity; Limiting dilution assay; γH2AX.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers, Tumor* / metabolism
  • Cell Line, Tumor
  • Genetic Loci*
  • Glioblastoma* / genetics
  • Glioblastoma* / metabolism
  • Glioblastoma* / pathology
  • Glioblastoma* / radiotherapy
  • Histones* / genetics
  • Histones* / metabolism
  • Humans
  • Neoplasm Proteins* / genetics
  • Neoplasm Proteins* / metabolism
  • Neoplastic Stem Cells* / metabolism
  • Neoplastic Stem Cells* / pathology
  • Radiation Tolerance*
  • Spheroids, Cellular / metabolism
  • Spheroids, Cellular / pathology

Substances

  • Biomarkers, Tumor
  • H2AX protein, human
  • Histones
  • Neoplasm Proteins