Skip to main content
Log in

Reduction of nitroxides and radioprotective ability in glioblastoma cells

  • Original Article
  • Published:
Brain Tumor Pathology Aims and scope Submit manuscript

Abstract

Electron spin resonance (ESR) analyses were performed to clarify whether glioblastoma cells scavenge hydroxyl radicals (·OH) generated by x-ray irradiation. The rate of bioreduction of nitroxides by three human glioblastoma cells was also evaluated by the same technique and compared with their x-ray sensitivity. Aerated culture media containing 200 mM of 5,5-dimethyl-1-pyrroline-N-oxide (DMPO) with or without U87MG cells were irradiated with x-rays at a dose of 20 Gy. ESR was measured immediately after each irradiation. Continuous changes of the ESR spectra of 4-hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (Tempol) were analyzed in cell suspensions of TK1, U87MG, and A172 at a concentration of 1.0×107 cells/ml containing 5 μM Tempol. As a result, the signal of DMPO-OH in the U87MG cell suspension decayed faster than that in the control culture media without cells, and the rate of bioreduction of Tempol in each glioblastoma cell suspension was correlated with the x-ray sensitivity defined from the colony-forming assay in those cell lines. It was indicated that the resistance of glioblastoma cells to ionizing radiation could be closely related to their ability to scavenge radical species generated by ionizing radiation.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Hall EJ (1994) Radiobiology for the radiologist. JB Lippincott, Philadelphia, pp 3–15

    Google Scholar 

  2. Roots R, Okada S (1975) Estimation of lifetimes and diffusion distances of radicals involved in x-ray-induced strand breaks or killing of mammalian cells. Radiat Res 64:306–320

    PubMed  CAS  Google Scholar 

  3. Steel GG (2002) Basic clinical radiobiology. Introduction: the significance of radiobiology for radiotherapy. Arnold, London, pp 1–7

    Google Scholar 

  4. Boag JW (1975) The time-scale in radiation biology. 12th Failla Memorial Lecture. In: Nygaard OF, Adler HI, Sinclar WK (eds) Radiation research. Academic Press, San Diego

    Google Scholar 

  5. Chapman JD, Doern SD, Reuvers AP, et al. (1979) Radioprotection by DMSO of mammalian cells exposed to x-rays and to heavy charged-particle beams. Radiat Environment Biophys 16:29–41

    Article  CAS  Google Scholar 

  6. Tsuboi K, Yoshii Y, Nose T (1996) Establishment of a human glioblastoma cell line TK-1. Human Cell 9: 125–127

    PubMed  CAS  Google Scholar 

  7. Westermark B (1973) The deficient density-dependent growth control of human malignant glioma cells and virus-transformed glia-like cells in culture. Int J Cancer 12: 438–445

    PubMed  CAS  Google Scholar 

  8. Bigner SH, Mark J, Bigner DD (1983) Chromosomal composition of four permanent cultured cell lines derived from human gliomas. Cancer Genet Cytogenet 10:335–349

    Article  PubMed  CAS  Google Scholar 

  9. Kubota N, Okada S, Inada T (2000) Wortmannin sensitizes human glioblastoma cell lines carrying mutant and wild type TP53 gene to radiation. Cancer Lett 161:141–147

    Article  PubMed  CAS  Google Scholar 

  10. Takahashi A, Ohnishi K, Wang X, et al. (2000) The difference of p53 on the radiation enhancement of thermosensitivity at different LET. Int J Radiat Oncol Biol Phys 47:489–494

    Article  PubMed  CAS  Google Scholar 

  11. Tribius S, Pidel A, Casper D (2001) ATM protein expression correlates with radioresistance in primary glioblastoma cells in culture. Int J Radiat Oncol Biol Phys 50:511–523

    Article  PubMed  CAS  Google Scholar 

  12. Halliwell B, Gutteridge JMC (1999) Free radicals in biology and medicine. Oxford University Press, New York, pp 351–429

    Google Scholar 

  13. Kocherginsky N, Swartz HM (1995) Nitroxide spin labels: reactions in biology and chemistry. CRC Press, Boca Raton, Florida, 113–147

    Google Scholar 

  14. Swartz HM, Sentjurc M, Morse PD (1986) Cellular metabolism of water-soluble nitroxides: effect on rate of reduction of cell/nitroxide ratio, oxygen concentrations and permeability of nitroxides. Biochem Biophys Acta 888:82–90

    Article  PubMed  CAS  Google Scholar 

  15. Iannone A, Tomashi A (1991) Nitroxide radicals, their use as metabolic probes in biological model systems: an overview. Acta Pharm Jugosl 41:277–297

    CAS  Google Scholar 

  16. Halpern HJ, Jaffe DR, Nguyen TD, et al. (1991) Measurement of bioreduction rates of cells with distinct responses to ionizing radiation and cisplatin. Biochem Biophys Acta 1093: 121–124

    Article  PubMed  CAS  Google Scholar 

  17. Mitchell P (1961) Coupling of phosphorylation to electron and hydrogen transfer by a chemi-osmotic type of mechanism. Nature 191:144–148

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Koji Tsuboi.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Moritake, T., Tsuboi, K., Anzai, K. et al. Reduction of nitroxides and radioprotective ability in glioblastoma cells. Brain Tumor Pathol 20, 1–5 (2003). https://doi.org/10.1007/BF02478940

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02478940

Key words

Navigation