RBE—LET Relationships for Different Types of Lethal Radiation Damage in Mammalian Cells: Comparison with DNA Dsb and an Interpretation of Differences in Radiosensitivity

References

• Barendsen G.W. Influence of radiation quality on the effectiveness of small doses for induction of reproductive death and chromosome aberrations in mammalian cells. International Journal of Radiation Biology 1979; 36: 49–63
   Web of Science ®Google Scholar
• Barendsen G.W. Dose fractionation, dose rate and isoeffect relationships for normal tissue responses. International Journal of Radiation Oncology, Biology and Physics 1982; 8: 1981–1997
   PubMed Web of Science ®Google Scholar
• Barendsen G.W. Mechanisms of cell reproductive death and shapes of radiation dose-survival curves of mammalian cells. International Journal of Radiation Biology 1990; 63: 885–896
   Google Scholar
• Barendsen G.W. Sublethal damage and DNA double-strand breaks have similar RBE-LET relationships: evidence and implications. International Journal of Radiation Biology 1993; 63: 325–330
   PubMed Web of Science ®Google Scholar
• Barendsen G.W. RBE-LET relationships for different types of lethal damage in mammalian cells: biophysical and molecular mechanisms. Radiation Research 1994; 139: 257–270
   PubMed Web of Science ®Google Scholar
• Battermann J.J., Breur K., Hart A.A.M., Van Peperzeel H.A. Observations on pulmonary metastases in patients after single doses and multiple fractions of fast neutrons and Cobalt-60 gamma rays. European Journal of Cancer 1981; 17: 539–545
   PubMed Web of Science ®Google Scholar
• Bedford J. Sublethal damage, potentially lethal damage and chromosomal aberrations in mammalian cells exposed to ionizing radiations. International Journal of Radiation Oncology, Biology and Physics 1991; 21: 1457–1469
   PubMed Web of Science ®Google Scholar
• Bertsche U., Iliakis G. Modifications in repair and expression of potentially lethal damage (α-PLD) as measured by delayed plating or treatment with β-araA in plateau-phase Ehrlich ascites tumor cells after exposure to charged particles of various specific energies. Radiation Research 1987; 111: 26–46
   PubMed Web of Science ®Google Scholar
• Bird R.P., Zaider M., Rossi H.H., Marino N., Rohrig N., Hall E.J. The sequential irradiation of mammalian cells with X-rays and charged particles of high LET. Radiation Research 1983; 93: 444–452
   PubMed Web of Science ®Google Scholar
• Brenner D.J., Ward J.F. Constraints on energy deposition and target size of multiply damaged sites associated with DNA double-strand breaks. International Journal of Radiation Biology 1992; 61: 737–748
   PubMed Web of Science ®Google Scholar
• Broerse J.J., Barendsen G.W. Relative biological effectiveness of fast neutrons for effects on normal tissues. Current Topics in Radiation Research Quarterly 1973; 8: 305–350
   PubMedGoogle Scholar
• Charlton D.E., Nikjoo N., Humm J.L. Calculation of initial yields of single- and double-strand breaks in DNA of cell nuclei from electrons, protons and alpha particles. International Journal of Radiation Biology 1989; 56: 1–19
   PubMed Web of Science ®Google Scholar
• Cox R. A cellular description of the repair defect in ataxia-telangiectasia. Ataxia-Telangiectasia: A Cellular and Molecular Link Between Cancer, Neuropathology and Immune Deficiency, B.A. Bridges, D.G. Harnden. Wiley, London 1982; 141–153, In
   Google Scholar
• Cox R., Thacker J., Goodhead D.T., Munson R.J. Mutation and inactivation of mammalian cells by various ionizing radiations. Nature 1977; 267: 425–427
   PubMed Web of Science ®Google Scholar
• Deacon J., Peckham M.J., Steel G.G. The radioresponsiveness of human tumours and the initial slope of the cell survival curve. Radiotherapy and Oncology 1984; 2: 317–323
   PubMed Web of Science ®Google Scholar
• Fertil B., Malaise E.P. Inherent cellular radiosensitivity as a basic concept for human tumour radiotherapy. International Journal of Radiation Oncology, Biology and Physics 1981; 7: 621–629
   PubMed Web of Science ®Google Scholar
• Fertil B., Deschavanne P.J., Debieu D., Malaise E.P. Correlation between PLD repair and survival curves of human fibroblasts in exponential growth phase: analysis in terms of several parameters. Radiation Research 1988; 116: 74–88
   PubMed Web of Science ®Google Scholar
• Iliakis G. Radiation-induced potentially lethal damage: DNA lesions susceptible to fixation. International Journal of Radiation Biology 1988; 53: 541–584
   Web of Science ®Google Scholar
• Jenner T.J., De Lara C.M., O'Neill P., Stevens D.L. The induction and rejoining of DNA double-strand breaks in V79- mammalian cells by γ- and α-irradiation. International Journal of Radiation Biology 1993; 61: 631–637
   Google Scholar
• Prise K.M., Davies S., Michael B.D. The relationship between radiation-induced DNA double-strand breaks and cell kill in hamster V79 fibroblasts irradiated with 250kVp X-rays, 2·3MeV neutrons or 238Pu α-particles. International Journal of Radiation Biology 1987; 52: 893–902
   Web of Science ®Google Scholar
• Ward J.F. The yield of DNA double-strand breaks produced intra-cellularly by ionizing radiation: a review. International Journal of Radiation Biology 1990; 57: 1141–1150
   PubMed Web of Science ®Google Scholar
• Warenius H.M., Britten R.A., Peacock J.H. The relative cellular radiosensitivity of 30 human in vitro cell lines of different histological type to high-LET 62·5 MeV (p— > Be+) fast neutrons and 4 MeV photons. Radiotherapy and Oncology 1994; 30: 83–89
   PubMed Web of Science ®Google Scholar
• Yang T.C., Craise L.M., Mei M.T., Tobias C.A. Neoplastic cell transformation by heavy charged particles. Radiation Research 1985; 104: S177–S187
   Web of Science ®Google Scholar