Dna Damage, Micronucleus Formation, And Cell Death from ¹²⁵I Decays in Dna

References

• Obe G., Johannes C., Schulte-Frohlinde D. DNA double-strand breaks induced by sparsely ionizing radiation and endonucleases as critical lesions in cell death, chromosomal aberrations, mutations and oncogenic transformation. Mutagenesis 1992; 7: 3–12
   PubMed Web of Science ®Google Scholar
• Hofer K. G., Hughes W. L. Radiotoxicity of intranuclear tritium 125-iodine and 131-iodine. Radiat Res 1971; 47: 94–109
   PubMed Web of Science ®Google Scholar
• Feinendegen L. E., Ertl H. H., Bond V. P. Biological toxicity associated with the Auger effect. Biophysical Aspects of Radiation Quality. IAEA, Vienna 1971; 419–30
   Google Scholar
• Hofer K. G., Harris C. R., Smith J. M. Radiotoxicity of intracellular 67Ga 125I and 3H: Nuclear versus cytoplasmic radiation effects in murine L1210 leukemia. Int J Radiat Biol 1975; 28: 225–41
   Web of Science ®Google Scholar
• Kassis A. I., Sastry K. S. R., Adelstein S. J. Kinetics of uptake, retention, and radiotoxicity of 125IUdR in mammalian cells: Implications of localized energy deposition by Auger processes. Radiat Res 1987; 109: 78–89
   PubMed Web of Science ®Google Scholar
• Yasui L. S., Paschoa A. S., Warters R. L., Hofer K. G. Cytotoxicity of 125I decay produced lesions in chromatin. DNA damage by Auger emitters, K. F. Baverstock, D. E. Charlton. Taylor and Francis, London 1988; 181–189
   Google Scholar
• Charlton D. E., Booz J. A Monte Carlo treatment of the decay of 125I. Radiat Res 1981; 87: 10–23
   PubMed Web of Science ®Google Scholar
• Krisch R. E., Sauri C. J. Further studies of DNA damage and lethality from the decay of iodine-125 in bacteriophages. Int J Radiat Biol 1975; 27: 553–60
   Web of Science ®Google Scholar
• Radford I. R., Hodgson G. S., Matthews J. P. Critical DNA target size model of ionizing radiation-induced mammalian cell death. Int J Radiat Biol 1988; 54: 63–79
   PubMed Web of Science ®Google Scholar
• Hofer K. G., Van Loon N., Schneiderman M. H., Charlton D. E. The paradoxical nature of DNA damage and cell death induced by 125I decay. Radiat Res 1992; 130: 121–4
   PubMed Web of Science ®Google Scholar
• Hofer K. G., VanLoon N., Schneiderman M. H., Charlton D. E. High and low-LET cytocidal effects of DNA-associated iodine-125. Biophysical aspects of Auger processes, R. W. Howell, V. R. Narra, K. S. R. Sastry, D. V. Rao. American Institute of Physics. Inc., Woodburry, NY 1992; 227–48
   Google Scholar
• Hofer K. G., Bao S. P. Low-LET and high-LET radiation action of 125I decays in DNA: Effect of cysteamine on micronucleus formation and cell death. Radiat Res 1995; 141: 183–92
   PubMed Web of Science ®Google Scholar
• Nestmann E. R., Brillinger R. L., Gilman J. P. W., Rudd C. J., Swierenga S. H. H. Recommended protocols based on a survey of current practice in genotoxicity testing laboratories: II Mutation in Chinese hamster ovary V79 Chinese hamster lung and L5I78Y mouse lymphoma cells. Mutat Res 1991; 246: 255–84
   PubMedGoogle Scholar
• Schneiderman M. H., Hofer K. G. Schneiderman GS An in vitro 125IUdR-release assay for measuring the kinetics of cell death. Int J Radiat Biol 1991; 59: 397–408
   PubMed Web of Science ®Google Scholar
• Keough W. G., Hofer K. G. An improved method for synthesis and purification of 125l or 131l labeled carrier-free 5-iodo-2'-deoxyuridine. J Lab Comp Radiopharm 1978; 14: 83–90
   Web of Science ®Google Scholar
• Wakata A., Sasaki M. S. Measurement of micronuclei by cytokinesis-block method in cultured Chinese hamster cells: comparison with types and rates of chromosome aberrations. Mutat Res 1987; 190: 51
   PubMed Web of Science ®Google Scholar
• Bradley M. O., Kohn K. W. X-ray induced DNA double strand break production and repair in mammalian cells as measured by neutral filter elution. Nucleic Acids Res 1979; 7: 793–804
   PubMed Web of Science ®Google Scholar
• Okayasu R., Bloecher D., Iliakis G. Variations through the cell cycle in the dose-response of DNA neutral filter elution in X-irradiated synchronous CHO cells. Int J Radiat Biol 1988; 53: 729–47
   Web of Science ®Google Scholar
• Elkind M. M., Sutton H. X-ray damage and recovery in mammalian cells in culture. Nature 1959; 184: 1293–5
   PubMed Web of Science ®Google Scholar
• Iliakis G., Okayasu R., Seaner R. Radiosensitive xrs-5 and parental CHO cells show identical DNA neutral filter elution dose-response: implication for a relationship between cell radiosensitivity and induction of DNA double-strand breaks. Int J Radiat Biol 1988; 54: 55–62
   PubMed Web of Science ®Google Scholar
• Radford I. R. Evidence for a general relationship between the induced level of DNA double-strand breakage and cell killing after X-irradiation of mammalian cells. Int J Radiat Biol 1986; 49: 611–20
   Google Scholar
• Smeets M FMA, Mooren E. H. M., Begg A. C. Radiation-induced DNA damage and repair in radiosensitive and radioresistant human tumor cells measured by field inversion gel electrophoresis. Int J Radiat Biol 1993; 63: 703–13
   PubMed Web of Science ®Google Scholar
• Tobi S. E., Itzhaki R. F. DNA double-strand breaks measured by pulse-field gel electrophoresis in irradiated lymphocytes from normal humans and those with Alzheimer's disease. Int J Radiat Biol 1993; 63: 617–22
   PubMed Web of Science ®Google Scholar
• Warters R. L., Axtell J. Repair of DNA strand break at hyperthermic temperatures in Chinese hamster ovary cells. Int J Radiat Biol 1992; 61: 43–8
   PubMed Web of Science ®Google Scholar
• Alper T. Cellular radiobiology. Cambridge University Press, Cambridge 1979
   Google Scholar
• Elkind M. M., Redpath J. I. Molecular and cellular biology of radiation lethality. Cancer-A comprehensive treatise, F. F. Becker. Martinus Nijhoff., Amsterdam 1983; Vol. 6: 225–30
   Google Scholar
• Dewey W. C., Miller HH, Leeper D. P. Chromosomal aberrations and mortality of X-irradiated mammalian cells: emphasis on repair. Proc Nat Acad Sci USA 1971; 68: 667–71
   PubMed Web of Science ®Google Scholar
• Cornforth M. N., Bedford J. S. A quantitative comparison of potentially lethal damage repair and the rejoining of interphase chromosome breaks in low passage normal human fibroblasts. Radiat Res 1987; 111: 385–405
   PubMed Web of Science ®Google Scholar
• Savage J. R. K. A comment on the quantitative relationship between micronuclei and chromosome aberrations. Mutat Res 1988; 207: 33–6
   PubMed Web of Science ®Google Scholar
• Carrano A. V., Heddle J. A. The fate of chromosome aberrations. J Theor Biol 1973; 38: 289–304
   PubMed Web of Science ®Google Scholar
• Bouffier S., Silver A., Cox R. The role of DNA repeats and associated secondary structures in genomic instability and neoplasia. BioEssays 1993; 15: 409–12
   PubMedGoogle Scholar
• Nelson W. G., Pienta K. J., Barrack E. R., Coffey D. S. The role of the nuclear matrix in the organization and function of DNA. Ann Rev Biophys Chem 1986; 15: 457–75
   PubMedGoogle Scholar