¹²⁵IdUrd-induced Chromosome Fragments, Assayed by Premature Chromosome Condensation, and DNA Double-strand Breaks Have Similar Repair Kinetics in G₁-phase CHO-cells

References

• Ahnstrom G., Ehrenberg L.E., Hussain S., Natarajan A.T. On the killing and mutagenic action in E. coli associated with the Auger effect during 125I decay. Mutation Research 1970; 10: 247–250
   PubMedGoogle Scholar
• Blocher D., Pohlit W. DNA double strand breaks in Ehrlich ascites tumour cells at low doses of X-rays. II. Can cell death be attributed to double strand breaks?. International Journal of Radiation Biology 1982; 42: 329–338
   Web of Science ®Google Scholar
• Borrelli M.J., Mackey M.A., Dewey W.C. A method for freezing synchronous mitotic and G1-cells. Experimental Cell Research 1987; 170: 363–368
   PubMed Web of Science ®Google Scholar
• Bradley E.W., Chan P.C., Adelstein S.J. The radiotoxicity of iodine-125 in mammalian cells. I. Effects on the survival curve of radioiodine incorporated into DNA. Radiation Research 1975; 64: 555–563
   PubMed Web of Science ®Google Scholar
• Bradley M.V., Kohn K.W. X-ray induced DNA double strand break production and repair in mammalian cells as measured by neutral filter elution. Nucleic Acid Research 1979; 7: 793–804
   PubMed Web of Science ®Google Scholar
• Bryant P.E. Enzymatic restriction of mammalian cell DNA using PyuII and Bam H1: Evidence for the double-strand break origin of chromosomal aberrations. International Journal of Radiation Biology 1984; 46: 57–65
   Web of Science ®Google Scholar
• Bryant P.E. Enzymatic restriction of mammalian cell DNA: Evidence for double-strand breaks as potentially lethal lesions. International Journal of Radiation Biology 1985; 48: 55–60
   Web of Science ®Google Scholar
• Bryant P.E., Blocher D. Measurement of the kinetics of DNA double strand break repair in Ehrlich ascites tumour cells using the unwinding method. International Journal of Radiation Biology 1980; 38: 335–347
   Web of Science ®Google Scholar
• Burki H.J., Koch C., Wolff S. Molecular suicide studies of 125I and 3H disintegration in the DNA of Chinese hamster cells. Current Topics in Radiation Research 1977; Q12: 408–425
   Google Scholar
• Burki H.J., Roots R., Feinendegen L.E., Bond V.P. Inactivation of mammalian cells after disintegrations of 3H or 125I in cell DNA at -146°C. International Journal of Radiation Biology 1973; 24: 363–375
   Web of Science ®Google Scholar
• Chan P.C., Lisco E., Lisco H., Adelstein S.J. The radiotoxicity of iodine-125 in mammalian cells. II. A comparative study on cell survival and cytogenetic responses to 125IdUrd and 131IdUrd and 3H TdR. Radiation Research 1976; 67: 332–343
   PubMed Web of Science ®Google Scholar
• Charlton D.E. The range of high LET effects from 125I-decays. Radiation Research 1986; 107: 163–171
   PubMed Web of Science ®Google Scholar
• Charlton D.E., Booz J. A Monte Carlo treatment of the decay of 125I. Radiation Research 1981; 87: 10–23
   PubMed Web of Science ®Google Scholar
• Charlton D.E., Booz J., Fidorra J., Smith T., Feinendegen L.C. Microdosimetry of radioactive nuclei incorporated into the DNA of mammalian cells. Proceedings, Sixth Symposium of Microdosimetry, Brussels, J. Booz, H.G. Ebert. Commission of the European Communities, EUR 6064 d-e-f, London 1978; 91–110
   Google Scholar
• Cleaver J.E., Thomas G.H., Burki H.J. Biological damage from intranuclear tritium: DNA strand breaks and their repair. Science 1972; 177: 996–998
   PubMed Web of Science ®Google Scholar
• Cornforth M.N., Bedford J.S. X-ray induced breakage and rejoining of human interphase chromosomes. Science 1983; 222: 1141–1143
   PubMed Web of Science ®Google Scholar
• Dewey W.C. Confirmation of lesions having the potential for forming chromosomal aberrations. International Journal of Radiation Biology 1972; 22: 95–97
   Google Scholar
• Dewey W.C., Furman S.C., Miller H.H. Comparison of lethality and chromosome damage induced by x-rays in synchronized Chinese hamster cells in vitro. Radiation Research 1970; 43: 561–581
   PubMed Web of Science ®Google Scholar
• Dewey W.C., Miller H.H., Leeper D.B. Chromosomal aberrations and mortality of x-irradiated mammalian cells: emphasis on repair. Proceedings of the National Academy of Science, U.S.A. 1971; 68: 667–671
   PubMed Web of Science ®Google Scholar
• Hahn G.M., Little J.B. Plateau-phase cultures of mammalian cells: An in vitro model for human cancer. Current Topics of Radiation Research 1972; Q8: 39–83
   Google Scholar
• Hittelman W.N., Pollard M. A comparison of the DNA and chromosome repair kinetics after gamma-irradiation. Radiation Research 1982; 92: 497–509
   PubMed Web of Science ®Google Scholar
• Hittelman W.N., Rao P.N. Premature chromosome condensation: I. Visualization of gamma-ray-induced chromosome damage in interphase cells. Mutation Research 1974; 23: 251–258
   PubMed Web of Science ®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 leukaemia. International Journal of Radiation Biology 1975; 28: 225–241
   Web of Science ®Google Scholar
• Hofer K.G., Keough G., Smith J.M. Biological toxicity of Auger emitters: Molecular fragmentation versus electron irradiation. Current Topics in Radiation Research 1977; Q12: 335–354
   Google Scholar
• Iliakis G., Pohlit W. Quantitative aspects of repair of potentially lethal damage in mammalian cells. International Journal of Radiation Biology 1979; 36: 649–658
   Web of Science ®Google Scholar
• Johnson R.T., Rao P.N. Mammalian cell fusion: Induction of premature chromosome condensation in interphase nuclei. Nature (London) 1970; 226: 717–722
   PubMed Web of Science ®Google Scholar
• Kawamoto J.C., Barrett J.N. Cryopreservation of primary neurons for tissue culture. Brain Research 1986; 384: 84–93
   PubMedGoogle Scholar
• Kemp L.M., Sedgwick S.G., Jeggo P.A. X-ray sensitive mutants of Chinese hamster ovary cells defective in double-strand break rejoining. Mutation Research 1984; 132: 189–196
   PubMed Web of Science ®Google Scholar
• Kirsch R.E. Lethal effects of iodine-125 decay by electron capture in Escherichia coli and in bacteriophage. International Journal of Radiation Biology 1972; 21: 167–189
   Google Scholar
• Kirsch R.E., Sauri C.J. Further studies of DNA damage and lethality from the decay of iodine-125 in bacteriophages. International Journal of Radiation Biology 1975; 27: 553–560
   Google Scholar
• Kirsch R.E., Krasin E., Sauri C.J. DNA breakage, repair and lethality accompanying 125I decay in microorganisms. Current Topics in Radiation Research 1977; Q12: 355–368
   Google Scholar
• Koch C.J., Burki H.J. The oxygen-enhancement ratio for reproductive death induced by 3H or 125I damage in mammalian cells. International Journal of Radiation Biology 1975; 28: 417–425
   Web of Science ®Google Scholar
• LeMotte P.K., Little J.B. DNA damage induced in human diploid cells by decay of incorporated radionuclides. Cancer Research 1984; 44: 1337–1342
   PubMed Web of Science ®Google Scholar
• LeMotte P.K., Little J.B. A comparison of the lethal effects of intracellular radionuclides in human and rodent cells. Radiation Research 1985; 95: 359–369
   Google Scholar
• Martin R.F., Haseltine W.A. Range of radiochemical damage to DNA with decay of iodine-125. Science 1981; 213: 896–898
   PubMed Web of Science ®Google Scholar
• Miyazaki N., Fujiwara Y. Mutagenic and lethal effects of (5-125I) iodo-2′-deoxyuridine incorporated into DNA of mammalian cells, and their RBE's. Radiation Research 1981; 88: 456–465
   PubMed Web of Science ®Google Scholar
• Natarajan A.T., Obe G. Molecular mechanisms involved in the production of chromosomal aberrations. III. Restriction endonucleases. Chromosoma (Berlin) 1984; 90: 120–127
   PubMed Web of Science ®Google Scholar
• Natarajan A.T., Obe G., van Zeeland A.A., Palitti F., Meijers M., Verdegaal-Immerzel E.A.M. Molecular mechanisms involved in the production of chromosomal aberrations: II. Utilization of neurospora endonuclease for the study of aberration production by X-rays in G1 and G2 stages of the cell cycle. Mutation Research 1980; 69: 293–305
   PubMed Web of Science ®Google Scholar
• Painter R.B., Young B.R., Burki H.J. Non-repairable strand breaks induced by 125I incorporated into mammalian DNA. Proceedings of the National Academy of Science, U.S.A. 1974; 71: 4836–4838
   PubMed Web of Science ®Google Scholar
• Pantelias G.E., Maillie H.D. A simple method for premature chromsome condensation induction in primary human and rodent cells using polyethylene glycol. Somatic Cell Genetics 1983; 9: 533–547
   PubMedGoogle Scholar
• Phillips R.A., Tolmach L.J. Repair of potentially lethal damage in x-irradiated HeLa cells. Radiation Research 1966; 29: 413–432
   PubMed Web of Science ®Google Scholar
• Puck T.T. Action of radiation on mammalian cells. III. Relationship between reproductive death and induction of chromosome anomalies by x-irradiation of euploid human cells in-vitro. Proceedings of the National Academy of Science, U.S.A. 1958; 44: 772–780
   PubMedGoogle Scholar
• Radford I.R., Hodgson G.S. 125I-induced DNA double strand breaks: Use in calibration of the neutral filter elution technique and comparison with x-ray induced breaks. International Journal of Radiation Biology 1985; 48: 555–566
   Web of Science ®Google Scholar
• Raju M.R., Frank J.P., Bain E., Trujillo T.T., Tobey R.A. Repair of potentially lethal damage in Chinese hamster cells after X and alpha irradiation. Radiation Research 1977; 71: 614–621
   PubMed Web of Science ®Google Scholar
• Ritter M.A. The radiotoxicity of iodine-125 in ataxia telangiectasia fibroblasts. Biochimica and Biophysica Acta 1981; 652: 151–159
   PubMedGoogle Scholar
• Schmidt A., Holtz G. The occurrence of double-strand breaks in coliphage T1-DNA by iodine-125 decay. International Journal of Radiation Biology 1973; 24: 307–313
   Web of Science ®Google Scholar
• Scott D. Chromosomal responses of radiosensitive cells. Radiation-induced Chromosome Damage in Man, T. Ishihara, M.S. Sasaki. Alan R. Liss, New York 1983; 141–165
   Google Scholar
• Sundell-Bergman S., Johanson K.J. Repairable and unrepairable DNA strand breaks induced by decay of 3H and 125I incorporated into DNA of mammalian cells. Radiation and Environmental Biophysics 1980; 18: 239–248
   PubMed Web of Science ®Google Scholar
• Waldren C.A., Johnson R.T. Analysis of interphase chromosome damage by means of premature chromosome condensation after gamma- and ultraviolet-irradiation. Proceedings of the National Academy of Sciences, U.S.A. 1974; 71: 1137–1141
   PubMed Web of Science ®Google Scholar
• Ward J.F., Blakely W.F., Joner E.I. Mammalian cells are not killed by DNA single-strand breaks caused by hydroxyl radicals from hydrogen peroxide. Radiation Research 1985; 103: 383–392
   PubMed Web of Science ®Google Scholar
• Weibezahn K.F., Coquerelle T. Radiation induced DNA double strand breaks are rejoined by ligation and recombination processes. Nucleic Acids Research 1981; 9: 3139–3150
   PubMed Web of Science ®Google Scholar
• Woods W.G. Quantitation of the repair of gamma-radiation-induced double-strand DNA breaks in tumor fibroblasts. Biochimica et Biophisica Acta 1981; 655: 342–348
   PubMed Web of Science ®Google Scholar