Hypersensitive Response of Normal Human Lung Epithelial Cells at Low Radiation Doses

References

• Bates D.M., Watts D.G. Nonlinear Regression Analysis and its Applications. Wiley, New York 1988
   Google Scholar
• Bedford J.S., Griggs H.G. The estimation of survival at low doses and the limits of resolution of the single-cell-plating technique. Cell Survival After Low Doses of Radiation: Theoretical and Clinical Implications, T. Alper. Wiley, London 1975; 34–39, In
   Google Scholar
• Boag J.W. The statistical treatment of cell survival data. Cell Survival after Low Doses of Radiation: Theoretical and Clinical Implications, T. Alper. Wiley, London 1975; 40–53, In
   Google Scholar
• Boothman D.A., Bouvard I., Hughes E.N. Identification and characterization of X-ray-induced proteins in human cells. Cancer Research 1989; 49: 2871–2878
   PubMed Web of Science ®Google Scholar
• Boothman D.A., Meyers M., Seabury W., McLaughlin P.W. (1993) Role of X-ray-inducible genes and proteins in adaptive survival responses. Abstracts of Papers for the Forty First Meeting of the Radiation Research Society and the Thirteenth Annual Meeting of the North American Hyperthermia Society, Dallas, Texas, March, 20–25, 51–51, In
   Google Scholar
• Bryant P.E. Changes in sensitivity of cells during exposure to radiation at low dose-rate. International Journal of Radiation Biology 1972; 22: 67–73
   Web of Science ®Google Scholar
• Calkins J. An unusual form of response in X-irradiated protozoa and a hypothesis as to its origin. International Journal of Radiation Biology 1967; 12: 297–301
   Web of Science ®Google Scholar
• Calkins J., Todd W. Evidence for a triggered or activated radiation repair system in Saccharomyces cerivisiae. International Journal of Radiation Biology 1968; 4: 487–491
   Google Scholar
• Deschavanne P.J., Debieu D., Fertil B., Malaise E.P. Re-evaluation of in vitro radiosensitivity of human fibroblasts of different genetic origins. International Journal of Radiation Biology 1986; 50: 279–293
   Web of Science ®Google Scholar
• Gupta S.S., Bhattacharjee S.B. Induction of repair functions by hydrogen peroxide in Chinese hamster cells. International Journal of Radiation Biology 1988; 53: 935–942
   Web of Science ®Google Scholar
• Hendry J.H. Radioresistance in fern spores by prior irradiation. Radiation Research 1986; 106: 396–400
   Google Scholar
• Howard A., Cowie F.G. Induced resistance in a Desmid Closterium moniliferum. Radiation Research 1976; 65: 540–549
   PubMed Web of Science ®Google Scholar
• Hughes S.S., Boothman D.A. Effect of caffeine in the expression of a major X-ray-induced protein in human tumour cells. Radiation Research 1991; 125: 313–317
   PubMed Web of Science ®Google Scholar
• Ikushima T. Chromosomal responses to ionizing radiation reminiscent of an adaptive response in cultured Chinese hamster cells. Mutation Research 1987; 180: 215–221
   PubMed Web of Science ®Google Scholar
• JMP®. User's Guide: Version 2 (1989) Software for Statistical Visualization on the Apple Macintosh®. SAS Institute Inc., Cary, NC
   Google Scholar
• Joiner M.C., Denekamp J., Maughan R.L. The use of ‘top-up’ experiments to investigate the effects of very small doses per fraction in mouse skin. International Journal of Radiation Biology 1986; 49: 565–580
   Web of Science ®Google Scholar
• Joiner M.C., Johns H. Renal damage in the mouse: the response to very small doses per fraction. Radiation Research 1988; 114: 385–398
   PubMed Web of Science ®Google Scholar
• Kastan M.B., Zhan Q., Deiry W.S., Carrier F., Jacks T., Walsh W.V., Plunkett B.S., Vogelstein B., Fornace A.J. A mammalian cell cycle check-point pathway utilizing p53 and GADD45 is defective in ataxia-telangiectasia. Cell 1992; 71: 587–597
   PubMed Web of Science ®Google Scholar
• Koval T.M. Multiphasic survival response of a radio-resistant lepidopteran insect cell line. Radiation Research 1984; 98: 642–648
   PubMed Web of Science ®Google Scholar
• Koval T.M. Inducible repair of ionizing radiation damage in higher cukaryotic cells. Mutation Research 1986; 173: 291–293
   PubMed Web of Science ®Google Scholar
• Koval T.M. Enhanced recovery from ionizing radiation damage in lepidopteran insect cell line. Radiation Research 1988; 115: 413–420
   PubMed Web of Science ®Google Scholar
• Kuerbitz S.J., Plunkett B.S., Walsh W.V., Kastan M.B. Wild-type p53 is a cell cycle checkpoint determinant following irradiation. Proceedings of the National Academy of Sciences, USA 1992; 89: 7491–7495
   PubMed Web of Science ®Google Scholar
• Lambin P., Marples B., Fertil B., Malaise E.P., Joiner M.C. Hypersensitivity of a human tumour cell line to very low radiation doses. International Journal of Radiation Biology 1993; 63: 639–650
   PubMed Web of Science ®Google Scholar
• Leenhouts H.P., Susma M.J., Litwiniszyn M., Broerties C., Chadwick H.K. Radiation stimulated repair in Saintpaulia cells in vivo. Radiation Biology and Chemistry, H.E. Edwards, S. Navaratnam, B.J. Parsons, G.O. Phillips. Elsevier, Amsterdam 1979; 227–236, In
   Google Scholar
• Marples B., Joiner M.C. The response of V79 cells to low radiation doses: evidence of enhanced sensitivity of the whole cell population. Radiation Research 1993; 133: 41–51
   PubMed Web of Science ®Google Scholar
• Muschel R.J., Zhang H.B., Iliakis G., McKenna W.G. Effects of ionizing radiation on cyclin expression in HeLa cells. Radiation Research 1992; 132: 153–157
   PubMed Web of Science ®Google Scholar
• Muschel R.J., Zhang H.B., McKenna W.G. Differential effect of ionizing radiation on the expression of cyclin A and cyclin B in HeLa cells. Cancer Research 1993; 53: 1128–1135
   PubMed Web of Science ®Google Scholar
• Olivieri G., Bodycote J., Wolff S. Adaptive response of human lymphocytes to low concentrations of radioactive thymidine. Science 1984; 223: 594–597
   PubMed Web of Science ®Google Scholar
• Palcic B., Jaggi B. The use of solid-state image sensor technology to detect and characterize live mammalian cells growing in tissue culture. International Journal of Radiation Biology 1986; 50: 345–352
   Web of Science ®Google Scholar
• Palcic B., Skarsgard L.D. Reduced oxygen enhancement ratio at low doses of ionizing radiation. Radiation Research 1984; 100: 328–339
   PubMed Web of Science ®Google Scholar
• Puck T.T., Marcus P.I. Action of X-rays on mammalian cells. Journal of Experimental Medicine 1956; 103: 653–666
   PubMed Web of Science ®Google Scholar
• Ratkowski D.A. Handbook of Nonlinear Regression Models. Marcel Dekker, New York 1990
   Google Scholar
• Sankaranarayanan K., Duyn A.V., Loos M.J., Natarajan A.T. Adaptive response of human lymphocytes to low-level radiation from radioisotopes or X-rays. Mutation Research 1989; 211: 7–12
   PubMed Web of Science ®Google Scholar
• Santier S., Gilet R., Malaise E.P. Induced radiation resistance during low-dose rate γ-irradiation in plateau-phase Chlorella cells. Radiation Research 1985; 104: 224–233
   Google Scholar
• Shadley J.D., Afzal V., Wolff S. Characterization of the adaptive response to ionizing radiation induced by low doses of X-rays to human lymphocytes. Radiation Research 1987; 111: 511–517
   PubMed Web of Science ®Google Scholar
• Shadley J.D., Dai G.Q. Cytogenetic and survival adaptive responses in G1 phase human lymphocytes. Mutation Research 1992; 265: 273–281
   PubMed Web of Science ®Google Scholar
• Shadley J.D., Dai G. Evidence that the adaptive response of human lymphocytes to ionizing radiation acts on lethal damage in nonaberrant cells. Mutation Research 1993; 301: 171–176
   PubMed Web of Science ®Google Scholar
• Shadley J.D., Wolff S. Very low doses of X-rays can cause human lymphocytes to become less susceptible to ionizing radiation. Mutagenesis 1987; 2: 95–96
   PubMed Web of Science ®Google Scholar
• Skarsgard L.D., Harrison I., Durand R.E. The radiation response of asynchronous cells at low dose: evidence of substructure. Radiation Research 1991; 127: 248–256
   PubMed Web of Science ®Google Scholar
• Watts M.E., Hodgkiss R.J., Jones N.R., Fowler J.F. Radiosensitization of Chinese hamster cells by oxygen and misonidazole. International Journal of Radiation Biology 1986; 50: 1009–1021
   Web of Science ®Google Scholar
• Wiencke J.K., Afzal V., Olivieri G., Wolff S. Evidence that the [3H]thymidine-induced adaptive response of human lymphocytes to subsequent doses of X-rays involves the induction of a chromosomal repair mechanism. Mutagenesis 1986; 1: 375–380
   PubMed Web of Science ®Google Scholar
• Wolff S. Failla Memorial Lecture. Is radiation all bad? The search for adaptation. Radiation Research 1992; 131: 117–123
   PubMed Web of Science ®Google Scholar
• Wolff S., Afzal V., Wiencke J.K., Olivieri G., Michaeli A. Human lymphocytes exposed to low doses of ionizing radiations become refractory to high doses of radiation as well as to chemical mutagens that induced double-strand breaks in DNA. International Journal of Radiation Biology 1988; 53: 39–55
   Web of Science ®Google Scholar
• Woloschak G.E., Chang-Liu C.M., Shearin-Jones P. Regulation of Protein Kinase C by ionizing radiation. Cancer Research 1990; 50: 3963–3967
   PubMed Web of Science ®Google Scholar