Calcium Antagonist, TMB-8, Prevents the Induction of Adaptive Response by Hydrogen Peroxide or X-rays in Human Lymphocytes

References

• Benyajati C., Worcel A. Isolation, characterization and structure of the folded interphase genome of Drosophila melanogaster. Cell 1976; 9: 393–407
   PubMed Web of Science ®Google Scholar
• Boerrigter M.E.T.J. DNA strand break metabolism in human lymphocytes: a reevaluation. Experimental Cell Research 1991; 196: 1–5
   PubMed Web of Science ®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
• Boużyk E., Rosiek O., Wojewodzka M. Small doses of X-rays make human peripheral blood lymphocytes less sensitive to induction of chromatid aberrations by a subsequent large dose of this radiation. Nukleonika 1989; 34: 323–329
   Web of Science ®Google Scholar
• Boużyk E., Rosiek O., Wojewodzka M. Hydrogen peroxide-induced adaptive response in human lymphocytes. Nukleonika 1990; 35: 236–244
   Google Scholar
• Christiansen N.O., Larsen C.S., Juhl H. Ca2+ and phorbol ester activation of protein kinase C at intracellular Ca2+ concentrations and the effect of TMB-8. Biochimica et Biophysica Acta 1986; 882: 57–62
   PubMedGoogle Scholar
• Cook P.R., Brazell I.A. Supercoils in human DNA. Journal of Cell Science 1975; 19: 261–279
   PubMed Web of Science ®Google Scholar
• Cook P.R., Brazell I.A. Conformational constrains in nuclear DNA. Journal of Cell Science 1976; 22: 287–302
   PubMed Web of Science ®Google Scholar
• Cortes F., Dominguez I., Pinero J., Mateos J.C. Adaptive response in human lymphocytes conditioned with hydrogen peroxide before irradiation with X-rays. Mutagenesis 1990; 5: 555–557
   PubMed Web of Science ®Google Scholar
• Fenech M., Morley A.A. Measurement of micronuclei in lymphocytes. Mutation Research 1985; 147: 29–36
   PubMed Web of Science ®Google Scholar
• Grynkiewicz G., Poenie M., Tsien R.Y. A new generation of Ca2+ indicators with greatly improved fluorescence properties. Journal of Biological Chemistry 1985; 260: 3440–3450
   PubMed Web of Science ®Google Scholar
• Hartwig M. Additional folding of nuclear DNA is an early event during stimulation of human lymphocytes. Biomedica et Biochemica Acta 1986; 45: K75–K18
   Google Scholar
• Hartwig M., Körner I.J. Age-related changes of DNA winding and repair in human peripheral lymphocytes. Mechanisms of Ageing and Development 1987; 38: 73–78
   PubMed Web of Science ®Google Scholar
• Heussen C., Nackerdien Z., Smit B.J., Bohm L. Irradiation damage in chromatin isolated from V-79 Chinese hamster lung fibroblasts. Radiation Research 1987; 110: 84–94
   PubMed Web of Science ®Google Scholar
• Ikushima T. Radioadaptive response: involvement of induction of specific gene expression by low doses of ionizing radiation. Low Dose Irradiation and Biological Defence Mechanisms, T. Sugahara, L.A. Sagan, T. Aoyama. Elsevier, Amsterdam 1992; 255–258, In
   Google Scholar
• Kleczkowska H.E., Althaus F.R. Adaptive response of human keratinocytes to low doses of MNNG. Low Dose Irradiation and Biological Defence Mechanisms, T. Sugahara, L.A. Sagan, T. Aoyama. Elsevier, Amsterdam 1992; 275–278, In
   Google Scholar
• Kojima I., Shibata H., Ogata E. Action of TMB-8 (8-(N,N-diethylamino) octyl-3,4,5-trimethoxybenzoate) on cytoplasmic free calcium in adrenal glomerulosa cell. Biochimica et Biophysica Acta 1986; 888: 25–29
   PubMedGoogle Scholar
• Laval F. Pretreatment with oxygen species increases the resistance of mammalian cells to hydrogen peroxide and γ-rays. Mutation Research 1988; 201: 73–79
   PubMedGoogle Scholar
• Meyers M., Schea R.A., Petrowski A.E., Seabury H., McLaughlin P.W., Lee I., Lee S.W., Boothman D.A. Role of X-ray-inducible genes and proteins in adaptive survival responses. Low Dose Irradiation and Biological Defence Mechanisms, T. Sugahara, L.A. Sagan, T. Aoyama. Elsevier, Amsterdam 1992; 263–266, In
   Google Scholar
• Mix L.L., Dinerstein R.J., Villereal M.L. Mitogens and melittin stimulate an increase in intracellular free calcium concentration in human fibroblasts. Biochimica and Biophysic Research Communications 1984; 119: 69–75
   PubMed Web of Science ®Google Scholar
• Mullenders L.H.F., van Zeeland A.A., Natarajan A.T. Comparison of DNA loop size and supercoiled domain size in human cells. Mutation Research 1983; 112: 242–252
   Google Scholar
• Nackerdien Z., Michie J., Bohm L. Chromatin decondensed by acetylation shows an elevated radiation response. Radiation Research 1989; 117: 234–244
   PubMed Web of Science ®Google Scholar
• Olivieri G., Bosi A. Possible causes of variability of the adaptive response in human lymphocytes. Chromosomal Aberrations, A.T. Natarajan, G. Obe. Springer, Berlin 1989; 140–151, In
   Google Scholar
• Palmer F.B., Byers D.M., Spence M.W., Cook H.W. Calcium-independent effects of TMB-8. Biochemical Journal 1992; 286: 505–512
   PubMed Web of Science ®Google Scholar
• Roti-Roti J.L., Painter R.B. Effects of hyperthermia on the sedimentation of nucleoids from HeLa cells in sucrose gradients. Radiation Research 1982; 89: 166–175
   PubMed Web of Science ®Google Scholar
• Schwartz K., Korner I.J., Gunther K. Determination of the molecular weight of supercoiled DNA subunits by sedimentation of nucleoids from X-irradiated normal and malignant human lymphocytes. Studia Biophysica 1984; 100: 149–159
   Google Scholar
• Simpson A.W.M., Hallam T.J., Rink T.J. TMB-8 inhibits secretion evoked by phorbol ester at basal cytoplasmic free calcium in quin-2 loaded platelets much more effectively than in inhibits thrombin-induced calcium morbilization. FEBS Letters 1984; 176: 139–143
   PubMed Web of Science ®Google Scholar
• Umezawa K., Imoto M., Itoh O., Takeuchi T., Hori M. Inhibitors of oncogene functions from actinomycetes. Horizons on Antibiotic Research, B.D. Davis, T. Ichikawa, K. Maeda, L.A. Mitcher. Japan Antibiotics Research Assoc., Tokyo 1988; 74–87, In
   Google Scholar
• Van Rensburg E.J., Louw W.K.A., Izatt H., van der Watt I.J. DNA supercoiled domains and radiosensitivity of subpopulations of human peripheral blood lymphocytes. International Journal of Radiation Biology 1985; 47: 673–679
   Web of Science ®Google Scholar
• van Rensburg E.J., Louw W.K.A., van der Merwe K.J. Changes in DNA supercoiling during repair of gamma-radiation-induced damage. International Journal of Radiation Biology 1987; 52: 693–703
   Web of Science ®Google Scholar
• Walicka M., Godlewska E. Radiation sensitivities are not related to the sizes of DNA supercoiled domains in L5178Y-R and L5178Y-S cells. International Journal of Radiation Biology 1989; 55: 953–961
   PubMed Web of Science ®Google Scholar
• Warters R.L., Lyons B.W. Variation in radiation-induced formation of double-strand breaks as a function of chromatin structure. Radiation Research 1992; 130: 309–318
   PubMed Web of Science ®Google Scholar
• Weichselbaum R.R., Hallahan D.E., Sukhatme V., Dritschilo A., Sherman M.L., Kufe D.W. Biological consequences of gene regulation after ionizing radiation exposure. Journal of the National Cancer Institute 1991; 83: 480–484
   PubMedGoogle Scholar
• Weiss A., Imboden J., Shobak D., Stobo J. Role of T3 surface molecules in human T-cell activation: T3-dependent activation results in an increase in cytoplasmic free calcium. Proceedings of the National Academy of Sciences, USA 1984; 81: 4169–4173
   PubMed Web of Science ®Google Scholar
• Wolff S. Low-dose exposures and the induction of adaptation. Low Dose Irradiation and Biological Defence Mechanisms, T. Sugahara, L.A. Sagan, T. Aoyama. Elsevier, Amsterdam 1992; 21–28, In
   Google Scholar
• Wolff S., Olivieri G., Afzal V. Adaptation of human lymphocytes to radiation or chemical mutagens: differences in cytogenetic repair. Chromosomal Aberrations, A.T. Natarajan, G. Obe. Springer, Berlin 1990; 140–151, In
   Google Scholar
• Wolff S., Wiencke J.K., Youngblom V., Cortes F. The adaptive response of human lymphocytes to very low doses of ionizing radiation: a case of induced chromosomal repair with the induction of specific proteins. Low Dose Radiation: Biological Bases of Risk Assessment. Taylor & Francis, London 1989; 446–454, In
   Google Scholar
• Woloschak G.E., Chang-Liu C.M. Effects of low-dose radiation on gene expression in Syrian hamster embryo cells: comparison of JANUS neutrons and gamma-rays. Low Dose Irradiation and Biological Defence Mechanisms, T. Sugahara, L.A. Sagan, T. Aoyama. Elsevier, Amsterdam 1992; 239–246, In
   Google Scholar
• Yasui L.S., Higashikubo R., Warters R.L. The effect of chromatin decondensation on DNA damage and repair. Radiation Research 1987; 112: 318–330
   PubMed Web of Science ®Google Scholar
• Zar J.H. Biostatistical Analysis. Prentice Hall, New Jersey 1984; 101–103
   Google Scholar