Cellularly Generated Active Oxygen Species and Hela Cell Proliferation

References

• Oberley L. W., Buettner G. R. Role of superoxide dismutase in cancer: a review. Cancer Research 1979; 39: 1141–1149
   PubMed Web of Science ®Google Scholar
• Sun Y. Free radicals, antioxidant enzymes and carcinogenesis. Free Radical Biology and Medicine 1990; 8: 583–599
   PubMed Web of Science ®Google Scholar
• Church S. L., Grant J. W., Ridnour L. A., Oberley L. W., Swanson P. E., Meltzer P. S., Trent J. M. Increased manganese superoxide dismutase expression suppresses the malignant phenotype of human melanoma cells. Proceedings of the National Academy of Sciences, USA 1993; 90: 3113–3117
   PubMed Web of Science ®Google Scholar
• Burdon R. H., Gill V., Rice‐Evans C. Cell Proliferation and oxidative stress. Free Radical Research Communications 1989; 7: 149–159
   PubMed Web of Science ®Google Scholar
• Burdon R. H., Gill V., Rice‐Evans C. Oxidative stress and tumour cell proliferation. Free Radical Research Communications 1990; 11: 65–76
   PubMed Web of Science ®Google Scholar
• Crawford D., Zbinden I., Amstad P., Cerutti P. Oxidant stress induces the protooncogenes c‐fos and c‐myc in mouse epidermal cells. Oncogene 1988; 3: 27–32
   Web of Science ®Google Scholar
• Shibanuma M., Kuroki T., Nose K. Stimulation by hydrogen peroxide of DNA synthesis competence family gene expression and phosphorylation of a specific protein in quiescent Balb/3T3 cells. Oncogene 1990; 5: 1025–1032
   PubMed Web of Science ®Google Scholar
• Murrell G. A.C., Francis M. J.O., Bromley L. Modulation of fibroblast proliferation by oxygen free radicals. Biochemical Journal 1990; 265: 659–665
   PubMed Web of Science ®Google Scholar
• Meier B., Radeke H. H., Selle S., Younes M., Seis H., Resch K., Habermehl G. G. Human fibroblasts release reactive oxygen species in response to interleukin‐1 or tumour necrosis factor‐α. Biochemical Journal 1989; 263: 539–545
   PubMed Web of Science ®Google Scholar
• Matsuyama T., Ziff M. Increased superoxide anion release from human endothelial cells in response to cytokines. Journal of Immunology 1986; 137: 3295–3304
   PubMedGoogle Scholar
• Burdon R. H. Cell proliferation and oxidative stress: basis for anticancer drugs. Proceedings of the Royal Society of Edinburgh 1992; 99B: 169–176
   Google Scholar
• Takasu N., Komatsu M., Aizawa T., Yamada T. Hydrogen peroxide generation in whole rat pancreatic islets: synergistic regulation by cytoplasmic free calcium and protein kinase C. Biochemical and Biophysical Research Communications 1988; 155: 569–575
   PubMed Web of Science ®Google Scholar
• Szatrowski T. P., Nathan C. F. Production of large amounts of hydrogen peroxide by human tumour cells. Cancer Research 1991; 51: 794–798
   PubMed Web of Science ®Google Scholar
• Burdon R. H., Gill V., Rice‐Evans C. Reduction of a tetrazolium salt and superoxide generation in human tumour cells (HeLa). Free Radical Research Communications 1993, in press
   Google Scholar
• Dionisi O., Galeotti T., Terranova T., Azzi A. Superoxide radicals and hydrogen peroxide formation in mitochondria from normal and neoplastic tissue. Biochimica et Biophysica Acta 1975; 403: 292–300
   PubMed Web of Science ®Google Scholar
• Slater T. F., Sawyer B., Strauli V. Studies on succinate‐tetrazolium reductase systems III Points of coupling of four different tetrazolium salts. Biochimica et Biophysica Acta 1963; 77: 383–393
   PubMed Web of Science ®Google Scholar
• Heikkila R. E., Cabbat F. S., Cohen G. In vivo inhibition of superoxide dismutase in mice by diethyldithiocarbamate. Journal of Biological Chemistry 1976; 251: 2182–2185
   PubMed Web of Science ®Google Scholar
• Enger P. A., Kensler T. W. Effects of a biomimetic superoxide dismutase on complete and multistage carcinogenesis in mouse skin. Carcinogenesis 1985; 6: 1167–1172
   PubMed Web of Science ®Google Scholar
• Saez J. C., Kessler J. A., Bennett M. V.L., Spray D. C. Superoxide dismutase protects cultured neurones against death. Proceedings of the National Academy of Science, USA 1987; 84: 3056–3059
   PubMed Web of Science ®Google Scholar
• Beckman J. S., Minor R. L., White C. W., Repine J. E., Rosen G. M., Freeman B. A. Superoxide dismutase and catalase conjugated to polyethylene glycol increases endothelial enzyme activity and oxidant resistance. Journal of Biological Chemistry 1988; 263: 6884–6892
   PubMed Web of Science ®Google Scholar
• Kyle M. E., Nakae D., Sakaida I., Miccadei S., Farber J. L. Endocytosis of superoxide dismutase is required in order for the enzyme to protect hepatocytes from cytotoxicity of hydrogen peroxide. Journal of Biological Chemistry 1988; 263: 3784–3789
   PubMedGoogle Scholar
• Li L., Wattiaux‐De Conick S., Wattiaux R. Endocytosis of superoxide dismutase by rat liver. Biochemical and Biophysical Research Communications 1992; 184: 727–732
   PubMedGoogle Scholar
• Chalmers R. A., Kroner H., Palmer G., Scott J. T., Watts R. W.E. A comparative study of the xanthine oxidase inhibitors allopurinol and oxipurinol in man. Journal of Clinical Science 1968; 35: 353–362
   PubMed Web of Science ®Google Scholar
• Halliwell B., Gutteridge J. M.C. Free Radicals in Biology and Medicine2nd Ed. Clarendon Press, Oxford 1989
   Google Scholar
• Ikebuchi Y., Masumoto N., Tasaka K., Koike K., Kasahara K., Miyake A., Tanizawa O. Superoxide anion increases intracellular pH, intracellular free calcium and arachidonate release in human amnion cells. Journal of Biological Chemistry 1991; 266: 13233–132237
   PubMedGoogle Scholar
• Oberley L. W., Oberley T. D. Role of antioxidant enzymes in cell immortalisation and transformation. Molecular and Cellular Biochemistry 1988; 84: 147–153
   PubMed Web of Science ®Google Scholar
• Halliwell B. Superoxide dismutase: a contaminant of bovine catalase. Biochemical Journal 1973; 135: 379–381
   PubMedGoogle Scholar
• Burdon R. H., Gill V., Rice‐Evans C. Active oxygen species in the promotion and suppression of tumour cell growth. Oxidative Damage and Repair, K. J.A. Davis. Pergamon Press, Oxford 1992; 791–795
   Google Scholar
• Shibanuma M., Kuroki T., Nose K. Induction of DNA replication and expression of proto‐oncogene c‐myc and c‐fos in quiescent Balb/3T3 cells by xanthine‐xanthine oxidase. Oncogene 1988; 3: 17–21
   Web of Science ®Google Scholar
• Amstad P. A., Krupitza G., Cerutti P. Mechanism of c‐fos induction by active oxygen. Cancer Research 1992; 52: 3952–3960
   PubMed Web of Science ®Google Scholar
• Gopalakrishna R., Anderson W. B. Ca2+ and phospholipid‐independent activation of protein kinase C by selective oxidative modification of the regulatory domain. Proceedings of the National Academy of science, USA 1989; 86: 6758–6762
   PubMed Web of Science ®Google Scholar
• Buskin A. R., Alkalay I., Ben‐Neriah Y. Redox regulation of a protein kinase in the endoplasmic reticulum. Cell 1991; 66: 685–696
   PubMed Web of Science ®Google Scholar
• Schreck R., Reiber P., Baeuerle P. A. Reactive oxygen intermediates as apparently widely used messengers in the activation of the NF‐Kappa B transcription factor and HIV‐1. EMBO Journal 1990; 10: 2247–2258
   Google Scholar
• Abate C., Patel L., Rauscher F. J., Curran T. Redox regulation of Fos + Jun DNA binding activity in vitro. Science 1990; 249: 1157–1161
   PubMed Web of Science ®Google Scholar
• Toledano M., Leonard W. J. Modification of transcription factor NF‐KB binding activity by oxidation/reduction in vitro. Proceedings of the National Academy of Science, USA 1991; 88: 4543–4547
   PubMedGoogle Scholar
• Baeuerle P. A., Schreck R. A role of reactive oxygen intermediates in the activation of the transcription factor NF‐kappa B. Biological Chemistry Hoppe‐Seyler 1992; 373: 740
   Google Scholar
• Wasylyk C., Wasylyk B. Oncogenic conversion of Ets affects redox regulation in vivo and in vitro. Nucleic Acids Research 1993; 21: 523–529
   PubMedGoogle Scholar