Hyperthermic sensitization by the radical initiator 2,2′-azobis (2-amidinopropane) dihydrochloride (AAPH). I. In vitro studies

References

• Buettner G. R. Spin trapping: ESR parameters of spin adducts. Free Radical Biology Medicine 1987; 3: 259–303
   PubMed Web of Science ®Google Scholar
• Da Silva V. F., Feeley M., Raaphorst G. P. Hyperthermic potentiation of BCNU toxicity in BCNU-resistant human glioma cells. Journal of Neurooncology 1991; 11: 37–41
   PubMed Web of Science ®Google Scholar
• Dooley M. M., Sano N., Kawashima H., Nakamura T. Effects of 2,2′-azobis(2-amidinopropane) hydrochloride in vivo and protection by vitamin E. Free Radical Biology Medicine 1990; 9: 199–204
   PubMed Web of Science ®Google Scholar
• Freeman M. L., Malcolm A. W., Meredith M. J. Role of glutathione in cell survival after hyperthermic treatment of Chinese hamster ovary cells. Cancer Research 1985; 45: 6308–6313
   PubMed Web of Science ®Google Scholar
• Gerweck L. E., Nygaard T. G., Burlett M. Response of cells to hyperthermia under acute and chronic hypoxic conditions. Cancer Research 1979; 39: 966–972
   PubMed Web of Science ®Google Scholar
• Halliwell B., Gutteridge J. M. C. Free Radicals in Biology and Medicine. Clarendon, Oxford 1989
   Google Scholar
• Issels R. D., Mittermuller J., Gerl A., Simon W., Oortmaier A., Denzlinger C., Sauer H., Wilmanns W. Improvement of local control by regional hyperthermia combined with systemic chemotherapy (ifosfamide plus etoposide) in advanced sarcomas: updated report on 65 patients. Journal of Cancer Research and Clinical Oncology 1991; 117: S141–147
   PubMed Web of Science ®Google Scholar
• Kagan V. E., Tsuchiya M., Serbinova E., Packer L., Sies H. Interaction of the pyridoindole stobadine with peroxyl, superoxide and chromanoxyl radicals. Biochemical Pharmacology 1993; 45: 393–400
   PubMed Web of Science ®Google Scholar
• Kapp D. S., Barnett T. A., Cox R. S., Lee E. R., Lohrbach A., Fessenden P. Hyperthermia and radiation therapy of local-regional recurrent breast cancer: prognostic factors for response and local control of diffuse or nodular tumours. International Journal of Radiation Oncology, Biology and Physics 1991; 20: 1147–1164
   PubMed Web of Science ®Google Scholar
• Kim S. H., Kim J. H., Afieri A. A., He S. Q., Young C. W. Gossypol, a hyperthermic sensitizer of HeLa cells. Cancer Research 1985; 45: 6338–6340
   PubMed Web of Science ®Google Scholar
• Laskowitz D. T., Elion G. B., Dewhirst M. W., Griffith O. W., Savina P. M., Blum M. R., Prescott D. M., Bigner D. D., Friedman H. S. Hyperthermia-induced enhancement of melphalan activity against a melphalan-resistant human rhabdomyosarcoma xenograft. Radiation Research 1992; 129: 218–223
   PubMed Web of Science ®Google Scholar
• Lin P. S., Kwock L., Butterfield C. E. Diethyldithiocarbamate enhancement of radiation and hyperthermic effects on Chinese hamster cells in vitro. Radiation Research 1979; 77: 501–511
   PubMed Web of Science ®Google Scholar
• Loven D. P., Leeper D. B., Oberley L. W. Superoxide dismutase levels in Chinese hamster ovary cells and ovarian carcinoma cells after hyperthermia or exposure to cycloheximide. Cancer Research 1985; 45: 3029–3033
   PubMed Web of Science ®Google Scholar
• Mitchell J. B., Russo A. Thiols, thiol depletion, and thermosensitivity. Radiation Research 1983; 95: 471–485
   PubMed Web of Science ®Google Scholar
• Mitchell J. B., Russo A., Kinsella T. J., Glatstein E. Glutathione elevation during thermotolerance induction and thermosensitization by glutathione depletion. Cancer Research 1983; 43: 987–991
   PubMed Web of Science ®Google Scholar
• Morrow M., Hager C., Berger D., Djordjevic B. Chloroquine as a hyperthermia potentiator. Journal of Surgery Research 1989; 46: 637–639
   PubMed Web of Science ®Google Scholar
• Niki E. Free radical initiators as a source of water- or lipid-soluble peroxyl radicals. Methods of Enzymology 1990; 186B: 100–108
   Google Scholar
• Niki E., Komuro E., Takahashi M., Urano S., Ito E., Terao K. Oxidative hemolysis of erythrocytes and its inhibition by free radical scavengers. Journal of Biological Chemistry 1988; 263: 19809–19814
   PubMed Web of Science ®Google Scholar
• Oleson J. R., Samulski T. V., Leopold K. A., Clegg S. T., Dewhirst M. W., Dodge R. K., George S. L. Sensitivity of hyperthermia trial outcomes to temperature and time: implications for thermal goals of treatment. International Journal of Radiation Oncology, Biology and Physics 1993; 25: 289–297
   PubMed Web of Science ®Google Scholar
• Overgaard J. The current and potential role of hyperthermia in radiotherapy. International Journal of Radiation Oncology, Biology and Physics 1989; 16: 535–549
   PubMed Web of Science ®Google Scholar
• Palozza P., Moualla S., Krinksky N. I. Effects of beta-carotene and alpha-tocopherol on radical-initiated peroxidation of microsomes. Free Radical Biology and Medicine 1992; 13: 127–136
   PubMed Web of Science ®Google Scholar
• Russo A., Mitchell J. B., Finkelstein E., Degraff W. G., Spiro I. J., Gamson J. The effects of cellular glutathione elevation on the oxygen enhancement ratio. Radiation Research 1985; 103: 232–239
   PubMed Web of Science ®Google Scholar
• Russo A., Mitchell J. B., McPherson S. The effects of glutathione depletion on thermotolerance and heat stress protein synthesis. British Journal of Cancer 1984; 49: 753–758
   PubMed Web of Science ®Google Scholar
• Shimasaki H., Saypil W. H., Ueta N. Free radical-induced liver injury. II. Effects of intraperitoneally administered 2,2′-azobis(2-amidinopropane) dihydrochloride on the fatty acid profiles of hepatic triacylglycerol and phospholipids. Free Radical Research Communication 1991; 14: 247–252
   PubMed Web of Science ®Google Scholar
• Shinohara K., Kawakami N., Kugotani M., Nakano H. Gallium citrate, a new sensitizer of cells to hyperthermia. Japanese Journal of Cancer 1988; 79: 21–23
   PubMedGoogle Scholar
• Spitz D. R., Dewey W. C., Li G. C. Hydrogen peroxide or heat shock induces resistance to hydrogen peroxide in Chinese hamster fibroblasts. Journal of Cell Physiology 1987; 131: 364–373
   PubMed Web of Science ®Google Scholar
• Terao K., Niki E. Damage to biological tissues induced by radical initiator 2,2′-azobis(2-amidinopropane) dihydrochloride and its inhibition by chain-breaking antioxidants. Free Radical Biology and Medicine 1986; 2: 193–201
   Google Scholar
• von Sonntag C. The Chemical Basis of Radiation Biology. Taylor & Francis, London 1987
   Google Scholar
• Weishaupt K. R., Gomer C. J., Dougherty T. J. Identification of singlet oxygen as the cytotoxic agent in photo-inactivation of a murine tumor. Cancer Research 1976; 36: 2326–2329
   PubMed Web of Science ®Google Scholar