Involvement of Oxygen Free Radicals in Ischaemia-Reperfusion Injury to Murine Turnours: Role of Nitric Oxide

References

• Yoshikawa T., Kokura S., Oyamada H., Iinuma S., Nishimura S., Kaneko T., Naito Y., Kondo M. Anti-tumour effect of ischaemia-reperfusion injury induced by transient embolisation. Cancer Research 1994; 54: 5033–5035
   PubMedGoogle Scholar
• Yoshikawa T., Kokura S., Tainaka K., Naito Y., Kondo M. A novel cancer therapy based on oxygen radicals. Cancer Research 1995; 55: 1617–1620
   PubMed Web of Science ®Google Scholar
• Parkins C. S., Dennis M. E., Stratford M. R. L., Hill S. A., Chaplin D. J. Ischaemia reperfusion injury in tumours: The role of oxygen radicals and nitric oxide. Cancer Research 1995; 55: 6026–4029
   PubMedGoogle Scholar
• Chaplin D. J., Hill S. A. Temporal heterogeneity in microregional erythrocyte flux in experimental solid tumours. British Journal of Cancer 1995; 71: 1210–1213
   PubMed Web of Science ®Google Scholar
• Hill S. A., Pigott K. H., Saunders M. I., Powell M. E. B., Arnold S., Obeid A., Ward G., Leahy M., Hoskin P. J., Chaplin D. J. Microregional blood flow in murine and human tumours assessed using laser Doppler microprobes. British Journal of Cancer 1996; 74(suppl. XXVII)S260–S263
   Google Scholar
• Parks D. A., Granger D. N. Ischaemia-induced vascular changes: role of xanthine oxidase and hydroxyl radicals. American Journal of Physiology 1983; 245: G285
   PubMed Web of Science ®Google Scholar
• Bulkley G. B. Free radicals and other reactive oxygen metabolites: clinical relevance and the therapeutic efficacy of antioxidant therapy. Surgery 1993; 113: 479–483
   PubMed Web of Science ®Google Scholar
• Zimrnerman B. J., Landeneau F. E., Granger D. N. The role of neutrophils in reperfusion injury. Molecular Basis of Oxidative Damage by Leukocytes. CRC Press, Boca RatonUSA 1992; 163–169
   Google Scholar
• Haber F., Weiss J. The catalytic decomposition of hydrogen peroxide by iron salts. Proceedings of the Royal Society of London A 1934; 147: 332–351
   Google Scholar
• Halliwell B., Gutteridge J. M. C. Free Radicals in Biology and Medicinesecond edition. Oxford University Press, OxfordUK 1989
   Google Scholar
• Kukreja R. C., Hess M. L. Oxygen radicals, neutrophil-derived oxidants, and myocardial reperfusion injury. Pathophysiology of Reperfusion Injury. CRC Press, FloridaUSA 1993
   Google Scholar
• McMillen M. A., Huribal M., Sumpio B. Common pathway of endothelial-leukocyte interaction in shock, ischaemia, and reperfusion. American Journal of Surgey 1993; 166: 557–562
   PubMed Web of Science ®Google Scholar
• Wardman P., Candeias L. P. Fenton chemistry; an introduction. Radiation Research 1996; 145: 523–531
   PubMed Web of Science ®Google Scholar
• Parkins C. S., Hill S. A., Stratford M. R. L., Dennis M. F., Stubbs M., Chaplin D. J. The relationship between extracellular lactate and tumour pH in a murine tumour model of ischaemia-reperfusion injury. British Journal of Cancer 1997a; 75(3)319–323
   PubMed Web of Science ®Google Scholar
• Coyle J. T., Puttfarcken P. Oxidative stress, glutamate, and neurodegenerative disorders. Science 1993; 262: 689–695
   PubMed Web of Science ®Google Scholar
• Beal M. F. Oxidative damage in neurodegenerative diseases. The Neuroscientist 1997; 3(1)21–27
   Web of Science ®Google Scholar
• Shoji Y., Uedono Y., Ishikura H., Takeyama N., Tanaka T. DNA damage induced by tumour necrosis factor-α in L929 cells is mediated by mitochon-drial oxygen radical formation. Immunology 1995; 84: 543–548
   PubMed Web of Science ®Google Scholar
• Meier B., Radeke H. H., Selle S., Younes M., Sies H., Resch K., Habermehl G. G. Human fibro-blasts release reactive oxygen species in response to interleukin-1 or tumour necrosis factor-α. Biochemical Journal 7989; 263: 539–545
   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
• Durak I., Isik Umit A. C., Canbolat O., Akyol O., Kavutcu M. Adenosine deaminase, 5′ nucleoti-dase, xanthine oxidase, superoxide dismutase, and catalase activities in cancerous and noncancerous human laryngeal tissues. Free Radicals in Biology and Medicine 1993; 15: 681–484
   PubMed Web of Science ®Google Scholar
• Durak I., Perk H., Kavutcu M., Canbolat O., Akyol O., Beduk Y. Adenosine deaminase, 5′ nucleo-tidase, xanthine oxidase, superoxide dismutase, and catalase activities in cancerous and noncancerous human bladder tissues. Free Radicals in Biology and Medicine 1994; 16: 825–831
   PubMed Web of Science ®Google Scholar
• Okamoto K., Toyokuni S., Uchida K., Ogawa O., Takenewa J., Kakehi Y., Kinoshita H., Hattori-Nakakuki Y., Hiai H., Yoshida O. Formation of 8-hydroxy-2′-deoxyguanosine and 4-hydroxy-2-nonenal-modified proteins in human renal-cell carcinoma. International Journal of Cancer 1994; 58: 825–829
   PubMed Web of Science ®Google Scholar
• Oberley L. W., Oberley T. D. Reactive oxygen species in the etiology of cancer. Drugs, Diet and Disease. 1. Harwood, London 1995; 47–63
   Google Scholar
• Oberley L. W., Oberley T. D. Antioxidant enzyme levels in cancer. Histology and Histopathology 1997; 12: 525–535
   PubMed Web of Science ®Google Scholar
• Toyokuni S., Okamoto K., Yodoi J., Hiai H. Persistent oxidative stress in cancer. FEBS Letters 1995; 358
   Web of Science ®Google Scholar
• Rice-Evans C. A., Bplock A. T. Current status of antioxidant therapy. Free Radicals in Biology and Medicine 1993; 15: 7–96
   Web of Science ®Google Scholar
• Ben-Yoseph O., Ross B. D. Oxidation therapy: the use of a reactive oxygen species-generating enzyme system for tumour treatment. British Journal of Cancer 1994; 70: 1131–1135
   PubMed Web of Science ®Google Scholar
• Candeias L. P., Folkes L. K., Wardman P. Amplification of oxidative stress by decarboxylation: a new strategy in anti-tumour drug design. Biochemical Society Transactions 1995; 23: 262S
   PubMed Web of Science ®Google Scholar
• Rojas A. Carbogen and nicotinamide as tumour radiosensitizers. Radiation Research 1985–1995. Taylor & Francis, UK 1996; Vol. 2: 783–786
   Google Scholar
• von Sonntag C. The Chemical Basis of Radiation Biology. Taylor & Francis, London 1987
   Google Scholar
• Parkins C. S., Hill S. A., Stratford M. R. L., Dennis M. F., Chaplin D. J. Metabolic and clonogenic consequences of ischaemia-reperfusion insult in solid tumours. Experimental Physiology 1997b; 82: 361–368
   PubMed Web of Science ®Google Scholar
• Kirschner R. E., Fantini G. A. Role of iron and oxygen-derived free radicals in ischaemia-reperfusion injury. Journal of the American College of Surgery 1994; 179: 103–117
   PubMed Web of Science ®Google Scholar
• Anderson R. F., Patel K. B., Reghebi K., Hill S. A. Conversion of xanthine dehydrogenase to xanthine oxidase as a possible marker for hypoxia in tumours and normal tissues. British Journal of Cancer 1989; 60: 193–197
   PubMed Web of Science ®Google Scholar
• Furchgott R. F., Zawadzki J. V. The obligatory role of endothelial cells in the relaxation of arterial smooth muscle by acetylcholine. Nature (London) 1980; 28: 687–692
   Google Scholar
• Moncada S., Palmer R. M. J., Higgs E. A. Nitric oxide: Physiology, pathophysiology and pharmacology. Pharmacology Reviews 1991; 43(2)109–142
   PubMed Web of Science ®Google Scholar
• Kubes P., Suzuki M., Granger D. N. Nitric oxide: An endogenous modulator of leukocyte adhesion. Proceedings of the National Academy of Sciences, USA 1991; 88: 4651–4655
   PubMed Web of Science ®Google Scholar
• Siegfried M. R., Erhardt J., Rider T., Ma X.-L., Lefer A. M. Cardioprotection and alteration of endotheiial dysfunction by organic nitric oxide donors in myocardial ischaemia-reperfusion. Journal of Pharmacology and Experimental Therapeutics 1992; 260: 668–475
   PubMed Web of Science ®Google Scholar
• Knox L. K., Stewart A. G., Hayward P. G., Morrison W. A. Nitric oxide synthase inhibitors improve skin flap survival in the rat. Microsurgery 1994; 15: 708–711
   PubMed Web of Science ®Google Scholar
• Matheis G., Sherman M. P., Buckberg G. D., Haybron D. M., Young H. H., Ignarro L. J. Role of L-arginine-nitric oxide pathway in myocardial reoxy-genation injury. American Journal of Physiology 1992; 262: H616–H620
   PubMed Web of Science ®Google Scholar
• Darley-Usmar V., Wiseman H., Halliwell B. Nitric oxide and oxygen radicals: a question of balance. FEBS. Letters 1995; 369: 131–135
   Google Scholar
• Korbelik M. K. The role of nitric oxide in the response of solid tumors to photodynamic therapy. Photochemistry and Photobiology 1997; 65: 555
   Google Scholar
• Wink D. A., Hanbauer I., Krishna M. C., DeGraff W., Gamson J., Mitchell J. B. Nitric oxide protects against cellular damage and cytotoxicity from reactive oxygen species. Proceedings of the National Academy of Sciences of the USA 1993; 90: 9813–9817
   PubMed Web of Science ®Google Scholar
• Floyd R. A., Watson J. J., Wong P. K. Sensitive assay of hydroxyl free radical formation utilising high performance liquid chromatography with electrochemical detection of phenol and salicylate hydmxylation products. Journal of Biochemical and Biophysical Methods 1984; 10: 221–235
   PubMedGoogle Scholar
• Powell S. R., Hall D. Use of salicylate as a probe for OH formation in isolated ischaemic rat hearts. Free Radicals in Biology and Medicine 1990; 9: 133–141
   PubMed Web of Science ®Google Scholar
• Rose S., Floyd R. A., Eneff K., Buhren V., Massion W. Intestinal ischaemia: Reperfusion-mediated increase in hydroxyl free radical formation as reported by salicylate hydroxylation. Shock 1994; 1(6)452–456
   PubMed Web of Science ®Google Scholar
• Halliwell B., Kaur H., Ingelman-Sundberg M. Hydroxylation of salicylate as an assay for hydroxyl radicals: A cautionary note. Free Radical Biology and Medicine 1991; 10: 439–441
   PubMed Web of Science ®Google Scholar
• Montgomery J., Ste-Marie L., Boismenu D., Vachon L. Hydroxylation of aromatic compounds as indices of hydroxyl radical production: a cautionary note revisited. Free Radical Biology and Medicine 1995; 19: 927–933
   PubMed Web of Science ®Google Scholar
• Narayan M., Berliner L. J., Merola A. J., Diaz P. T., Clanton T. L. Biological reactions of peroxynitrite: Evidence for an alternative pathway of salicylate hydroxylation. Free Radical Research 1997; 27: 63–72
   PubMed Web of Science ®Google Scholar
• Halliwell B., Kaur H. Hydroxylation of salicylate and phenylalanine as assays for hydroxyl radicals: a cautionary note visited for the third time. Free Radical Research 1997; 27: 239–244
   PubMed Web of Science ®Google Scholar
• Hammer B., Parker W. D., Bennett J. P. NMDA receptors increase OH radicals in vivo by using nitric oxide synthase and protein kinase C. NeuroReport 1993; 5: 72–74
   PubMed Web of Science ®Google Scholar
• Parkins C. S., Hill S. A., Lonergan S. J., Horsman M. R., Chadwick J. A., Chaplin D. J. Ischaemia induced cell death in tumors: importance of temperature and pH. International Journal of Radiation Oncology Biology and Physics 1994; 29: 499–503
   PubMed Web of Science ®Google Scholar
• Li L., Lau B. H. A simplified in vitro model of oxidant injury using vascular endothelial cells. In vitro Cell and Developmental Biology 1993; 29A(7)531–536
   Web of Science ®Google Scholar
• Tan S., Yokoyama Y., Dickens E., Cash T. G., Freeman B. A., Parks D. A. Xanthine oxidase activity in the circulation of rats following haemorrhagic shock. Free Radicals in Biology and Medicine 1993; 15(4)407–414
   PubMed Web of Science ®Google Scholar
• Block E. R. Hydrogen peroxide alters the physical state and function of the plasma membrane of pulmonary artery endothelial cells. Journal of Cellular Physiology 1991; 146: 362–369
   PubMed Web of Science ®Google Scholar
• Oberley L. W., Leuthauser S. W. H. C., Buettner G. R., Sorenson J. R. J., Oberley T. D., Bize I. B. The use of superoxide dismutase in the treatment of cancer. Pathology of Oxygen. Academic Press, New York 1982; 207–218
   Google Scholar
• Thomsen L. L., Lawton F. G., Knowles R. G., Beesley J. E., Riveros-Moreno V., Moncada S. Nitric oxide synthase activity in human gynecological cancer. Cancer Research 1994; 54: 1352–1354
   PubMed Web of Science ®Google Scholar
• Thomsen L. L., Miles D. W., Happerfield L., Bobrow L. G., Knowles R. G., Moncada S. Nitric oxide synthase activity in human breast cancer. British Journal of Cancer 1995; 72: 41–44
   PubMed Web of Science ®Google Scholar
• McCabe D. R., Maher T. J., Acworth I. N. Improved method for the estimation of hydroxyl free radical levels in vivo based on liquid chromatography with electrochemical detection. Journal of Chromatography B 1997; 691: 23–32
   PubMed Web of Science ®Google Scholar
• Beckman J. S., Beckman T. W., Chen J., Marshall P. A., Freeman B. A. Apparent hydroxyl radical production by peroxynitrite: Implications for endothelial injury from nitric oxide and superoxide. Proceedings National Academy of Sciences USA 1990; 87: 1620–1624
   PubMed Web of Science ®Google Scholar
• Villa L. M., Salas E., Darley-Usmar V. M., Radomski M. W., Moncada S. Peroxynitrite induces both vasodilatation and impaired vascular relaxation in the isolated perfused rat heart. Proceeding of the National Academy of Sciences of the USA 1994; 91: 12383–12387
   PubMed Web of Science ®Google Scholar
• Iha S., Orita K., Kanno T., Utsumi T., Sato E., Inoue M., Utsumi K. Oxygen-dependent inhibition of neutrophil respiratory burst by nitric oxide. Free Radical Research 1996; 25(6)489–498
   PubMed Web of Science ®Google Scholar
• Parkins C. S., Holder A. L., Dennis M. F., Stratford M. R. L., Hill S. A., Chaplin D. J. Tumour cytotoxicity following ischaemia-reperfusion injury: role of neutrophil infiltration and oxidative stress. International Journal of Radiation Oncology Biology and Physics 1998, in press
   Google Scholar