Abstract
Oxidants may be natural carcinogens and contribute to several stages of malignant transformation. Active oxygen released by inflammatory phagocytes may induce mutations in protooncogenes and tumor suppressor genes in neighbouring target cells. In addition, oxidants can promote cell growth. Like polypetide growth factors they activate kinases. Because they break DNA, they also induce the poly ADP-ribosylation of chromosomal proteins. Both phosphorylation and poly ADP-ribosylation appear to participate in the transcriptional induction of the growth-related protooncogene c-fos. Growth stimulation by oxidants is modulated by the cellular antioxidant defenses. Maximal growth promotion is observed when cells are protected from excessive toxicity but still maintain a sufficient oxidant signal for the induction of growth-competence genes.
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Cerutti, P., Amstad, P. (1993). Inflammation and Oxidative Stress in Carcinogenesis. In: Nigam, S., Honn, K.V., Marnett, L.J., Walden, T.L. (eds) Eicosanoids and Other Bioactive Lipids in Cancer, Inflammation and Radiation Injury. Developments in Oncology, vol 71. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-3520-1_75
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DOI: https://doi.org/10.1007/978-1-4615-3520-1_75
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