Abstract
Many classes of transition metal complexes enhance cellular radiation damage both in vitro and in vivo. The radiosensitization of hypoxic cells is of clinical relevance due to the inherent radioresistance of a tumor hypoxic fraction. Selective attack on hypoxic cells may also be achieved by development of hypoxic cytotoxins and chemosensitizers, which may act by enhancing the hypoxic toxicity of other agents. In radiosensitization three principal mechanisms by which metal complexes act are by DNA-binding with subsequent consequences to repair processes, thiol depletion, and by an electron-affmic mechanism, implying reduction of the metal complex and subsequent fixation of damage on the intracellular target of radiation, DNA. The types of complexes shown to act by the above mechanisms are summarized.
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Farrell, N. (1989). Metal Complexes as Radiosensitizers. In: Baulieu, E., et al. Ruthenium and Other Non-Platinum Metal Complexes in Cancer Chemotherapy. Progress in Clinical Biochemistry and Medicine, vol 10. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-74760-1_5
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DOI: https://doi.org/10.1007/978-3-642-74760-1_5
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