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Metals and Anticancer Drug Resistance

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Part of the book series: Handbook of Experimental Pharmacology ((HEP,volume 115))

Abstract

Metals have historically held a distinguished position in the Pharmacopeia. Metals, such as mercury and arsenic, were the mainstays of early physicians (WOod 1877). Today more than 80 of the known metals in the periodic table have been shown to have biological activity. Most, however, are toxic and do not have desirable therapeutic activity. Exceptions include aluminum, bismuth, gold, lithium, and platinum. Aluminum is used as an antacid, while bismuth finds employment for gastrointestinal disturbances. Gold salts are still useful for the treatment of rheumatism and lithium has become an important treatment for depression. Metals, such as zinc and iron, are also important as nutritional supplements. A number of drugs also require metals for their biological activity. For example, the anticancer agent bleomycin requires iron for its DNA cleaving and antitumor activity (LAzo and SEbti 1989). Metals can also induce gene transcription and alter protein function. Many transcription factors and enzymes require metals.

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© 1995 Springer-Verlag Berlin Heidelberg

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Lazo, J.S. (1995). Metals and Anticancer Drug Resistance. In: Goyer, R.A., Cherian, M.G. (eds) Toxicology of Metals. Handbook of Experimental Pharmacology, vol 115. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-79162-8_12

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  • DOI: https://doi.org/10.1007/978-3-642-79162-8_12

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-79164-2

  • Online ISBN: 978-3-642-79162-8

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