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In vitro assessment of the toxicity of metal compounds

III. Effects of metals on DNA structure and function in intact cells

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Abstract

A review has been compiled illustrating the directions taken in examining the genotoxic effects of metals and their compounds centering only on those studies pertaining to effects of metals and their compounds on DNA structure and function, such as the induction of DNA strand breaks, production of DNA-protein crosslinks, induction of chromosomal aberrations, and sister chromatid exchanges. Although it is premature to declare a cause and effect relationship between the carcinogenic activity of metals and their ability to induce one or more lesions in DNA, strong evidence is emerging to suggest such a relationship. Low concentrations of metals induce the appearance of DNA lesions, such as strand breaks and crosslinks, or induce sister chromatid exchanges or DNA repair synthesis. Assays based upon these events constitute extremely sensitive probes for genotoxic effects of metals and their compounds. These effects of metals on DNA are consistent with the currently accepted mechanism of chemical carcinogenesis, allowing the acquisition and propagation of altered DNA function. The lack of complete information on the activity of metals in producing DNA lesions allow only preliminary conclusions to be drawn. Certain compounds containing potentially or actually carcinogenic elements, such as Ni, Be, As, Cr, Cd, and to a minor extent Pb, have yielded positive responses in one or more DNA lesion assays. At relatively nontoxic levels of Ni and Cr, considerable evidence suggests that multiple types of DNA lesions are induced.

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Authors and Affiliations

  1. Division of Toxicology, Department of Pharmacology, University of Texas Medical School at Houston, PO Box 20708, 77025, Houston, Texas

    Nelwyn T. Christie & Max Costa

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  1. Nelwyn T. Christie
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  2. Max Costa
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Christie, N.T., Costa, M. In vitro assessment of the toxicity of metal compounds. Biol Trace Elem Res 5, 55–71 (1983). https://doi.org/10.1007/BF02916927

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  • DOI: https://doi.org/10.1007/BF02916927

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