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. 1983 Sep;51:223–226. doi: 10.1289/ehp.8351223

In vitro toxicity and transformation potency of nickel compounds.

K Hansen, R M Stern
PMCID: PMC1569296  PMID: 6641656

Abstract

An in vitro bioassay utilizing BHK-21 cells in culture is used to determine the relative transformation potential of a number of nickel compounds including, as relatively insoluble particulates a known carcinogen (Ni3S2) and several oxides either of commercial interest or found in the working environment in the metal industry (e.g., NiO), and a soluble salt [Ni(CH3COO)2]. Although a wide range of transformation potency is found as a function of the dose of Ni per area of culture, all substances produce the same number of transformed colonies at the same degree of toxicity (e.g., 50% survival). If toxicity is a direct measure of intracellular concentration, then apparently nickel per se is the ultimate transforming agent independent of source or uptake mechanism.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Costa M., Abbracchio M. P., Simmons-Hansen J. Factors influencing the phagocytosis, neoplastic transformation, and cytotoxicity of particulate nickel compounds in tissue culture systems. Toxicol Appl Pharmacol. 1981 Sep 15;60(2):313–323. doi: 10.1016/0041-008x(91)90234-6. [DOI] [PubMed] [Google Scholar]
  2. Kuehn K., Sunderman F. W., Jr Dissolution half-times of nickel compounds in water, rat serum, and renal cytosol. J Inorg Biochem. 1982 Aug;17(1):29–39. doi: 10.1016/s0162-0134(00)80227-5. [DOI] [PubMed] [Google Scholar]
  3. Oskarsson A., Andersson Y., Tjälve H. Fate of nickel subsulfide during carcinogenesis studied by autoradiography and X-ray powder diffraction. Cancer Res. 1979 Oct;39(10):4175–4182. [PubMed] [Google Scholar]
  4. Rivedal E., Sanner T. Metal salts as promoters of in vitro morphological transformation of hamster embryo cells initiated by benzo(a)pyrene. Cancer Res. 1981 Jul;41(7):2950–2953. [PubMed] [Google Scholar]
  5. Saxholm H. J., Reith A., Brøgger A. Oncogenic transformation and cell lysis in C3H/10T 1/2 cells and increased sister chromatid exchange in human lymphocytes by nickel subsulfide. Cancer Res. 1981 Oct;41(10):4136–4139. [PubMed] [Google Scholar]
  6. Stern R. M., Pigott G. H. In vitro RPM fibrogenic potential assay of welding fumes. Environ Health Perspect. 1983 Sep;51:231–236. doi: 10.1289/ehp.8351231. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Styles J. A. A method for detecting carcinogenic organic chemicals using mammalian cells in culture. Br J Cancer. 1977 Nov;36(5):558–563. doi: 10.1038/bjc.1977.231. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Sunderman F. W., Jr Recent research on nickel carcinogenesis. Environ Health Perspect. 1981 Aug;40:131–141. doi: 10.1289/ehp.8140131. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Weinzierl S. M., Webb M. Interaction of carcinogenic metals with tissue and body fluids. Br J Cancer. 1972 Aug;26(4):279–291. doi: 10.1038/bjc.1972.38. [DOI] [PMC free article] [PubMed] [Google Scholar]

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