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PMID: 8937893 Published · ppublish English Journal Article

Use of the Syrian hamster embryo cell transformation assay for determining the carcinogenic potential of heavy metal compounds.

Fundamental and applied toxicology : official journal of the Society of Toxicology ·Vol. 34 ·No. 1 ·1996-11-00 ·Pages 67-72

Kerckaert GA, LeBoeuf RA, Isfort RJ

Abstract

Cobalt sulfate hydrate, gallium arsenide, molybdenum trioxide, vanadium pentoxide, and nickel sulfate heptahydrate were tested in the Syrian hamster embryo (SHE) assay in order to increase the SHE assay database for heavy metals. All five compounds produced significant morphological transformation at one or more doses in a dose-responsive manner. Cobalt sulfate hydrate, gallium arsenide, molybdenum trioxide, and nickel (II) sulfate heptahydrate were all positive with a 24-hr exposure, suggesting direct DNA perturbation. Vanadium pentoxide was negative with a 24-hr exposure, but positive with a 7-day exposure. This pattern of response (24-hr SHE negative/7-day SHE positive) has been seen with other chemicals which have tumor promotion-like characteristics. Since the inception of the use of the SHE cell transformation assay for detecting the neoplastic transformation potential of chemicals, over 42 heavy metal compounds have been tested in this assay. Based on the 24 metal compounds which have been tested in the SHE, Salmonella, and some type of rodent bioassay, the SHE assay is 92% concordant with rodent bioassay carcinogenicity results, including a sensitivity of 95% (21/22) and a specificity of 50% (1/2). At this time, the measure of SHE assay specificity for rodent carcinogenicity of metals is limited by the paucity of metal compounds which are rodent noncarcinogens. The Salmonella assay results are only 33% concordant with the rodent bioassay for these same chemicals. This relatively high concordance between the SHE assay and the rodent bioassay carcinogenicity results demonstrates the utility of the SHE assay for determining the carcinogenic potential of heavy metal compounds in rodent cancer bioassays.

MeSH Terms
Animals Carcinogens/toxicity Cell Transformation, Neoplastic Cells, Cultured Cricetinae Culture Media Embryo, Mammalian/cytology,drug effects Mesocricetus Metals/toxicity
Chemicals
Carcinogens Culture Media Metals
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Kerckaert G A
Corporate Professional & Regulatory Services, Procter & Gamble Company, Miami Valley Laboratories, Cincinnati, Ohio 45253-8707, USA.
LeBoeuf R A
Isfort R J
Article Info
Journal
Fundamental and applied toxicology : official journal of the Society of Toxicology
Abbr.
Fundam Appl Toxicol
ISSN
0272-0590
Published
1996-11-00
Pages
67-72
Language
English
Region
United States
NLM ID
8200838
Subset
IM
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