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PMID: 570089 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Enhancement of viral transformation for evaluation of the carcinogenic or mutagenic potential of inorganic metal salts.

Cancer research ·Vol. 39 ·No. 1 ·1979-01-00 ·Pages 193-8

Casto BC, Meyers J, DiPaolo JA

Abstract

Thirty-eight metal salts were tested for their capacity to enhance transformation of Syrian hamster embryo cells by a simian adenovirus, SA7. All of the metal salts with known carcinogenic potential in animals or mutagenic activity in microbial or mammalian cells increased the SA7 transformation frequency. Metals were classified into three groups according to the concentration necessary to produce significant enhancement. Those showing highest activity (positive at less than 0.05 mM) were the salts of antimony, arsenic, cadmium, chromium, and platinum. The second group (positive from 0.05 to 0.6 mM) included beryllium, cobalt, copper, lead, manganese, mercury, nickel, silver, thallium, and zinc. Iron salts were placed in a third group (only positive at concentrations greater than 0.9 mM). With the exception of ZnCl2 and ZnSO4, enhancement was demonstrated by both a relative increase in the viral transformation frequency and an absolute increase in the number of transformed foci among treated cells. The latter observation and the demonstration of enhancement in the absence of overt cell killing negate the possibility that enhancement resulted from the selection of transformation-sensitive cells.

MeSH Terms
Adenoviruses, Simian Animals Carcinogens Cell Transformation, Viral Cells, Cultured Cricetinae Drug Evaluation, Preclinical/methods Embryo, Mammalian Mesocricetus Metals/pharmacology Mutagens Salts/pharmacology
Chemicals
Carcinogens Metals Mutagens Salts
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Casto B C
Meyers J
DiPaolo J A
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1979-01-00
Pages
193-8
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
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