scholarly journals Genetic Toxicity Assessment: Employing the Best Science for Human Safety Evaluation Part II: Performances of the In Vitro Micronucleus Test Compared to the Mouse Lymphoma Assay and the In Vitro Chromosome Aberration Assay

2006 ◽  
Vol 96 (2) ◽  
pp. 214-217 ◽  
Author(s):  
Elisabeth Lorge ◽  
Carine Lambert ◽  
Véronique Gervais ◽  
Nathalie Becourt-Lhote ◽  
Jean-Luc Delongeas ◽  
...  
Keyword(s):  
Chromosome Aberration ◽  
Micronucleus Test ◽  
Safety Evaluation ◽  
Toxicity Assessment ◽  
Genetic Toxicity ◽  
Human Safety ◽  
Chromosome Aberration Assay ◽  
Mouse Lymphoma Assay ◽  
Mouse Lymphoma

scholarly journals Genetic Toxicity Assessment: Employing the Best Science for Human Safety Evaluation

2006 ◽  
Vol 96 (1) ◽  
pp. 1-1 ◽  
Author(s):  
J. I. Goodman ◽  
B. Gollapudi ◽  
L. D. Lehman-McKeeman
Keyword(s):  
Safety Evaluation ◽  
Toxicity Assessment ◽  
Genetic Toxicity ◽  
Human Safety

Genotoxicity Studies on Sel-Plex®, a Standardized, Registered High-Selenium Yeast

2006 ◽  
Vol 25 (6) ◽  
pp. 477-485 ◽  
Author(s):  
James C. Griffiths ◽  
Ray A. Matulka ◽  
Ronan Power
Keyword(s):  
Chromosome Aberration ◽  
Micronucleus Test ◽  
Mutagenic Activity ◽  
Human Lymphocytes ◽  
Selenium Yeast ◽  
Yeast Saccharomyces Cerevisiae ◽  
Reverse Mutation ◽  
High Selenium ◽  
Chromosome Aberration Test

Selenium, recognized as an essential nutrient for human health, is a component of proteins and enzymes required for various biological functions and is currently being used as a feed supplement for livestock in geographical areas that are naturally low in selenium. Selenium is structurally similar to sulfur, replacing the sulfur atom in stoichiometric amounts and thus functions through an association with proteins, termed selenoproteins. In geographic areas low in selenium, there is the potential for animals (including humans) to become selenium deficient and this potential deficiency can be remedied by consumption of exogenous selenium, including selenium-enriched yeast ( Saccharomyces cerevisiae) that contains high levels of organic selenium (e.g., selenized yeast). A unique, standardized, registered high selenium food-grade baker’s yeast ( S. cerevisiae; Sel-Plex®), was tested in the following battery of Genotoxicity assays; (1) a bacterial reverse mutation test (Ames test); (2) an in vitro mammalian chromosome aberration test; and (3) a mouse micronucleus test. Under the conditions of this assay, Sel-Plex® showed no evidence of mutagenic activity in Salmonella typhimurium, in the bacterial reverse mutation test. Sel-Plex® did not induce significant chromosomal aberrations in cultured human lymphocytes in the in vitro mammalian chromosome aberration test. Sel-Plex® did not statistically increase the frequency or proportion of micronucleated immature erythrocytes in the mouse micronucleus test. Thus, from the studies presented here, the authors conclude that Sel-Plex® is nongenotoxic.

scholarly journals Assessment of Cyto/Genotoxicity of Irinotecan in V79 Cells Using the Comet, Micronucleus, and Chromosome Aberration Assay

2010 ◽  
Vol 61 (1) ◽  
pp. 1-9 ◽  
Author(s):  
Vilena Kašuba ◽  
Ružica Rozgaj ◽  
Marija Gamulin ◽  
Ivančica Trošić
Keyword(s):  
Comet Assay ◽  
Chromosome Aberration ◽  
Topoisomerase I ◽  
Micronucleus Test ◽  
Statistical Significance ◽  
Time Dependent ◽  
V79 Cells ◽  
Chromosome Aberration Assay ◽  
Dependent Relation ◽  
Dose Dependent

Assessment of Cyto/Genotoxicity of Irinotecan in V79 Cells Using the Comet, Micronucleus, and Chromosome Aberration AssayIrinotecan is a topoisomerase I interactive agent, widely used in the treatment of metastatic colorectal cancer. The genotoxic effects of the maximum single dose (18 μg mL-1), recommended monotherapy dose (9 μg mL-1), and recommended combined therapy dose (4.5 μg mL-1) of irinotecan were studied on V79 cells using the comet assay, chromosome aberration assay, and micronucleus test. The cells were treated with irinotecan for 2 h or 24 h. The statistical significance of the results was determined using the one-way ANOVA test and a nonparametric Mann Whitney U test. The comet assay did not show dose-dependent or time-dependent effects. The chromosome aberration analysis showed large DNA rearrangements, i.e., chromosome exchanges. Although the exposed cultures showed a significant increase in micronucleated cells in respect to control, no dose-dependent relation was established among the treated cultures. Time-dependent effect was also not observed.

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