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High Content Screening Analysis to Evaluate the Toxicological Effects of Harmful and Potentially Harmful Constituents (HPHC)
Published on: May 10, 2016
Proposed criteria for specific and non-specific chromosomal genotoxicity based on hydrophobic interactions
Susanne B Dorn1, Gisela H Degen, Tina Müller
1Institut für Arbeitsphysiologie an der Universität Dortmund, Ardeystr. 67, D-44139 Dortmund, Germany.
Abstract:
Tests for chromosomal damage are indispensable in the genotoxicity testing battery. Thus, positive results of clastogenicity or aneugenicity tests are of key relevance in safety assessment and product development. Schultz and Onfelt [N. Schultz, A. Onfelt, Sensitivity of cytokinesis to hydrophobic interactions. Chemical induction of bi- and multi-nucleated cells, Chem. Biol. Interact. 126 (2000) 97-123.] have studied the chemical induction of bi- and multi-nucleated cells in Chinese hamster V79 cells and compared non-specific agents with inducers acting through a known specific mechanism. They separated compounds with a specific action from those with a non-specific action based on lipophilicity, following a theory of hydrophobic interactions with processes of cytokinesis. It appeared possible to broaden the original database of this concept to include aneugenic as well as clastogenic compounds studied in the micronucleus (MN) test. The datasets used for this purpose were (A) the original dataset of Schultz and Onfelt [N. Schultz, A. Onfelt, Sensitivity of cytokinesis to hydrophobic interactions. Chemical induction of bi- and multi-nucleated cells, Chem. Biol. Interact. 126 (2000) 97-123.], and two sets (B, C) of our own data from studies in V79 cells in vitro. As the particular endpoints used were different (A: counts of bi- and multi-nucleated cells, B/C: micronucleus counts) the coherence of the experimental data sets was validated by including compounds belonging to both collections. Data set B included compounds with a specific effect on the mitotic spindle (nitrobenzene and benzonitrile) and data set C included the phytoestrogens genistein and daidzein, as well as a number of hormonal steroids with unknown mode of action. Taking all three data sets (A, B, C) together, the 33 compounds investigated covered a total lipophilicity range of logP between -0.51 (diamide) and 5.65 (17alpha-propylmesterolone). In order to separate statistical outliers (with a specific mode of action to be likely) from the large cluster of compounds with non-specific genotoxicity related to hydrophobic interactions, the method of robust regression was applied. It appeared that all compounds with a specific mode of action were in fact outliers of the lipophilicity rule. Genistein, a weak clastogen causing chromosomal aberrations and being discussed to induce topoisomerase-2 mediated DNA breaks, came close to the statistical borderline between compounds with specific and non-specific chromosomal genotoxicity. A general procedure is proposed, applicable in chemical product development, to screen specific and non-specific modes of action.
Insights
This study differentiates specific and non-specific genotoxicity by analyzing chemical lipophilicity and its effect on cell division. Compounds with specific mechanisms of action were identified as outliers from the general lipophilicity rule, aiding safety assessment.
Area of Science:
- Toxicology
- Genetics
- Cell Biology
Background:
- Chromosomal damage tests are crucial for genotoxicity assessment and product safety.
- Hydrophobic interactions influence cytokinesis, affecting the induction of bi- and multi-nucleated cells.
- Previous research separated non-specific agents from specific inducers based on lipophilicity.
Purpose of the Study:
- To broaden the concept of lipophilicity-based separation of genotoxic agents.
- To include aneugenic and clastogenic compounds within the micronucleus (MN) test framework.
- To develop a general procedure for screening specific and non-specific modes of action in chemical product development.
Main Methods:
- Combined three datasets (A, B, C) of genotoxicity studies in V79 cells.
- Investigated 33 compounds across a lipophilicity range (logP: -0.51 to 5.65).
- Applied robust regression to separate compounds with specific modes of action from those with non-specific, lipophilicity-related genotoxicity.
Main Results:
- All compounds with specific modes of action were identified as statistical outliers of the lipophilicity rule.
- Non-specific genotoxicity was strongly correlated with hydrophobic interactions.
- Genistein, a weak clastogen, approached the borderline between specific and non-specific genotoxicity.
Conclusions:
- Lipophilicity serves as a predictor to distinguish between specific and non-specific genotoxic mechanisms.
- The proposed method can effectively screen compounds for their mode of action in genotoxicity testing.
- This approach supports safety assessment and product development by identifying potential genotoxic risks.
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