Abstract

The knowledge-based Toxtree expert system (SAR approach) was integrated with the statistically based counter propagation artificial neural network (CP ANN) model (QSAR approach) to contribute to a better mechanistic understanding of a carcinogenicity model for non-congeneric chemicals using Dragon descriptors and carcinogenic potency for rats as a response. The transparency of the CP ANN algorithm was demonstrated using intrinsic mapping technique specifically Kohonen maps. Chemical structures were represented by Dragon descriptors that express the structural and electronic features of molecules such as their shape and electronic surrounding related to reactivity of molecules. It was illustrated how the descriptors are correlated with particular structural alerts (SAs) for carcinogenicity with recognized mechanistic link to carcinogenic activity. Moreover, the Kohonen mapping technique enables one to examine the separation of carcinogens and non-carcinogens (for rats) within a family of chemicals with a particular SA for carcinogenicity. The mechanistic interpretation of models is important for the evaluation of safety of chemicals.

Highlights

  • Carcinogenicity is among the toxicological endpoints that pose limited or no prior chemical or biological classification according to the highest public concern

  • Results and Discussions contained the structural alert for carcinogenicity SA21 and with the Dragon descriptors

  • The Kohonen map enables to get clusters of congeneric particular structural alerts (SAs) for carcinogenicity In the first part of the study we described the counter propagation artificial neural network (CP artificial neural network (ANN)) model for prediction of carcinogenic class

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Summary

Introduction

Carcinogenicity is among the toxicological endpoints that pose limited or no prior chemical or biological classification according to the highest public concern. It is a challenge to represent a mechanistic interpretation for obtained results in terms of possible mechanism of carcinogenic models for prediction of carcinogenic potency for different classes of activity of studied chemicals (encoded in the carcinogenic SAs).

Results
Conclusion

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