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. 2022:2425:149-183.
doi: 10.1007/978-1-0716-1960-5_7.

In Silico Prediction of Chemically Induced Mutagenicity: A Weight of Evidence Approach Integrating Information from QSAR Models and Read-Across Predictions

Affiliations

In Silico Prediction of Chemically Induced Mutagenicity: A Weight of Evidence Approach Integrating Information from QSAR Models and Read-Across Predictions

Enrico Mombelli et al. Methods Mol Biol. 2022.

Abstract

Information on genotoxicity is an essential piece of information in the framework of several regulations aimed at evaluating chemical toxicity. In this context, QSAR models that can predict Ames genotoxicity can conveniently provide relevant information. Indeed, they can be straightforwardly and rapidly used for predicting the presence or absence of genotoxic hazards associated with the interactions of chemicals with DNA. Nevertheless, and despite their ease of use, the main interpretative challenge is related to a critical assessment of the information that can be gathered, thanks to these tools. This chapter provides guidance on how to use freely available QSAR and read-across tools provided by VEGA HUB and on how to interpret their predictions according to a weight-of-evidence approach.

Keywords: Ames test; Mutagenicity; Predictive reliability; QSAR; Structural alerts.

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References

    1. Moore MM, Myers MB, Heflich RH (2000) Mutagenesis and genetic toxicology. In: Williams PL, James RC, Roberts SM (eds) Principles of toxicology: environmental and industrial applications. Wiley-Interscience, New York, pp 239–264
    1. Sutter A, Amberg A, Boyer S, Brigo A, Contrera JF, Custer LL, Dobo KL, Gervais V, Glowienke S, van Gompel J, Greene N, Muster W, Nicolette J, Reddy MV, Thybaud V, Vock E, White AT, Müller L (2013) Use of in silico systems and expert knowledge for structure-based assessment of potentially mutagenic impurities. Regul Toxicol Pharmacol 67(1):39–52. https://doi.org/10.1016/j.yrtph.2013.05.001 - DOI - PubMed
    1. EC (2006) Regulation (EC) No 1907/2006 of the European Parliament and of the Council of 18 December 2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), establishing a European Chemicals Agency, amending Directive 1999/45/EC and repealing Council Regulation (EEC) No 793/93 and Commission Regulation (EC) No 1488/94 as well as Council Directive 76/769/EEC and Commission Directives 91/155/EEC, 93/67/EEC, 93/105/EC and 2000/21/EC, The European Parliament and the Council of the European Union
    1. Ames BN, McCann J, Yamasaki E (1975) Methods for detecting carcinogens and mutagens with the salmonella/mammalian-microsome mutagenicity test. Mutat Res 31(6):347–364 - DOI
    1. Claxton LD, Umbuzeiro Gde A, DeMarini DM (2010) The salmonella mutagenicity assay: the stethoscope of genetic toxicology for the 21st century. Environ Health Perspect 118(11):1515–1522 - DOI

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