Usage of model combination in computational toxicology.

New Approach Methodologies (NAMs) have ushered in a new era in the field of toxicology, aiming to replace animal testing. However, despite these advancements, they are not exempt from the inherent complexities associated with the study's endpoint. In this review, we have identified three major groups of complexities: mechanistic, chemical space, and methodological. The mechanistic complexity arises from interconnected biological processes within a network that are challenging to model in a single step. In the second group, chemical space complexity exhibits significant dissimilarity between compounds in the training and test series. The third group encompasses algorithmic and molecular descriptor limitations and typical class imbalance problems. To address these complexities, this work provides a guide to the usage of a combination of predictive Quantitative Structure-Activity Relationship (QSAR) models, known as metamodels. This combination of low-level models (LLMs) enables a more precise approach to the problem by focusing on different sub-mechanisms or sub-processes. For mechanistic complexity, multiple Molecular Initiating Events (MIEs) or levels of information are combined to form a mechanistic-based metamodel. Regarding the complexity arising from chemical space, two types of approaches were reviewed to construct a fragment-based chemical space metamodel: those with and without structure sharing. Metamodels with structure sharing utilize unsupervised strategies to identify data patterns and build low-level models for each cluster, which are then combined. For situations without structure sharing due to pharmaceutical industry intellectual property, the use of prediction sharing, and federated learning approaches have been reviewed. Lastly, to tackle methodological complexity, various algorithms are combined to overcome their limitations, diverse descriptors are employed to enhance problem definition and balanced dataset combinations are used to address class imbalance issues (methodological-based metamodels). Remarkably, metamodels consistently outperformed classical QSAR models across all cases, highlighting the importance of alternatives to classical QSAR models when faced with such complexities.

A continuous in silico learning strategy to identify safety liabilities in compounds used in the leather and textile industry.

There is a widely recognized need to reduce human activity's impact on the environment. Many industries of the leather and textile sector (LTI), being aware of producing a significant amount of residues (Keßler et al. 2021; Liu et al. 2021), are adopting measures to reduce the impact of their processes on the environment, starting with a more comprehensive characterization of the chemical risk associated with the substances commonly used in LTI. The present work contributes to these efforts by compiling and toxicologically annotating the substances used in LTI, supporting a continuous learning strategy for characterizing their chemical safety. This strategy combines data collection from public sources, experimental methods and in silico predictions for characterizing four different endpoints: CMR, ED, PBT, and vPvB. We present the results of a prospective validation exercise in which we confirm that in silico methods can produce reasonably good hazard estimations and fill knowledge gaps in the LTI chemical space. The proposed protocol can speed the process and optimize the use of resources including the lives of experimental animals, contributing to identifying potentially harmful substances and their possible replacement by safer alternatives, thus reducing the environmental footprint and impact on human health.

On the Integration of In Silico Drug Design Methods for Drug Repurposing.

Drug repurposing has become an important branch of drug discovery. Several computational approaches that help to uncover new repurposing opportunities and aid the discovery process have been put forward, or adapted from previous applications. A number of successful examples are now available. Overall, future developments will greatly benefit from integration of different methods, approaches and disciplines. Steps forward in this direction are expected to help to clarify, and therefore to rationally predict, new drug-target, target-disease, and ultimately drug-disease associations.