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Extending the Generalised Read-Across approach (GenRA): A systematic analysis of the impact of physicochemical property information on read-across performance

机译:扩展通用跨方法(GenRA):对理化性质信息对跨性能的影响的系统分析

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摘要

Read-across is a useful data gap filling technique used within category and analogue approaches in regulatory hazard and risk assessment. Recently we developed an algorithmic, approach called Generalised Read-Across (GenRA) () which makes read-across predictions of toxicity effects using a similarity weighted average of source analogues characterised by their chemical and/or bioactivity descriptors. A default GenRA approach (termed baseline GenRA) relies on identifying 10 source analogues relative to a target substance that are structurally similar based on Morgan chemical fingerprints and computing an activity score to estimate presence or absence of in vivo toxicity. This current study investigated the impact that similarity in bioavailability plays in altering the local neighbourhood of source analogues as well as read-across performance relative to baseline GenRA using physicochemical property information as a surrogate for bioavailability. Two approaches were evaluated: 1) a filtering approach which restricted structurally related analogues based on their physicochemical properties; and 2) a search expansion approach which included additional analogues based on a combined structural and physicochemical similarity index. Filtering minimally improved performance, and was very dependent on the similarity threshold selected. The search expansion approach performed at least as well as the baseline GenRA, and showed up to a 9% improvement in read-across performance for at least 10 of the 50 organs considered. We summarise the overall impact that physicochemical information plays on GenRA performance, illustrate the improvement for a specific case study substance and describe how to select the most appropriate physicochemical similarity threshold to achieve optimal read-across performance depending on the toxicity effect and chemical of interest. The analyses show that physicochemical property information does result in a modest (up to 9% increase) improvement in structural based read-across predictions.
机译:交叉读取是一种有用的数据空白填充技术,可用于监管风险和风险评估的类别和类似方法。最近,我们开发了一种称为通用交叉读取(GenRA)()的算法方法,该方法使用以其化学和/或生物活性描述符为特征的来源类似物的相似性加权平均值,对毒性作用进行交叉读取预测。默认的GenRA方法(称为基准GenRA)依赖于基于Morgan化学指纹识别相对于目标物质结构相似的10种来源类似物,并计算活性分数以估算体内毒性的存在或不存在。这项当前的研究使用理化性质信息作为生物利用度的替代品,研究了生物利用度的相似性在改变来源类似物的局部邻域以及相对于基准GenRA的读取跨度性能方面的影响。评价了两种方法:1)一种过滤方法,该方法基于其理化性质限制结构相关的类似物; 2)搜索扩展方法,其中包括基于组合的结构和物理化学相似性指数的其他类似物。过滤在最低程度上提高了性能,并且非常取决于所选的相似性阈值。搜索扩展方法的性能至少与基线GenRA相同,并且在所考虑的50个器官中,至少有10个器官的跨读性能提高了9%。我们总结了理化信息对GenRA性能的总体影响,说明了特定案例研究物质的改进,并描述了如何根据毒性作用和感兴趣的化学物质选择最合适的理化相似性阈值以实现最佳的交叉读取性能。分析表明,理化性质信息确实会导致基于结构的交叉预测的适度改善(最多提高9%)。

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