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本文引用的文献

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Compound cytotoxicity profiling using quantitative high-throughput screening.使用定量高通量筛选进行复合细胞毒性分析。
Environ Health Perspect. 2008 Mar;116(3):284-91. doi: 10.1289/ehp.10727.
2
Characterization of diversity in toxicity mechanism using in vitro cytotoxicity assays in quantitative high throughput screening.在定量高通量筛选中使用体外细胞毒性试验表征毒性机制的多样性
Chem Res Toxicol. 2008 Mar;21(3):659-67. doi: 10.1021/tx700365e. Epub 2008 Feb 19.
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Toxicology. Transforming environmental health protection.毒理学。转变环境卫生保护。
Science. 2008 Feb 15;319(5865):906-7. doi: 10.1126/science.1154619.
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Computer-assisted methods in chemical toxicity prediction.化学毒性预测中的计算机辅助方法。
Mini Rev Med Chem. 2007 May;7(5):499-507. doi: 10.2174/138955707780619554.
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Applying mechanisms of chemical toxicity to predict drug safety.应用化学毒性机制预测药物安全性。
Chem Res Toxicol. 2007 Mar;20(3):344-69. doi: 10.1021/tx600260a. Epub 2007 Feb 16.
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Assessing the data quality in predictive toxicology using a panel of cell lines and cytotoxicity assays.
Anal Biochem. 2007 Mar 15;362(2):221-8. doi: 10.1016/j.ab.2006.12.038. Epub 2006 Dec 28.
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Top-priority fragment QSAR approach in predicting pesticide aquatic toxicity.预测农药水生毒性的优先片段定量构效关系方法。
Chem Res Toxicol. 2006 Nov;19(11):1533-9. doi: 10.1021/tx0601814.
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Quantitative high-throughput screening: a titration-based approach that efficiently identifies biological activities in large chemical libraries.定量高通量筛选:一种基于滴定的方法,可有效识别大型化学文库中的生物活性。
Proc Natl Acad Sci U S A. 2006 Aug 1;103(31):11473-8. doi: 10.1073/pnas.0604348103. Epub 2006 Jul 24.
9
Toxicity-indicating structural patterns.毒性指示结构模式。
J Chem Inf Model. 2006 Mar-Apr;46(2):536-44. doi: 10.1021/ci050358k.
10
QSAR models for Daphnia toxicity of pesticides based on combinations of topological parameters of molecular structures.基于分子结构拓扑参数组合的农药对水蚤毒性的定量构效关系模型
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加权特征显著性:一种基于结构特征统计富集的简单、可解释的化合物毒性模型。

Weighted feature significance: a simple, interpretable model of compound toxicity based on the statistical enrichment of structural features.

机构信息

Department of Health and Human Services, NIH Chemical Genomics Center, National Institutes of Health, Bethesda, Maryland 20892-3370, USA.

出版信息

Toxicol Sci. 2009 Dec;112(2):385-93. doi: 10.1093/toxsci/kfp231. Epub 2009 Oct 4.

DOI:10.1093/toxsci/kfp231
PMID:19805409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2777082/
Abstract

In support of the U.S. Tox21 program, we have developed a simple and chemically intuitive model we call weighted feature significance (WFS) to predict the toxicological activity of compounds, based on the statistical enrichment of structural features in toxic compounds. We trained and tested the model on the following: (1) data from quantitative high-throughput screening cytotoxicity and caspase activation assays conducted at the National Institutes of Health Chemical Genomics Center, (2) data from Salmonella typhimurium reverse mutagenicity assays conducted by the U.S. National Toxicology Program, and (3) hepatotoxicity data published in the Registry of Toxic Effects of Chemical Substances. Enrichments of structural features in toxic compounds are evaluated for their statistical significance and compiled into a simple additive model of toxicity and then used to score new compounds for potential toxicity. The predictive power of the model for cytotoxicity was validated using an independent set of compounds from the U.S. Environmental Protection Agency tested also at the National Institutes of Health Chemical Genomics Center. We compared the performance of our WFS approach with classical classification methods such as Naive Bayesian clustering and support vector machines. In most test cases, WFS showed similar or slightly better predictive power, especially in the prediction of hepatotoxic compounds, where WFS appeared to have the best performance among the three methods. The new algorithm has the important advantages of simplicity, power, interpretability, and ease of implementation.

摘要

为支持美国 Tox21 计划,我们开发了一种简单且具有化学直观性的模型,我们称之为加权特征显著性(WFS),用于根据毒性化合物中结构特征的统计富集来预测化合物的毒理学活性。我们在以下方面对模型进行了训练和测试:(1)在国立卫生研究院化学基因组学中心进行的定量高通量筛选细胞毒性和半胱天冬酶激活测定的数据集,(2)由美国国家毒理学计划进行的鼠伤寒沙门氏菌回复突变性测定的数据集,以及(3)在《化学物质毒性效应登记册》中发表的肝毒性数据。毒性化合物中结构特征的富集度针对其统计学显著性进行评估,并被编译成一个简单的毒性加和模型,然后用于对新化合物进行潜在毒性评分。该模型对细胞毒性的预测能力通过使用来自美国环境保护署的独立化合物集进行验证,这些化合物也在国立卫生研究院化学基因组学中心进行了测试。我们将我们的 WFS 方法的性能与经典分类方法(如朴素贝叶斯聚类和支持向量机)进行了比较。在大多数测试案例中,WFS 显示出相似或稍好的预测能力,特别是在预测肝毒性化合物方面,WFS 似乎在这三种方法中表现最佳。新算法具有简单、强大、可解释性和易于实现的重要优势。