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整合组织特异性基因表达数据以改进计算机毒理基因组学方法的化学-疾病推断

Incorporating Tissue-Specific Gene Expression Data to Improve Chemical-Disease Inference of in Silico Toxicogenomics Methods.

作者信息

Wang Shan-Shan, Wang Chia-Chi, Wang Chien-Lun, Lin Ying-Chi, Tung Chun-Wei

机构信息

Ph.D. Program in Environmental and Occupational Medicine, College of Medicine, Kaohsiung Medical University and National Health Research Institutes, Kaohsiung 80708, Taiwan.

Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Miaoli County 35053, Taiwan.

出版信息

J Xenobiot. 2024 Jul 31;14(3):1023-1035. doi: 10.3390/jox14030057.

DOI:10.3390/jox14030057
PMID:39189172
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11348041/
Abstract

In silico toxicogenomics methods are resource- and time-efficient approaches for inferring chemical-protein-disease associations with potential mechanism information for exploring toxicological effects. However, current in silico toxicogenomics systems make inferences based on only chemical-protein interactions without considering tissue-specific gene/protein expressions. As a result, inferred diseases could be overpredicted with false positives. In this work, six tissue-specific expression datasets of genes and proteins were collected from the Expression Atlas. Genes were then categorized into high, medium, and low expression levels in a tissue- and dataset-specific manner. Subsequently, the tissue-specific expression datasets were incorporated into the chemical-protein-disease inference process of our ChemDIS system by filtering out relatively low-expressed genes. By incorporating tissue-specific gene/protein expression data, the enrichment rate for chemical-disease inference was largely improved with up to 62.26% improvement. A case study of melamine showed the ability of the proposed method to identify more specific disease terms that are consistent with the literature. A user-friendly user interface was implemented in the ChemDIS system. The methodology is expected to be useful for chemical-disease inference and can be implemented for other in silico toxicogenomics tools.

摘要

计算机毒理基因组学方法是一种资源和时间高效的方法,用于推断化学物质-蛋白质-疾病关联,并带有潜在机制信息以探索毒理学效应。然而,当前的计算机毒理基因组学系统仅基于化学物质-蛋白质相互作用进行推断,而未考虑组织特异性基因/蛋白质表达。因此,推断出的疾病可能会因假阳性而被过度预测。在这项工作中,从表达图谱中收集了六个基因和蛋白质的组织特异性表达数据集。然后,以组织和数据集特异性的方式将基因分为高、中、低表达水平。随后,通过滤除相对低表达的基因,将组织特异性表达数据集纳入我们的ChemDIS系统的化学物质-蛋白质-疾病推断过程。通过纳入组织特异性基因/蛋白质表达数据,化学物质-疾病推断的富集率得到了很大提高,提高幅度高达62.26%。三聚氰胺的案例研究表明,所提出的方法能够识别出与文献一致的更具体的疾病术语。在ChemDIS系统中实现了用户友好的用户界面。该方法有望用于化学物质-疾病推断,并可应用于其他计算机毒理基因组学工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336c/11348041/d8d3e91dca1b/jox-14-00057-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336c/11348041/b60a89c8c2b7/jox-14-00057-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336c/11348041/c38dd0c13a04/jox-14-00057-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336c/11348041/da4c8f819ae0/jox-14-00057-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336c/11348041/821e52dcdecd/jox-14-00057-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336c/11348041/81c691900ba0/jox-14-00057-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336c/11348041/d8d3e91dca1b/jox-14-00057-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336c/11348041/b60a89c8c2b7/jox-14-00057-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336c/11348041/c38dd0c13a04/jox-14-00057-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336c/11348041/da4c8f819ae0/jox-14-00057-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336c/11348041/821e52dcdecd/jox-14-00057-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336c/11348041/81c691900ba0/jox-14-00057-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336c/11348041/d8d3e91dca1b/jox-14-00057-g006.jpg

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本文引用的文献

1
Melamine Exacerbates Neurotoxicity in D-Galactose-Induced Neuronal SH-SY5Y Cells.三聚氰胺加剧D-半乳糖诱导的神经元SH-SY5Y细胞的神经毒性。
J Aging Res. 2023 Nov 23;2023:6635370. doi: 10.1155/2023/6635370. eCollection 2023.
2
Tissue-specific toxic effects of nano-copper on zebrafish.纳米铜对斑马鱼的组织特异性毒性作用。
Environ Res. 2024 Feb 1;242:117717. doi: 10.1016/j.envres.2023.117717. Epub 2023 Nov 21.
3
Tissue-specific transcriptome analyses in Drosophila provide novel insights into the mode of action of the insecticide spinosad and the function of its target, nAChRα6.
果蝇组织特异性转录组分析为杀虫剂多杀菌素的作用模式及其靶标 nAChRα6 的功能提供了新的见解。
Pest Manag Sci. 2023 Oct;79(10):3913-3925. doi: 10.1002/ps.7585. Epub 2023 Jun 11.
4
Advancing the Adverse Outcome Pathway for PPARγ Inactivation Leading to Pulmonary Fibrosis Using Bradford-Hill Consideration and the Comparative Toxicogenomics Database.应用布拉德福-希尔准则和比较毒理基因组学数据库推进过氧化物酶体增殖物激活受体γ失活导致肺纤维化的不良结局途径。
Chem Res Toxicol. 2022 Feb 21;35(2):233-243. doi: 10.1021/acs.chemrestox.1c00257. Epub 2022 Feb 10.
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Biological system considerations for application of toxicogenomics in next-generation risk assessment and predictive toxicology.毒理基因组学在下一代风险评估和预测毒理学中的应用的生物系统考虑因素。
Toxicol In Vitro. 2022 Apr;80:105311. doi: 10.1016/j.tiv.2022.105311. Epub 2022 Jan 14.
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A machine learning-driven approach for prioritizing food contact chemicals of carcinogenic concern based on complementary in silico methods.基于互补的计算方法,应用机器学习方法对具有致癌关注的食品接触化学物质进行优先级排序。
Food Chem Toxicol. 2022 Feb;160:112802. doi: 10.1016/j.fct.2021.112802. Epub 2022 Jan 1.
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High throughput data-based, toxicity pathway-oriented development of a quantitative adverse outcome pathway network linking AHR activation to lung damages.基于高通量数据的、以毒性通路为导向的定量不良反应途径网络的开发,将 AHR 激活与肺部损伤联系起来。
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Expression Atlas update: gene and protein expression in multiple species.ExpressionAtlas 更新:多种物种中的基因和蛋白质表达。
Nucleic Acids Res. 2022 Jan 7;50(D1):D129-D140. doi: 10.1093/nar/gkab1030.
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Nucleic Acids Res. 2021 Jan 8;49(D1):D1138-D1143. doi: 10.1093/nar/gkaa891.