• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

毒理基因组学的发展:从基因表达数据理解和预测化合物诱导的毒性。

Developments in toxicogenomics: understanding and predicting compound-induced toxicity from gene expression data.

机构信息

University of Cambridge, Centre for Molecular Informatics, Department of Chemistry, Lensfield Road, Cambridge CB2 1EW, UK.

出版信息

Mol Omics. 2018 Aug 6;14(4):218-236. doi: 10.1039/c8mo00042e.

DOI:10.1039/c8mo00042e
PMID:29917034
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6080592/
Abstract

The toxicogenomics field aims to understand and predict toxicity by using 'omics' data in order to study systems-level responses to compound treatments. In recent years there has been a rapid increase in publicly available toxicological and 'omics' data, particularly gene expression data, and a corresponding development of methods for its analysis. In this review, we summarize recent progress relating to the analysis of RNA-Seq and microarray data, review relevant databases, and highlight recent applications of toxicogenomics data for understanding and predicting compound toxicity. These include the analysis of differentially expressed genes and their enrichment, signature matching, methods based on interaction networks, and the analysis of co-expression networks. In the future, these state-of-the-art methods will likely be combined with new technologies, such as whole human body models, to produce a comprehensive systems-level understanding of toxicity that reduces the necessity of in vivo toxicity assessment in animal models.

摘要

毒理基因组学领域旨在通过使用“组学”数据来理解和预测毒性,以便研究系统对化合物处理的反应。近年来,毒理学和“组学”数据(特别是基因表达数据)的公开可用性迅速增加,相应地也开发了用于分析这些数据的方法。在这篇综述中,我们总结了与 RNA-Seq 和微阵列数据分析相关的最新进展,回顾了相关数据库,并强调了毒理基因组学数据在理解和预测化合物毒性方面的最新应用。这些应用包括差异表达基因及其富集分析、特征匹配、基于相互作用网络的方法以及共表达网络分析。未来,这些最先进的方法可能会与新技术(如全人体模型)相结合,从而全面了解毒性,减少在动物模型中进行体内毒性评估的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b46/6080592/61fd4d6e5be4/c8mo00042e-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b46/6080592/b3a8e334e898/c8mo00042e-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b46/6080592/1643a22bf047/c8mo00042e-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b46/6080592/956f68db2427/c8mo00042e-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b46/6080592/f9c314571f20/c8mo00042e-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b46/6080592/d90605d83846/c8mo00042e-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b46/6080592/363c37dcfb1a/c8mo00042e-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b46/6080592/61fd4d6e5be4/c8mo00042e-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b46/6080592/b3a8e334e898/c8mo00042e-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b46/6080592/1643a22bf047/c8mo00042e-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b46/6080592/956f68db2427/c8mo00042e-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b46/6080592/f9c314571f20/c8mo00042e-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b46/6080592/d90605d83846/c8mo00042e-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b46/6080592/363c37dcfb1a/c8mo00042e-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b46/6080592/61fd4d6e5be4/c8mo00042e-f7.jpg

相似文献

1
Developments in toxicogenomics: understanding and predicting compound-induced toxicity from gene expression data.毒理基因组学的发展:从基因表达数据理解和预测化合物诱导的毒性。
Mol Omics. 2018 Aug 6;14(4):218-236. doi: 10.1039/c8mo00042e.
2
Practical application of toxicogenomics for profiling toxicant-induced biological perturbations.毒理基因组学在分析毒物诱导的生物扰动方面的实际应用。
Int J Mol Sci. 2010 Sep 20;11(9):3397-412. doi: 10.3390/ijms11093397.
3
The Japanese toxicogenomics project: application of toxicogenomics.日本毒理基因组学计划:毒理基因组学的应用。
Mol Nutr Food Res. 2010 Feb;54(2):218-27. doi: 10.1002/mnfr.200900169.
4
Use of toxicogenomics to understand mechanisms of drug-induced hepatotoxicity during drug discovery and development.在药物发现和开发过程中利用毒理基因组学来理解药物性肝损伤的机制。
Toxicol Lett. 2009 Apr 10;186(1):22-31. doi: 10.1016/j.toxlet.2008.09.017. Epub 2008 Oct 17.
5
Comparing next-generation sequencing and microarray technologies in a toxicological study of the effects of aristolochic acid on rat kidneys.比较二代测序和微阵列技术在马兜铃酸对大鼠肾脏毒性研究中的应用。
Chem Res Toxicol. 2011 Sep 19;24(9):1486-93. doi: 10.1021/tx200103b. Epub 2011 Aug 23.
6
Toxicogenomics: transcription profiling for toxicology assessment.毒理基因组学:用于毒理学评估的转录谱分析
EXS. 2009;99:325-66. doi: 10.1007/978-3-7643-8336-7_12.
7
The state-of-the-art in predictive toxicogenomics.预测毒理基因组学的最新进展。
Curr Opin Drug Discov Devel. 2006 Jan;9(1):84-91.
8
A decade of toxicogenomic research and its contribution to toxicological science.毒理基因组学研究十年及其对毒理学科学的贡献。
Toxicol Sci. 2012 Dec;130(2):217-28. doi: 10.1093/toxsci/kfs223. Epub 2012 Jul 12.
9
Widespread Dysregulation of Long Noncoding Genes Associated With Fatty Acid Metabolism, Cell Division, and Immune Response Gene Networks in Xenobiotic-exposed Rat Liver.广泛的长非编码基因失调与脂肪酸代谢、细胞分裂和免疫反应基因网络有关,发生在接触外源化学物的大鼠肝脏中。
Toxicol Sci. 2020 Apr 1;174(2):291-310. doi: 10.1093/toxsci/kfaa001.
10
Toxicogenomic module associations with pathogenesis: a network-based approach to understanding drug toxicity.毒理基因组模块与发病机制的关联:一种基于网络的理解药物毒性的方法。
Pharmacogenomics J. 2018 May 22;18(3):377-390. doi: 10.1038/tpj.2017.17. Epub 2017 Apr 25.

引用本文的文献

1
Utilizing rat kidney gene co-expression networks to enhance safety assessment biomarker identification and human translation.利用大鼠肾脏基因共表达网络增强安全性评估生物标志物的识别及向人类的转化。
iScience. 2025 Jun 21;28(7):112978. doi: 10.1016/j.isci.2025.112978. eCollection 2025 Jul 18.
2
Discovering a predictive metabolic signature of drug-induced structural cardiotoxicity in cardiac microtissues.发现心脏微组织中药物诱导的结构性心脏毒性的预测性代谢特征。
Arch Toxicol. 2025 May 16. doi: 10.1007/s00204-025-04074-4.
3
Establishment of interpretable cytotoxicity prediction models using machine learning analysis of transcriptome features.

本文引用的文献

1
A Next Generation Connectivity Map: L1000 Platform and the First 1,000,000 Profiles.下一代连接图谱:L1000平台及首批100万个图谱
Cell. 2017 Nov 30;171(6):1437-1452.e17. doi: 10.1016/j.cell.2017.10.049.
2
Comparing structural and transcriptional drug networks reveals signatures of drug activity and toxicity in transcriptional responses.比较结构药物网络和转录药物网络揭示了转录反应中药物活性和毒性的特征。
NPJ Syst Biol Appl. 2017 Aug 25;3:23. doi: 10.1038/s41540-017-0022-3. eCollection 2017.
3
CODA: Integrating multi-level context-oriented directed associations for analysis of drug effects.
利用转录组特征的机器学习分析建立可解释的细胞毒性预测模型。
Acta Pharm Sin B. 2025 Mar;15(3):1344-1358. doi: 10.1016/j.apsb.2025.02.009. Epub 2025 Feb 12.
4
Investigating the Use of Diagnostic Genes in Integrated Monitoring with a Laboratory and Field Study on Flounder ().通过对鲽鱼的实验室和实地研究,调查诊断基因在综合监测中的应用。
Toxics. 2025 Mar 12;13(3):203. doi: 10.3390/toxics13030203.
5
Bridging organ transcriptomics for advancing multiple organ toxicity assessment with a generative AI approach.利用生成式人工智能方法构建器官转录组学以推进多器官毒性评估
NPJ Digit Med. 2024 Nov 5;7(1):310. doi: 10.1038/s41746-024-01317-z.
6
Computational Strategies for Assessing Adverse Outcome Pathways: Hepatic Steatosis as a Case Study.计算策略评估不良结局途径:以肝脂肪变性为例。
Int J Mol Sci. 2024 Oct 17;25(20):11154. doi: 10.3390/ijms252011154.
7
Progress in toxicogenomics to protect human health.毒理基因组学在保护人类健康方面的进展。
Nat Rev Genet. 2025 Feb;26(2):105-122. doi: 10.1038/s41576-024-00767-1. Epub 2024 Sep 2.
8
A Network Toxicology Approach for Mechanistic Modelling of Nanomaterial Hazard and Adverse Outcomes.一种用于纳米材料危害和不良结局的机制建模的网络毒理学方法。
Adv Sci (Weinh). 2024 Aug;11(32):e2400389. doi: 10.1002/advs.202400389. Epub 2024 Jun 25.
9
Probing Liver Injuries Induced by Thioacetamide in Human In Vitro Pooled Hepatocyte Experiments.探讨硫代乙酰胺在人离体混合肝细胞实验中诱导的肝损伤。
Int J Mol Sci. 2024 Mar 13;25(6):3265. doi: 10.3390/ijms25063265.
10
Systems bioengineering approaches for developmental toxicology.发育毒理学的系统生物工程方法
Comput Struct Biotechnol J. 2023 Jun 7;21:3272-3279. doi: 10.1016/j.csbj.2023.06.005. eCollection 2023.
CODA:用于分析药物效应的多层次面向上下文的定向关联集成。
Sci Rep. 2017 Aug 8;7(1):7519. doi: 10.1038/s41598-017-07448-6.
4
Transcriptomics in toxicology.毒理学中的转录组学
Food Chem Toxicol. 2017 Nov;109(Pt 1):650-662. doi: 10.1016/j.fct.2017.07.031. Epub 2017 Jul 15.
5
A review of drug-induced liver injury databases.药物性肝损伤数据库综述。
Arch Toxicol. 2017 Sep;91(9):3039-3049. doi: 10.1007/s00204-017-2024-8. Epub 2017 Jul 17.
6
The Utility of Gene Expression Profiling from Tissue Samples to Support Drug Safety Assessments.利用组织样本中的基因表达谱来支持药物安全性评估。
ILAR J. 2017 Jul 1;58(1):69-79. doi: 10.1093/ilar/ilx016.
7
Toxicogenomic module associations with pathogenesis: a network-based approach to understanding drug toxicity.毒理基因组模块与发病机制的关联:一种基于网络的理解药物毒性的方法。
Pharmacogenomics J. 2018 May 22;18(3):377-390. doi: 10.1038/tpj.2017.17. Epub 2017 Apr 25.
8
An additional k-means clustering step improves the biological features of WGCNA gene co-expression networks.额外的k均值聚类步骤改善了WGCNA基因共表达网络的生物学特征。
BMC Syst Biol. 2017 Apr 12;11(1):47. doi: 10.1186/s12918-017-0420-6.
9
HAPPI-2: a Comprehensive and High-quality Map of Human Annotated and Predicted Protein Interactions.HAPPI-2:人类注释和预测蛋白质相互作用的全面且高质量图谱。
BMC Genomics. 2017 Feb 17;18(1):182. doi: 10.1186/s12864-017-3512-1.
10
Empirical assessment of analysis workflows for differential expression analysis of human samples using RNA-Seq.使用RNA测序对人类样本进行差异表达分析的分析流程的实证评估。
BMC Bioinformatics. 2017 Jan 17;18(1):38. doi: 10.1186/s12859-016-1457-z.