• 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

代谢组学驱动的药物发现中治疗靶点识别方法。

Metabolomics-driven approaches for identifying therapeutic targets in drug discovery.

作者信息

Pan Shanshan, Yin Luan, Liu Jie, Tong Jie, Wang Zichuan, Zhao Jiahui, Liu Xuesong, Chen Yong, Miao Jing, Zhou Yuan, Zeng Su, Xu Tengfei

机构信息

Research Center for Clinical Pharmacy College of Pharmaceutical Sciences Zhejiang University Hangzhou Zhejiang China.

College of Pharmaceutical Sciences Zhejiang University Hangzhou Zhejiang China.

出版信息

MedComm (2020). 2024 Nov 11;5(11):e792. doi: 10.1002/mco2.792. eCollection 2024 Nov.

DOI:10.1002/mco2.792
PMID:39534557
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11555024/
Abstract

Identification of therapeutic targets can directly elucidate the mechanism and effect of drug therapy, which is a central step in drug development. The disconnect between protein targets and phenotypes under complex mechanisms hampers comprehensive target understanding. Metabolomics, as a systems biology tool that captures phenotypic changes induced by exogenous compounds, has emerged as a valuable approach for target identification. A comprehensive overview was provided in this review to illustrate the principles and advantages of metabolomics, delving into the application of metabolomics in target identification. This review outlines various metabolomics-based methods, such as dose-response metabolomics, stable isotope-resolved metabolomics, and multiomics, which identify key enzymes and metabolic pathways affected by exogenous substances through dose-dependent metabolite-drug interactions. Emerging techniques, including single-cell metabolomics, artificial intelligence, and mass spectrometry imaging, are also explored for their potential to enhance target discovery. The review emphasizes metabolomics' critical role in advancing our understanding of disease mechanisms and accelerating targeted drug development, while acknowledging current challenges in the field.

摘要

治疗靶点的识别能够直接阐明药物治疗的机制和效果,这是药物研发中的核心步骤。在复杂机制下,蛋白质靶点与表型之间的脱节阻碍了对靶点的全面理解。代谢组学作为一种能够捕捉外源性化合物诱导的表型变化的系统生物学工具,已成为一种有价值的靶点识别方法。本综述提供了一个全面的概述,以阐述代谢组学的原理和优势,并深入探讨代谢组学在靶点识别中的应用。本综述概述了各种基于代谢组学的方法,如剂量反应代谢组学、稳定同位素分辨代谢组学和多组学,这些方法通过剂量依赖性代谢物 - 药物相互作用来识别受外源性物质影响的关键酶和代谢途径。还探讨了新兴技术,包括单细胞代谢组学、人工智能和质谱成像在增强靶点发现方面的潜力。该综述强调了代谢组学在推进我们对疾病机制的理解和加速靶向药物研发方面的关键作用,同时也承认了该领域当前面临的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/11555024/7e669ccd581b/MCO2-5-e792-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/11555024/a93488f2dc9b/MCO2-5-e792-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/11555024/0f3fe4bb0364/MCO2-5-e792-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/11555024/adb43a3b9675/MCO2-5-e792-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/11555024/9ea5daf02cc5/MCO2-5-e792-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/11555024/78112dfbda8a/MCO2-5-e792-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/11555024/b71bb7cde02d/MCO2-5-e792-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/11555024/1c9f561ddfb7/MCO2-5-e792-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/11555024/ffb7ac473a87/MCO2-5-e792-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/11555024/7e669ccd581b/MCO2-5-e792-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/11555024/a93488f2dc9b/MCO2-5-e792-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/11555024/0f3fe4bb0364/MCO2-5-e792-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/11555024/adb43a3b9675/MCO2-5-e792-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/11555024/9ea5daf02cc5/MCO2-5-e792-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/11555024/78112dfbda8a/MCO2-5-e792-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/11555024/b71bb7cde02d/MCO2-5-e792-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/11555024/1c9f561ddfb7/MCO2-5-e792-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/11555024/ffb7ac473a87/MCO2-5-e792-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/11555024/7e669ccd581b/MCO2-5-e792-g005.jpg

相似文献

1
Metabolomics-driven approaches for identifying therapeutic targets in drug discovery.代谢组学驱动的药物发现中治疗靶点识别方法。
MedComm (2020). 2024 Nov 11;5(11):e792. doi: 10.1002/mco2.792. eCollection 2024 Nov.
2
Translational Metabolomics of Head Injury: Exploring Dysfunctional Cerebral Metabolism with Ex Vivo NMR Spectroscopy-Based Metabolite Quantification头部损伤的转化代谢组学:基于体外核磁共振波谱的代谢物定量分析探索脑代谢功能障碍
3
Metabolomics for Clinical Biomarker Discovery and Therapeutic Target Identification.代谢组学在临床生物标志物发现和治疗靶点鉴定中的应用。
Molecules. 2024 May 8;29(10):2198. doi: 10.3390/molecules29102198.
4
[Application of multiomics mass spectrometry in the research of chemical exposome].多组学质谱技术在化学暴露组学研究中的应用
Se Pu. 2024 Feb;42(2):120-130. doi: 10.3724/SP.J.1123.2023.10001.
5
Advances in Mass Spectrometry-Based Blood Metabolomics Profiling for Non-Cancer Diseases: A Comprehensive Review.基于质谱的非癌症疾病血液代谢组学分析进展:综述
Metabolites. 2024 Jan 14;14(1):54. doi: 10.3390/metabo14010054.
6
Metabolomics and lipidomics strategies in modern drug discovery and development.代谢组学和脂质组学策略在现代药物发现和开发中的应用。
Drug Discov Today. 2023 Oct;28(10):103751. doi: 10.1016/j.drudis.2023.103751. Epub 2023 Aug 26.
7
Stable isotope-resolved metabolomics and applications for drug development.稳定同位素分辨代谢组学及其在药物开发中的应用。
Pharmacol Ther. 2012 Mar;133(3):366-91. doi: 10.1016/j.pharmthera.2011.12.007. Epub 2011 Dec 23.
8
Functional metabolomics innovates therapeutic discovery of traditional Chinese medicine derived functional compounds.功能代谢组学创新了中药来源功能化合物的治疗发现。
Pharmacol Ther. 2021 Aug;224:107824. doi: 10.1016/j.pharmthera.2021.107824. Epub 2021 Mar 2.
9
Spatially resolved metabolomics: From metabolite mapping to function visualising.空间分辨代谢组学:从代谢物映射到功能可视化。
Clin Transl Med. 2024 Nov;14(11):e70031. doi: 10.1002/ctm2.70031.
10
Metabolomics- and systems-biology-guided discovery of metabolite lead compounds and druggable targets.代谢组学和系统生物学指导的代谢物先导化合物和可药物靶点的发现。
Drug Discov Today. 2023 Feb;28(2):103460. doi: 10.1016/j.drudis.2022.103460. Epub 2022 Nov 24.

引用本文的文献

1
Genetic Architecture of Ischemic Stroke: Insights from Genome-Wide Association Studies and Beyond.缺血性中风的遗传结构:全基因组关联研究及其他方面的见解
J Cardiovasc Dev Dis. 2025 Jul 23;12(8):281. doi: 10.3390/jcdd12080281.
2
Synergistic integration of extracellular vesicles and metal-organic frameworks: unlocking new opportunities in disease diagnosis and therapy.细胞外囊泡与金属有机框架的协同整合:为疾病诊断和治疗开启新机遇
Theranostics. 2025 Jul 28;15(16):8609-8638. doi: 10.7150/thno.113474. eCollection 2025.
3
A comprehensive review on computational metabolomics: Advancing multiscale analysis through approaches.

本文引用的文献

1
Multitarget antibacterial drugs: An effective strategy to combat bacterial resistance.多靶点抗菌药物:对抗细菌耐药性的有效策略。
Pharmacol Ther. 2023 Oct 28:108550. doi: 10.1016/j.pharmthera.2023.108550.
2
Single Cell mass spectrometry: Towards quantification of small molecules in individual cells.单细胞质谱分析:迈向单个细胞中小分子的定量分析。
Trends Analyt Chem. 2024 May;174. doi: 10.1016/j.trac.2024.117657. Epub 2024 Mar 19.
3
Revisiting liver metabolism through acetyl-CoA carboxylase inhibition.重新审视通过乙酰辅酶 A 羧化酶抑制作用对肝脏代谢的影响。
关于计算代谢组学的全面综述:通过多种方法推进多尺度分析。
Comput Struct Biotechnol J. 2025 Jul 13;27:3191-3215. doi: 10.1016/j.csbj.2025.07.016. eCollection 2025.
4
The Utility of Metabolomics in Spinal Cord Injury: Opportunities for Biomarker Discovery and Neuroprotection.代谢组学在脊髓损伤中的应用:生物标志物发现与神经保护的机遇
Int J Mol Sci. 2025 Jul 17;26(14):6864. doi: 10.3390/ijms26146864.
5
Current Bioinformatics Tools in Precision Oncology.精准肿瘤学中的当前生物信息学工具
MedComm (2020). 2025 Jul 9;6(7):e70243. doi: 10.1002/mco2.70243. eCollection 2025 Jul.
6
Stepping out of the dark: how metabolomics shed light on fungal biology.走出黑暗:代谢组学如何揭示真菌生物学奥秘
FEMS Microbiol Rev. 2025 Jan 14;49. doi: 10.1093/femsre/fuaf028.
7
From Biomarker Discovery to Clinical Applications of Metabolomics in Glioblastoma.从生物标志物发现到代谢组学在胶质母细胞瘤中的临床应用
Metabolites. 2025 Apr 29;15(5):295. doi: 10.3390/metabo15050295.
8
Discovery of biological markers for schizophrenia based on metabolomics: a systematic review.基于代谢组学的精神分裂症生物标志物发现:一项系统综述
Front Psychiatry. 2025 Mar 28;16:1540260. doi: 10.3389/fpsyt.2025.1540260. eCollection 2025.
Trends Endocrinol Metab. 2024 Jul;35(7):563-565. doi: 10.1016/j.tem.2024.04.010. Epub 2024 Apr 24.
4
HIF1α-dependent uncoupling of glycolysis suppresses tumor cell proliferation.缺氧诱导因子 1α(HIF1α)依赖性糖酵解解偶联抑制肿瘤细胞增殖。
Cell Rep. 2024 Apr 23;43(4):114103. doi: 10.1016/j.celrep.2024.114103. Epub 2024 Apr 11.
5
Meta-metabolomic responses of river biofilms to cobalt exposure and use of dose-response model trends as an indicator of effects.河川生物膜对钴暴露的元代谢组学响应,以及利用剂量-反应模型趋势作为效应指示物。
J Hazard Mater. 2024 May 15;470:134099. doi: 10.1016/j.jhazmat.2024.134099. Epub 2024 Mar 20.
6
One-Shot Single-Cell Proteome and Metabolome Analysis Strategy for the Same Single Cell.一种对单个细胞进行同时的单细胞蛋白质组和代谢组分析的策略。
Anal Chem. 2024 Apr 9;96(14):5499-5508. doi: 10.1021/acs.analchem.3c05659. Epub 2024 Mar 28.
7
STEP: profiling cellular-specific targets and pathways of bioactive small molecules in tissues integrating single-cell transcriptomics and chemoproteomics.步骤:整合单细胞转录组学和化学蛋白质组学,分析生物活性小分子在组织中的细胞特异性靶点和信号通路。
Chem Sci. 2024 Mar 5;15(12):4313-4321. doi: 10.1039/d3sc04826h. eCollection 2024 Mar 20.
8
A small-molecule TNIK inhibitor targets fibrosis in preclinical and clinical models.一种小分子TNIK抑制剂在临床前和临床模型中靶向纤维化。
Nat Biotechnol. 2025 Jan;43(1):63-75. doi: 10.1038/s41587-024-02143-0. Epub 2024 Mar 8.
9
Stable Isotope Tracer Technique and Network Pharmacology to Reveal Antidepressant Targets and Active Components of Xiaoyao San.稳定同位素示踪技术结合网络药理学揭示逍遥散抗抑郁作用的靶点及活性成分。
Chem Biodivers. 2024 Apr;21(4):e202301736. doi: 10.1002/cbdv.202301736. Epub 2024 Mar 27.
10
Hepatic malonyl-CoA synthesis restrains gluconeogenesis by suppressing fat oxidation, pyruvate carboxylation, and amino acid availability.肝酰基辅酶 A 的合成通过抑制脂肪氧化、丙酮酸羧化和氨基酸可用性来抑制糖异生。
Cell Metab. 2024 May 7;36(5):1088-1104.e12. doi: 10.1016/j.cmet.2024.02.004. Epub 2024 Mar 5.