通过网络分析探索药物不良反应和疾病表型的共同机制。

IF 4.3 Q1 BIOCHEMICAL RESEARCH METHODS
Cell Reports Methods Pub Date : 2025-02-24 Epub Date: 2025-02-14 DOI:10.1016/j.crmeth.2025.100990
Farzaneh Firoozbakht, Maria Louise Elkjaer, Diane E Handy, Rui-Sheng Wang, Zoe Chervontseva, Matthias Rarey, Joseph Loscalzo, Jan Baumbach, Olga Tsoy
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引用次数: 0

摘要

更深入地了解药物不良反应(ADR)机制对于提高药物安全性和重新利用至关重要。本研究介绍了药物不良反应机制解释器(Drug Adverse Reaction Mechanism Explainer, dream),这是一个基于网络的框架,使用全面的知识图谱来揭示不良反应和疾病表型的分子机制。通过检查药物和疾病的共同表型及其对蛋白质-蛋白质相互作用网络的影响,dream识别与ADR机制相关的蛋白质。应用于649种不良反应,DREAMER确定了67种不良反应的分子机制,包括室性心律失常和代谢性酸中毒,并强调了人格障碍和颅内出血中的gaba能信号和凝血蛋白等途径。我们进一步论证了dream在药物再利用中的应用,并提出索他洛尔、雷诺嗪和地尔硫卓作为心脏骤停的候选药物。综上所述,dream有效地检测了表型的分子机制,强调了基于网络的综合数据分析对于提高药物安全性和加速发现新的治疗策略的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring common mechanisms of adverse drug reactions and disease phenotypes through network-based analysis.

The need for a deeper understanding of adverse drug reaction (ADR) mechanisms is vital for improving drug safety and repurposing. This study introduces Drug Adverse Reaction Mechanism Explainer (DREAMER), a network-based framework that uses a comprehensive knowledge graph to uncover molecular mechanisms underlying ADRs and disease phenotypes. By examining shared phenotypes of drugs and diseases and their effects on protein-protein interaction networks, DREAMER identifies proteins linked to ADR mechanisms. Applied to 649 ADRs, DREAMER identified molecular mechanisms for 67 ADRs, including ventricular arrhythmia and metabolic acidosis, and emphasized pathways like GABAergic signaling and coagulation proteins in personality disorders and intracranial hemorrhage. We further demonstrate the application of DREAMER in drug repurposing and propose sotalol, ranolazine, and diltiazem as candidate drugs to be repurposed for cardiac arrest. In summary, DREAMER effectively detects molecular mechanisms underlying phenotypes, emphasizing the importance of network-based analyses with integrative data for enhancing drug safety and accelerating the discovery of novel therapeutic strategies.

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来源期刊
Cell Reports Methods
Cell Reports Methods Chemistry (General), Biochemistry, Genetics and Molecular Biology (General), Immunology and Microbiology (General)
CiteScore
3.80
自引率
0.00%
发文量
0
审稿时长
111 days
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