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运用系统生物学方法揭示药物性肌病的潜在机制。

Uncover the Underlying Mechanism of Drug-Induced Myopathy by Using Systems Biology Approaches.

作者信息

Li Dong, Li Aixin, Zhou Hairui, Wang Xi, Li Peng, Bi Sheng, Teng Yang

机构信息

First Affiliated Hospital of Jiamusi University, Jiamusi, Heilongjiang 154002, China.

Jiamusi University, Jiamusi, Heilongjiang 154002, China.

出版信息

Int J Genomics. 2017;2017:9264034. doi: 10.1155/2017/9264034. Epub 2017 Jul 31.

Abstract

Drug-induced myopathy (DIM) is a rare side effect; however, the consequence could be fatal. There are few reports to systematically assess the underlying mechanism of DIM. In this study, we curated the comprehensive DIM drug list based on structured labeling products (SPLs) and carried out the analysis based on chemical structure space, drug protein interaction, side effect space, and transcriptomic profiling space. Some key features are enriched from each of analysis. Specifically, the similarity of DIM drugs is more significant than random chance, which shows that the chemical structure could distinguish the DIM-positive drugs from negatives. The cytochrome P450 (CYP) was identified to be shared by DIM drugs, which indicated the important role of metabolism in DIM. Three pathways including , , and enriched based on transcriptomic analysis may explain the underlying mechanism of DIM. Although the DIM is the current focus of the study, the proposed approaches could be applied to other toxicity assessments and facilitate the safety evaluation.

摘要

药物性肌病(DIM)是一种罕见的副作用;然而,其后果可能是致命的。很少有报告系统地评估DIM的潜在机制。在本研究中,我们基于结构化标签产品(SPL)策划了全面的DIM药物清单,并基于化学结构空间、药物-蛋白质相互作用、副作用空间和转录组分析空间进行了分析。从每项分析中都富集了一些关键特征。具体而言,DIM药物的相似性比随机概率更显著,这表明化学结构可以区分DIM阳性药物和阴性药物。细胞色素P450(CYP)被确定为DIM药物所共有,这表明代谢在DIM中起着重要作用。基于转录组分析富集的三条途径,包括[此处原文缺失三条途径的具体内容],可能解释了DIM的潜在机制。尽管DIM是当前的研究重点,但所提出的方法可应用于其他毒性评估,并促进安全性评价。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f9d/5554993/489251e35d9f/IJG2017-9264034.001.jpg

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