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用于预测预防性候选药物的斑马鱼免疫靶向微阵列数据的计算研究。

Computational study of zebrafish immune-targeted microarray data for prediction of preventive drug candidates.

作者信息

Ebrahimpour Gorji Abdolvahab, Roudbari Zahra, Ebrahimpour Gorji Fatemeh, Sadeghi Balal

机构信息

Department of Fisheries, Faculty of Animal Sciences and Fisheries, Sari Agricultural and Natural Resources University, Sari, Iran.

Department of Animal Science, Faculty of Agriculture, University of Jiroft, Jiroft, Iran.

出版信息

Vet Res Forum. 2021 Winter;12(1):87-93. doi: 10.30466/vrf.2019.94179.2270. Epub 2021 Mar 15.

Abstract

Viral hemorrhagic septicemia virus (VHSV) is a rhabdovirus reported to cause economic loss in fish farms. Because of the lack of adequate preventative treatments, the identification of multipath genes involved in VHS infection might be an alternative to explore the possibility of using drugs for the seasonal prevention of this fish disease. We propose labeling a category of drug molecules by further classification and interpretation of the Drug Gene Interaction Database using gene ontology and Kyoto Encyclopedia of Genes and Genomes enrichment scores. The study investigated disease networks of up-and down-regulated genes to find those with high interaction as substantial genes in pathways among the different disease networks. We prioritized these genes based on their relationship to those associated with VHS infection in the context of human protein-protein interaction networks and disease pathways. Among the 29 genes as potential drug targets, nine were selected as promising druggable genes ( and ). PDGFRA is the most important druggable up-and down-regulated gene and is considered an important gene in the IMATINIB pathway. This study findings indicate a promising approach for drug target prediction for VHS treatment, which might be useful for disease therapeutics.

摘要

病毒性出血性败血症病毒(VHSV)是一种弹状病毒,据报道会给养鱼场造成经济损失。由于缺乏足够的预防性治疗方法,鉴定参与VHS感染的多途径基因可能是探索使用药物季节性预防这种鱼类疾病可能性的一种替代方法。我们建议通过使用基因本体论和京都基因与基因组百科全书富集分数对药物基因相互作用数据库进行进一步分类和解释,来标记一类药物分子。该研究调查了上调和下调基因的疾病网络,以找出在不同疾病网络的途径中具有高相互作用的那些基因作为关键基因。我们根据这些基因在人类蛋白质-蛋白质相互作用网络和疾病途径背景下与VHS感染相关基因的关系对它们进行了优先级排序。在作为潜在药物靶点的29个基因中,有9个被选为有前景的可成药基因(和)。血小板衍生生长因子受体α(PDGFRA)是最重要的可上调和下调的可成药基因,被认为是伊马替尼途径中的一个重要基因。这项研究结果表明了一种用于VHS治疗药物靶点预测的有前景的方法,这可能对疾病治疗有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a10/8094140/9ce52a14022e/vrf-12-87-g001.jpg

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