DRADTiP: Drug repurposing for aging disease through drug-target interaction prediction

IF 7 2区 医学 Q1 BIOLOGY Computers in biology and medicine Pub Date : 2024-09-20 DOI:10.1016/j.compbiomed.2024.109145
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Abstract

Motivation

The greatest risk factor for many non-communicable diseases is aging. Studies on model organisms have demonstrated that genetic and chemical perturbation alterations can lengthen longevity and overall health. However, finding longevity-enhancing medications and their related targets is difficult.

Method

In this work, we designed a novel drug repurposing model by identifying the interaction between aging-related genes or targets and drugs similar to aging disease. Each disease is associated with certain specific genetic factors for the occurrence of that disease. The factors include gene expression, pathway, miRNA, and degree of genes in the protein-protein interaction network. In this paper, we aim to find the drugs that prolong the life span of humans with their aging-related targets using the above-mentioned factors. In addition, the contribution or importance of each factor may vary among drugs and targets. Therefore, we designed a novel multi-layer random walk-based network representation learning model including node and edge weight to learn the features of drugs and targets respectively.

Result

The performance of the proposed model is demonstrated using k-fold cross-validation (k = 5). This model achieved better performance with scores of 0.93 and 0.91 for precision and recall respectively. The drugs identified by the system are evaluated to be potential candidates for aging since the degree of interaction between the potential drugs and their gene sets are high. In addition, the genes that are interacting with drugs produce the same biological functions. Hence the life span of the human will be increased or prolonged.

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DRADTiP:通过药物-靶点相互作用预测重新确定治疗老年疾病的药物用途
动机许多非传染性疾病的最大风险因素是衰老。对模型生物的研究表明,基因和化学扰动改变可以延长寿命和整体健康。方法在这项工作中,我们设计了一个新的药物再利用模型,通过识别衰老相关基因或靶点与类似于衰老疾病的药物之间的相互作用。每种疾病的发生都与某些特定的遗传因素有关。这些因素包括基因表达、通路、miRNA 和蛋白质-蛋白质相互作用网络中基因的程度。在本文中,我们的目标是利用上述因素,通过与衰老相关的靶点找到延长人类寿命的药物。此外,每个因素的贡献或重要性可能因药物和靶点而异。因此,我们设计了一种新颖的基于多层随机游走的网络表征学习模型,包括节点和边的权重,以分别学习药物和目标的特征。该模型的精确度和召回率分别为 0.93 和 0.91,取得了较好的性能。由于潜在药物与其基因组之间的相互作用程度较高,该系统识别出的药物被评估为潜在的衰老候选药物。此外,与药物相互作用的基因产生相同的生物功能。因此,人类的寿命将会延长。
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来源期刊
Computers in biology and medicine
Computers in biology and medicine 工程技术-工程:生物医学
CiteScore
11.70
自引率
10.40%
发文量
1086
审稿时长
74 days
期刊介绍: Computers in Biology and Medicine is an international forum for sharing groundbreaking advancements in the use of computers in bioscience and medicine. This journal serves as a medium for communicating essential research, instruction, ideas, and information regarding the rapidly evolving field of computer applications in these domains. By encouraging the exchange of knowledge, we aim to facilitate progress and innovation in the utilization of computers in biology and medicine.
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