构建基于通路的加权网络分析2型糖尿病相关基因。

IF 1.9 4区 生物学 Q4 CELL BIOLOGY
Xue-Yan Zhang, Chuan-Yun Xu, Ke-Fei Cao, Hong Luo, Xu-Sheng Zhang
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引用次数: 0

摘要

复杂网络是研究复杂疾病的有效途径,通过阐明疾病各因素之间的相互作用,为理解复杂疾病的病理机制提供了另一个视角。2型糖尿病(T2DM)是一种涉及遗传和环境因素的复杂多基因代谢性疾病。本研究将复杂网络方法与生物学数据相结合,构建了t2dm相关基因的基于路径的加权网络模型,以探索基因之间的相互关系,根据与边缘相连的两个节点(基因)所涉及的相同路径的数量为每个边缘分配权重。边权值可以反映节点(基因)之间的连接(相互作用)强度的差异,直观地反映了基因之间的生物相关程度,并有助于节点的重要性。统计特征和拓扑特征分析表明,边权值与网络拓扑结构相关,且边权值呈幂律衰减。权值的差异表明,同一度节点的边权分布权值近似相等;而且大多数权值较高的边都倾向于与度较高的节点连接。为了确定加权网络的关键枢纽基因,采用综合排序指标综合反映节点的强度、程度和路径数三个指标的贡献;采用综合排序指数大于0.56的阈值,鉴定出12个关键枢纽基因:MAPK1、PIK3CD、PIK3CA、PIK3R1、AKT2、AKT1、KRAS、TNF、MAPK8、PRKCA、IL6和MTOR。这些基因在T2DM的发生和发展中应发挥重要作用,可作为潜在的治疗靶点,进一步开展其在T2DM中的生物学和医学功能研究。可以预期,将复杂网络方法与其他数据分析技术相结合,可以为未来探索T2DM等复杂疾病的发病机制和治疗提供更多线索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of type 2 diabetes mellitus-related genes by constructing the pathway-based weighted network.

Complex network is an effective approach to studying complex diseases, and provides another perspective for understanding their pathological mechanisms by illustrating the interactions between various factors of diseases. Type 2 diabetes mellitus (T2DM) is a complex polygenic metabolic disease involving genetic and environmental factors. By combining the complex network approach with biological data, this study constructs a pathway-based weighted network model of T2DM-related genes to explore the interrelationships between genes, here a weight is assigned to each edge in terms of the number of the same pathways in which the two nodes (genes) connected to the edge are involved. The edge weights can reflect differences in the strength of connections (interactions) between nodes (genes), which intuitively reflect the extent of biological correlations between genes and contribute to the importance of the nodes. Analysis of statistical and topological characteristics shows that the edge weights are correlated to the network topology, and the edge weight distribution decays as a power-law. The disparity of the weights indicates that the edge weight distribution for the nodes with the same degree is of approximately equal weights; and most edges with the higher weights tend to connect with the higher degree nodes. To determine the key hub genes of the weighted network, an integrated ranking index is used to comprehensively reflect the contribution of the three indices (strength, degree and number of pathways) of nodes; by taking the threshold of integrated ranking index greater than 0.56, 12 key hub genes are identified: MAPK1, PIK3CD, PIK3CA, PIK3R1, AKT2, AKT1, KRAS, TNF, MAPK8, PRKCA, IL6 and MTOR. These genes should play an important role in the occurrence and development of T2DM, and can be regarded as potential therapeutic targets for further biological and medical research on their functions in T2DM. It can be expected that combining complex network approach with other data analysis techniques can provide more clues for exploring the pathogenesis and treatment of T2DM and other complex diseases in the future.

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来源期刊
IET Systems Biology
IET Systems Biology 生物-数学与计算生物学
CiteScore
4.20
自引率
4.30%
发文量
17
审稿时长
>12 weeks
期刊介绍: IET Systems Biology covers intra- and inter-cellular dynamics, using systems- and signal-oriented approaches. Papers that analyse genomic data in order to identify variables and basic relationships between them are considered if the results provide a basis for mathematical modelling and simulation of cellular dynamics. Manuscripts on molecular and cell biological studies are encouraged if the aim is a systems approach to dynamic interactions within and between cells. The scope includes the following topics: Genomics, transcriptomics, proteomics, metabolomics, cells, tissue and the physiome; molecular and cellular interaction, gene, cell and protein function; networks and pathways; metabolism and cell signalling; dynamics, regulation and control; systems, signals, and information; experimental data analysis; mathematical modelling, simulation and theoretical analysis; biological modelling, simulation, prediction and control; methodologies, databases, tools and algorithms for modelling and simulation; modelling, analysis and control of biological networks; synthetic biology and bioengineering based on systems biology.
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