病理状态形成的连续谱在表征疾病特性方面的效用。

IF 3.5 2区 生物学 Q1 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Takashi Fujiwara, Yoshiaki Kariya, Kanata Kobayashi, Soma Matsui, Tappei Takada
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引用次数: 0

摘要

将疾病理解为从健康系统不断过渡的结果,比将其理解为离散状态更为现实。在这里,我们设计了频谱形成方法(SFA),这是一种基于机器学习的方法,可以提取有助于疾病状态连续性的关键特征。我们将SFA应用于进行性肝病和神经退行性运动障碍患者的转录组学数据,以检验其在识别生物学相关基因集方面的有效性。SFA确定了可能调节肝脏炎症和自主运动的转录因子。在神经退行性疾病中,SFA还发现了由ETS-1调控的基因,对运动的影响尚不清楚。在人类ipsc衍生神经元的功能评估中,ETS-1过表达破坏了多巴胺受体平衡,降低了gaba产生酶的水平,并促进了细胞死亡。这些发现表明,SFA能够发现能够改变疾病状态的调节因子,并为基于连续性的生物系统解释提供了一个框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Utility of the continuous spectrum formed by pathological states in characterizing disease properties.

Understanding diseases as the result of continuous transitions from a healthy system is more realistic than understanding them as discrete states. Here, we designed the spectrum formation approach (SFA), a machine learning-based method that extracts key features contributing to disease state continuity. We applied the SFA to transcriptomic data from patients with progressive liver disease and neurodegenerative movement disorders to examine its effectiveness in identifying biologically relevant gene sets. The SFA identified transcription factors that potentially regulate liver inflammation and voluntary movement. In neurodegenerative disorders, the SFA also identified genes regulated by ETS-1, with unclear effects on movement. In functional assessment using human iPSC-derived neurons, ETS-1 overexpression disrupted dopamine receptor balance, reduced GABA-producing enzyme levels, and promoted cell death. These findings suggest that the SFA enables the discovery of regulatory factors capable of modifying disease states and provides a framework for the continuity-based interpretation of biological systems.

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来源期刊
NPJ Systems Biology and Applications
NPJ Systems Biology and Applications Mathematics-Applied Mathematics
CiteScore
5.80
自引率
0.00%
发文量
46
审稿时长
8 weeks
期刊介绍: npj Systems Biology and Applications is an online Open Access journal dedicated to publishing the premier research that takes a systems-oriented approach. The journal aims to provide a forum for the presentation of articles that help define this nascent field, as well as those that apply the advances to wider fields. We encourage studies that integrate, or aid the integration of, data, analyses and insight from molecules to organisms and broader systems. Important areas of interest include not only fundamental biological systems and drug discovery, but also applications to health, medical practice and implementation, big data, biotechnology, food science, human behaviour, broader biological systems and industrial applications of systems biology. We encourage all approaches, including network biology, application of control theory to biological systems, computational modelling and analysis, comprehensive and/or high-content measurements, theoretical, analytical and computational studies of system-level properties of biological systems and computational/software/data platforms enabling such studies.
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