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解析分子谜题:探索不同 EMT 状态细胞系中的基因网络。

Unraveling the Molecular Puzzle: Exploring Gene Networks across Diverse EMT Status of Cell Lines.

机构信息

School of Mathematics, Statistics and Data Science, Sungshin Women's University, Seoul 02844, Republic of Korea.

出版信息

Int J Mol Sci. 2023 Aug 14;24(16):12784. doi: 10.3390/ijms241612784.

DOI:10.3390/ijms241612784
PMID:37628965
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10454379/
Abstract

Understanding complex disease mechanisms requires a comprehensive understanding of the gene regulatory networks, as complex diseases are often characterized by the dysregulation and dysfunction of molecular networks, rather than abnormalities in single genes. Specifically, the exploration of cell line-specific gene networks can provide essential clues for precision medicine, as this methodology can uncover molecular interplays specific to particular cell line statuses, such as drug sensitivity, cancer progression, etc. In this article, we provide a comprehensive review of computational strategies for cell line-specific gene network analysis: (1) cell line-specific gene regulatory network estimation and analysis of gene networks under varying epithelial-mesenchymal transition (EMT) statuses of cell lines; and (2) an explainable artificial intelligence approach for interpreting the estimated massive multiple EMT-status-specific gene networks. The objective of this review is to help readers grasp the concept of computational network biology, which holds significant implications for precision medicine by offering crucial clues.

摘要

理解复杂疾病机制需要全面了解基因调控网络,因为复杂疾病通常表现为分子网络的失调和功能障碍,而不是单个基因的异常。具体来说,探索细胞系特异性基因网络可以为精准医学提供重要线索,因为这种方法可以揭示特定于特定细胞系状态的分子相互作用,例如药物敏感性、癌症进展等。在本文中,我们提供了细胞系特异性基因网络分析的计算策略的全面综述:(1)细胞系特异性基因调控网络估计和分析细胞系中不同上皮-间充质转化(EMT)状态下的基因网络;(2)用于解释估计的大量 EMT 状态特异性基因网络的可解释人工智能方法。本综述的目的是帮助读者掌握计算网络生物学的概念,这通过提供关键线索对精准医学具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e9b/10454379/3d0a9226bdc0/ijms-24-12784-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e9b/10454379/351cf7622bf1/ijms-24-12784-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e9b/10454379/3d0a9226bdc0/ijms-24-12784-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e9b/10454379/351cf7622bf1/ijms-24-12784-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e9b/10454379/3d0a9226bdc0/ijms-24-12784-g002.jpg

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本文引用的文献

1
Gene regulatory network inference in the era of single-cell multi-omics.单细胞多组学时代的基因调控网络推断
Nat Rev Genet. 2023 Nov;24(11):739-754. doi: 10.1038/s41576-023-00618-5. Epub 2023 Jun 26.
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A comprehensive overview and critical evaluation of gene regulatory network inference technologies.基因调控网络推断技术的全面概述和批判性评估。
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Global gene network exploration based on explainable artificial intelligence approach.基于可解释人工智能方法的全球基因网络探索。
PLoS One. 2020 Nov 6;15(11):e0241508. doi: 10.1371/journal.pone.0241508. eCollection 2020.
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Unresolved Complexity in the Gene Regulatory Network Underlying EMT.上皮-间质转化(EMT)相关基因调控网络中尚未解决的复杂性
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IFI16, a nuclear innate immune DNA sensor, mediates epigenetic silencing of herpesvirus genomes by its association with H3K9 methyltransferases SUV39H1 and GLP.IFI16,一种核先天免疫 DNA 传感器,通过与 H3K9 甲基转移酶 SUV39H1 和 GLP 的结合,介导疱疹病毒基因组的表观遗传沉默。
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p38-regulated FOXC1 stability is required for colorectal cancer metastasis.p38 调控的 FOXC1 稳定性是结直肠癌转移所必需的。
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IRF6 Is Directly Regulated by ZEB1 and ELF3, and Predicts a Favorable Prognosis in Gastric Cancer.IRF6受ZEB1和ELF3直接调控,并预测胃癌的预后良好。
Front Oncol. 2019 Apr 4;9:220. doi: 10.3389/fonc.2019.00220. eCollection 2019.
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