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癌症 DNA 甲基化分析的进展:使用非负矩阵分解和基于知识的约束来提高生物学可解释性。

Advances in cancer DNA methylation analysis with methPLIER: use of non-negative matrix factorization and knowledge-based constraints to enhance biological interpretability.

机构信息

Division of Medical AI Research and Development, National Cancer Center Research Institute, Tokyo, 104-0045, Japan.

Cancer Translational Research Team, RIKEN Center for Advanced Intelligence Project, Tokyo, 103-0027, Japan.

出版信息

Exp Mol Med. 2024 Mar;56(3):646-655. doi: 10.1038/s12276-024-01173-7. Epub 2024 Mar 4.

DOI:10.1038/s12276-024-01173-7
PMID:38433247
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10985003/
Abstract

DNA methylation is an epigenetic modification that results in dynamic changes during ontogenesis and cell differentiation. DNA methylation patterns regulate gene expression and have been widely researched. While tools for DNA methylation analysis have been developed, most of them have focused on intergroup comparative analysis within a dataset; therefore, it is difficult to conduct cross-dataset studies, such as rare disease studies or cross-institutional studies. This study describes a novel method for DNA methylation analysis, namely, methPLIER, which enables interdataset comparative analyses. methPLIER combines Pathway Level Information Extractor (PLIER), which is a non-negative matrix factorization (NMF) method, with regularization by a knowledge matrix and transfer learning. methPLIER can be used to perform intersample and interdataset comparative analysis based on latent feature matrices, which are obtained via matrix factorization of large-scale data, and factor-loading matrices, which are obtained through matrix factorization of the data to be analyzed. We used methPLIER to analyze a lung cancer dataset and confirmed that the data decomposition reflected sample characteristics for recurrence-free survival. Moreover, methPLIER can analyze data obtained via different preprocessing methods, thereby reducing distributional bias among datasets due to preprocessing. Furthermore, methPLIER can be employed for comparative analyses of methylation data obtained from different platforms, thereby reducing bias in data distribution due to platform differences. methPLIER is expected to facilitate cross-sectional DNA methylation data analysis and enhance DNA methylation data resources.

摘要

DNA 甲基化是一种表观遗传修饰,在个体发生和细胞分化过程中会发生动态变化。DNA 甲基化模式调节基因表达,已被广泛研究。虽然已经开发出用于 DNA 甲基化分析的工具,但大多数工具都集中在数据集内的组间比较分析上;因此,很难进行跨数据集的研究,如罕见病研究或跨机构研究。本研究描述了一种新的 DNA 甲基化分析方法,即 methPLIER,它能够进行跨数据集的比较分析。methPLIER 将通路水平信息提取器(PLIER)与知识矩阵正则化和迁移学习相结合,PLIER 是一种非负矩阵分解(NMF)方法。methPLIER 可以基于通过大规模数据矩阵分解获得的潜在特征矩阵以及通过要分析的数据的矩阵分解获得的因子加载矩阵,对样本和跨数据集进行比较分析。我们使用 methPLIER 分析了一个肺癌数据集,并证实数据分解反映了无复发生存的样本特征。此外,methPLIER 可以分析通过不同预处理方法获得的数据,从而减少由于预处理而导致的数据集之间的分布偏差。此外,methPLIER 可用于不同平台获得的甲基化数据的比较分析,从而减少由于平台差异导致的数据分布偏差。methPLIER 有望促进横断面 DNA 甲基化数据分析并增强 DNA 甲基化数据资源。

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Brief Bioinform. 2022 Jul 18;23(4). doi: 10.1093/bib/bbac246.
2
Genome-wide DNA methylation profiling and exome sequencing resolved a long-time misdiagnosed case.全基因组 DNA 甲基化分析和外显子组测序解决了一个长期误诊的病例。
J Hum Genet. 2022 Sep;67(9):547-551. doi: 10.1038/s10038-022-01043-y. Epub 2022 May 18.
3
Correction: Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders.
更正:临床表观基因组学:用于孟德尔疾病诊断的全基因组DNA甲基化分析。
Genet Med. 2021 Nov;23(11):2228. doi: 10.1038/s41436-021-01130-z.
4
Epigenomic analysis of 5-hydroxymethylcytosine (5hmC) reveals novel DNA methylation markers for lung cancers.组蛋白修饰分析 5-羟甲基胞嘧啶(5hmC)揭示肺癌新型 DNA 甲基化标志物。
Neoplasia. 2020 Mar;22(3):154-161. doi: 10.1016/j.neo.2020.01.001. Epub 2020 Feb 12.
5
Requirement for epithelial p38α in KRAS-driven lung tumor progression.KRAS 驱动的肺肿瘤进展中上皮细胞 p38α 的需求。
Proc Natl Acad Sci U S A. 2020 Feb 4;117(5):2588-2596. doi: 10.1073/pnas.1921404117. Epub 2020 Jan 22.
6
DNA hypermethylation associated with upregulated gene expression in prostate cancer demonstrates the diversity of epigenetic regulation.与前列腺癌中基因表达上调相关的DNA高甲基化体现了表观遗传调控的多样性。
BMC Med Genomics. 2020 Jan 8;13(1):6. doi: 10.1186/s12920-020-0657-6.
7
Epigenetics Analysis and Integrated Analysis of Multiomics Data, Including Epigenetic Data, Using Artificial Intelligence in the Era of Precision Medicine.精准医学时代的表观遗传学分析及人工智能在多组学数据(包括表观遗传学数据)的综合分析
Biomolecules. 2019 Dec 30;10(1):62. doi: 10.3390/biom10010062.
8
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9
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Nat Rev Mol Cell Biol. 2019 Oct;20(10):590-607. doi: 10.1038/s41580-019-0159-6. Epub 2019 Aug 9.
10
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