Multi-omics data integration for subtype identification of Chinese lower-grade gliomas: A joint similarity network fusion approach

被引:3
|
作者
Li, Lingmei [1 ]
Wei, Yifang [1 ]
Shi, Guojing [1 ]
Yang, Haitao [2 ]
Li, Zhi [3 ]
Fang, Ruiling [1 ]
Cao, Hongyan [1 ,4 ,6 ]
Cui, Yuehua [5 ,6 ]
机构
[1] Shanxi Med Univ, Sch Publ Hlth, Div Hlth Stat, Taiyuan 030001, Shanxi, Peoples R China
[2] Hebei Med Univ, Sch Publ Hlth, Div Hlth Stat, Shijiazhuang 050017, Hebei, Peoples R China
[3] Shanxi Med Univ, Taiyuan Cent Hosp, Dept Hematol, Taiyuan 030001, Shanxi, Peoples R China
[4] Shanxi Med Univ, Yidu Cloud Inst Med Data Sci, Taiyuan 030001, Shanxi, Peoples R China
[5] Michigan State Univ, Dept Stat & Probabil, E Lansing, MI 48824 USA
[6] Shanxi Med Univ, Sch Publ Hlth, Div Hlth Stat, Taiyuan, Shanxi, Peoples R China
关键词
Joint-SNF; LGG; Multi-omics data integration; Subtypes identification; MUTATIONS; CDC45;
D O I
10.1016/j.csbj.2022.06.065
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lower-grade gliomas (LGG), characterized by heterogeneity and invasiveness, originate from the central nervous system. Although studies focusing on molecular subtyping and molecular characteristics have provided novel insights into improving the diagnosis and therapy of LGG, there is an urgent need to identify new molecular subtypes and biomarkers that are promising to improve patient survival outcomes. Here, we proposed a joint similarity network fusion (Joint-SNF) method to integrate different omics data types to construct a fused network using the Joint and Individual Variation Explained (JIVE) technique under the SNF framework. Focusing on the joint network structure, a spectral clustering method was employed to obtain subtypes of patients. Simulation studies show that the proposed Joint-SNF method outperforms the original SNF approach under various simulation scenarios. We further applied the method to a Chinese LGG data set including mRNA expression, DNA methylation and microRNA (miRNA). Three molecular subtypes were identified and showed statistically significant differences in patient survival outcomes. The five-year mortality rates of the three subtypes are 80.8%, 32.1%, and 34.4%, respectively. After adjusting for clinically relevant covariates, the death risk of patients in Cluster 1 was 5.06 times higher than patients in other clusters. The fused network attained by the proposed Joint-SNF method enhances strong similarities, thus greatly improves subtyping performance compared to the original SNF method. The findings in the real application may provide important clues for improving patient survival outcomes and for precision treatment for Chinese LGG patients. An R package to implement the method can be accessed in Github at https://github.com/Sameerer/Joint-SNF.(c) 2022 The Author(s). Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:3482 / 3492
页数:11
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