Predicting latent lncRNA and cancer metastatic event associations via variational graph auto-encoder

被引:3
|
作者
Zhu, Yuan [1 ,2 ,3 ]
Zhang, Feng [4 ]
Zhang, Shihua [5 ]
Yi, Ming [4 ]
机构
[1] China Univ Geosci, Sch Automat, 388 Lumo Rd, Wuhan 430074, Hubei, Peoples R China
[2] Hubei Key Lab Adv Control & Intelligent Automat Co, 388 Lumo Rd, Wuhan 430074, Hubei, Peoples R China
[3] Engn Res Ctr Intelligent Technol Geoexplorat, 388 Lumo Rd, Wuhan 430074, Hubei, Peoples R China
[4] China Univ Geosci, Sch Math & Phys, 388 Lumo Rd, Wuhan 430074, Hubei, Peoples R China
[5] Wuhan Univ Sci & Technol, Coll Life Sci & Hlth, 974 Heping Ave, Wuhan 430081, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
lncRNA; Cancer metastatic events; Variational graph auto-encoder; Interaction prediction; NONCODING RNA; BREAST-CANCER; CELL-MIGRATION; CARCINOMA-CELL; MT1JP; CONTRIBUTES; SUPPRESSES; PROLIFERATION; INVASION; MEG3;
D O I
10.1016/j.ymeth.2023.01.006
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Long non-coding RNA (lncRNA) are shown to be closely associated with cancer metastatic events (CME, e.g., cancer cell invasion, intravasation, extravasation, proliferation) that collaboratively accelerate malignant cancer spread and cause high mortality rate in patients. Clinical trials may accurately uncover the relationships between lncRNAs and CMEs; however, it is time-consuming and expensive. With the accumulation of data, there is an urgent need to find efficient ways to identify these relationships. Herein, a graph embedding representation-based predictor (VGEA-LCME) for exploring latent lncRNA-CME associations is introduced. In VGEA-LCME, a heterogeneous combined network is constructed by integrating similarity and linkage matrix that can maintain internal and external characteristics of networks, and a variational graph auto-encoder serves as a feature generator to represent arbitrary lncRNA and CME pair. The final robustness predicted result is obtained by ensemble classifier strategy via cross-validation. Experimental comparisons and literature verification show better remarkable performance of VGEA-LCME, although the similarities between CMEs are challenging to calculate. In addition, VGEA-LCME can further identify organ-specific CMEs. To the best of our knowledge, this is the first computational attempt to discover the potential relationships between lncRNAs and CMEs. It may provide support and new insight for guiding experimental research of metastatic cancers. The source code and data are available at https://github .com /zhuyuan -cug /VGAE-LCME.
引用
收藏
页码:1 / 9
页数:9
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