TY - JOUR
T1 - MuGNet-CMI
T2 - Multi-Head Hybrid Graph Neural Network for Predicting circRNA-miRNA Interactions With Global High-Order and Local Low-Order Information
AU - Jiang, Chen
AU - Wang, Lei
AU - Yu, Changqing
AU - You, Zhuhong
AU - Wang, Xinfei
AU - Wei, Mengmeng
AU - Lu, Mianshuo
N1 - Publisher Copyright:
© 2015 IEEE.
PY - 2026/2
Y1 - 2026/2
N2 - Circular RNAs (circRNAs) are non-coding RNA molecules that play a crucial role in regulating genes and contributing to disease progression. CircRNAs can function as sponges for microRNAs (miRNAs), thereby regulating gene expression and influencing disease outcomes. Identifying associations between circRNAs and miRNAs through computational methods enhances the understanding of complex disease mechanisms and offers a reliable tool for pre-selecting candidates for experimental validation. Existing models, however, are limited in their ability to capture either global or local node information, the prediction of circRNA and miRNA interactions is still challenging. In order to effectively deal with this problem, we propose a novel framework for predicting circRNA-miRNA interactions (CMIs), known as MuGNet-CMI, which leverages multi-head hybrid graph neural network and global high-order and local low-order information. The model employs the MetaPath2Vec algorithm to generate high-quality node embeddings within the circRNA-miRNA heterogeneous matrix. The multi-head dynamic attention mechanism, combined with GraphSAGE, is incorporated to efficiently capture both global high-order and local low-order node information. Additionally, we integrate neural aggregators into the multi-head dynamic attention mechanism to aggregate feature information from the captured nodes. Validation using three real datasets demonstrates that MuGNet-CMI delivers good performance in predicting CMIs, offering valuable insights to guide experimental research in gene regulation.
AB - Circular RNAs (circRNAs) are non-coding RNA molecules that play a crucial role in regulating genes and contributing to disease progression. CircRNAs can function as sponges for microRNAs (miRNAs), thereby regulating gene expression and influencing disease outcomes. Identifying associations between circRNAs and miRNAs through computational methods enhances the understanding of complex disease mechanisms and offers a reliable tool for pre-selecting candidates for experimental validation. Existing models, however, are limited in their ability to capture either global or local node information, the prediction of circRNA and miRNA interactions is still challenging. In order to effectively deal with this problem, we propose a novel framework for predicting circRNA-miRNA interactions (CMIs), known as MuGNet-CMI, which leverages multi-head hybrid graph neural network and global high-order and local low-order information. The model employs the MetaPath2Vec algorithm to generate high-quality node embeddings within the circRNA-miRNA heterogeneous matrix. The multi-head dynamic attention mechanism, combined with GraphSAGE, is incorporated to efficiently capture both global high-order and local low-order node information. Additionally, we integrate neural aggregators into the multi-head dynamic attention mechanism to aggregate feature information from the captured nodes. Validation using three real datasets demonstrates that MuGNet-CMI delivers good performance in predicting CMIs, offering valuable insights to guide experimental research in gene regulation.
KW - CircRNAs
KW - GraphSAGE
KW - MetaPath2Vec
KW - circRNA-miRNA interactions
KW - miRNAs
KW - multi-head dynamic attention mechanism
UR - https://www.scopus.com/pages/publications/105014604874
U2 - 10.1109/TBDATA.2025.3604175
DO - 10.1109/TBDATA.2025.3604175
M3 - 文章
AN - SCOPUS:105014604874
SN - 2332-7790
VL - 12
SP - 159
EP - 173
JO - IEEE Transactions on Big Data
JF - IEEE Transactions on Big Data
IS - 1
ER -