IEEE J Biomed Health Inform. 2024 Jul;28(7):4306-4316. doi: 10.1109/JBHI.2024.3397003. Epub 2024 Jul 2.
Dysregulation of miRNAs is closely related to the progression of various diseases, so identifying disease-related miRNAs is crucial. Most recently proposed methods are based on graph reasoning, while they did not completely exploit the topological structure composed of the higher-order neighbor nodes and the global and local features of miRNA and disease nodes. We proposed a prediction method, MDAP, to learn semantic features of miRNA and disease nodes based on various meta-paths, as well as node features from the entire heterogeneous network perspective, and node pair attributes. Firstly, for both the miRNA and disease nodes, node category-wise meta-paths were constructed to integrate the similarity and association connection relationships. Each target node has its specific neighbor nodes for each meta-path, and the neighbors of longer meta-paths constitute its higher-order neighbor topological structure. Secondly, we constructed a meta-path specific graph convolutional network module to integrate the features of higher-order neighbors and their topology, and then learned the semantic representations of nodes. Thirdly, for the entire miRNA-disease heterogeneous network, a global-aware graph convolutional autoencoder was built to learn the network-view feature representations of nodes. We also designed semantic-level and representation-level attentions to obtain informative semantic features and node representations. Finally, the strategy based on the parallel convolutional-deconvolutional neural networks were designed to enhance the local feature learning for a pair of miRNA and disease nodes. The experiment results showed that MDAP outperformed other state-of-the-art methods, and the ablation experiments demonstrated the effectiveness of MDAP's major innovations. MDAP's ability in discovering potential disease-related miRNAs was further analyzed by the case studies over three diseases.
miRNA 的失调与各种疾病的进展密切相关,因此识别与疾病相关的 miRNA 至关重要。最近提出的大多数方法都是基于图推理的,而这些方法并没有完全利用由高阶邻节点以及 miRNA 和疾病节点的全局和局部特征组成的拓扑结构。我们提出了一种预测方法 MDAP,该方法基于各种元路径学习 miRNA 和疾病节点的语义特征,以及从整个异构网络角度的节点特征和节点对属性。首先,对于 miRNA 和疾病节点,构建节点类别特定的元路径,以整合相似性和关联连接关系。对于每个元路径,每个目标节点都有其特定的邻居节点,而较长元路径的邻居则构成其高阶邻拓扑结构。其次,我们构建了一个特定于元路径的图卷积网络模块,以整合高阶邻居及其拓扑的特征,然后学习节点的语义表示。第三,对于整个 miRNA-疾病异构网络,构建了一个全局感知图卷积自动编码器,以学习节点的网络视图特征表示。我们还设计了语义级和表示级注意力机制,以获取信息丰富的语义特征和节点表示。最后,设计了基于并行卷积-反卷积神经网络的策略,以增强对 miRNA 和疾病节点对的局部特征学习。实验结果表明,MDAP 优于其他最先进的方法,消融实验证明了 MDAP 的主要创新的有效性。通过对三种疾病的案例研究,进一步分析了 MDAP 发现潜在疾病相关 miRNA 的能力。