Dataset Information

Prediction of lncRNA-Disease Associations via Closest Node Weight Graphs of the Spatial Neighborhood Based on the Edge Attention Graph Convolutional Network.

ABSTRACT: Accumulated evidence of biological clinical trials has shown that long non-coding RNAs (lncRNAs) are closely related to the occurrence and development of various complex human diseases. Research works on lncRNA-disease relations will benefit to further understand the pathogenesis of human complex diseases at the molecular level, but only a small proportion of lncRNA-disease associations has been confirmed. Considering the high cost of biological experiments, exploring potential lncRNA-disease associations with computational approaches has become very urgent. In this study, a model based on closest node weight graph of the spatial neighborhood (CNWGSN) and edge attention graph convolutional network (EAGCN), LDA-EAGCN, was developed to uncover potential lncRNA-disease associations by integrating disease semantic similarity, lncRNA functional similarity, and known lncRNA-disease associations. Inspired by the great success of the EAGCN method on the chemical molecule property recognition problem, the prediction of lncRNA-disease associations could be regarded as a component recognition problem of lncRNA-disease characteristic graphs. The CNWGSN features of lncRNA-disease associations combined with known lncRNA-disease associations were introduced to train EAGCN, and correlation scores of input data were predicted with EAGCN for judging whether the input lncRNAs would be associated with the input diseases. LDA-EAGCN achieved a reliable AUC value of 0.9853 in the ten-fold cross-over experiments, which was the highest among five state-of-the-art models. Furthermore, case studies of renal cancer, laryngeal carcinoma, and liver cancer were implemented, and most of the top-ranking lncRNA-disease associations have been proven by recently published experimental literature works. It can be seen that LDA-EAGCN is an effective model for predicting potential lncRNA-disease associations. Its source code and experimental data are available at https://github.com/HGDKMF/LDA-EAGCN.

SUBMITTER: Li J

PROVIDER: S-EPMC8763691 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Project description:It is well known that the unusual expression of long non-coding RNAs (lncRNAs) is closely related to the physiological and pathological processes of diseases. Therefore, inferring the potential lncRNA-disease associations are helpful for understanding the molecular pathogenesis of diseases. Most previous methods have concentrated on the construction of shallow learning models in order to predict lncRNA-disease associations, while they have failed to deeply integrate heterogeneous multi-source data and to learn the low-dimensional feature representations from these data. We propose a method based on the convolutional neural network with the attention mechanism and convolutional autoencoder for predicting candidate disease-related lncRNAs, and refer to it as CNNDLP. CNNDLP integrates multiple kinds of data from heterogeneous sources, including the associations, interactions, and similarities related to the lncRNAs, diseases, and miRNAs. Two different embedding layers are established by combining the diverse biological premises about the cases that the lncRNAs are likely to associate with the diseases. We construct a novel prediction model based on the convolutional neural network with attention mechanism and convolutional autoencoder to learn the attention and the low-dimensional network representations of the lncRNA-disease pairs from the embedding layers. The different adjacent edges among the lncRNA, miRNA, and disease nodes have different contributions for association prediction. Hence, an attention mechanism at the adjacent edge level is established, and the left side of the model learns the attention representation of a pair of lncRNA and disease. A new type of lncRNA similarity and a new type of disease similarity are calculated by incorporating the topological structures of multiple bipartite networks. The low-dimensional network representation of the lncRNA-disease pairs is further learned by the autoencoder based convolutional neutral network on the right side of the model. The cross-validation experimental results confirm that CNNDLP has superior prediction performance compared to the state-of-the-art methods. Case studies on stomach cancer, breast cancer, and prostate cancer further show the ability of CNNDLP for discovering the potential disease lncRNAs.

Project description:BACKGROUND:Automatically extracting relations between chemicals and diseases plays an important role in biomedical text mining. Chemical-disease relation (CDR) extraction aims at extracting complex semantic relationships between entities in documents, which contain intrasentence and intersentence relations. Most previous methods did not consider dependency syntactic information across the sentences, which are very valuable for the relations extraction task, in particular, for extracting the intersentence relations accurately. OBJECTIVE:In this paper, we propose a novel end-to-end neural network based on the graph convolutional network (GCN) and multihead attention, which makes use of the dependency syntactic information across the sentences to improve CDR extraction task. METHODS:To improve the performance of intersentence relation extraction, we constructed a document-level dependency graph to capture the dependency syntactic information across sentences. GCN is applied to capture the feature representation of the document-level dependency graph. The multihead attention mechanism is employed to learn the relatively important context features from different semantic subspaces. To enhance the input representation, the deep context representation is used in our model instead of traditional word embedding. RESULTS:We evaluate our method on CDR corpus. The experimental results show that our method achieves an F-measure of 63.5%, which is superior to other state-of-the-art methods. In the intrasentence level, our method achieves a precision, recall, and F-measure of 59.1%, 81.5%, and 68.5%, respectively. In the intersentence level, our method achieves a precision, recall, and F-measure of 47.8%, 52.2%, and 49.9%, respectively. CONCLUSIONS:The GCN model can effectively exploit the across sentence dependency information to improve the performance of intersentence CDR extraction. Both the deep context representation and multihead attention are helpful in the CDR extraction task.

Dataset Information

Prediction of lncRNA-Disease Associations via Closest Node Weight Graphs of the Spatial Neighborhood Based on the Edge Attention Graph Convolutional Network.

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