Evidence map›Paper›PMID 41486996›Full record

ArticleCurrent drug targets2026

RWRGDR: Random Walk and GraphSAGE-based Framework for Enhanced Drug Repositioning.

Biffon Manyura Momanyi, Sebu Aboma Temesgen, Bakanina Kissanga Grace-Mercure, Muhammad Arif, Tanvir Alam, Hui Gao, Li-Xia Tang, Rui-Qin Fang

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Article in Current drug targets, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Biffon Manyura MomanyiSchool of Life Science and Technology, Center for Informational Biology, University of Electronic Science and Technology of China, Chengdu, 610054, China.
Sebu Aboma TemesgenSchool of Life Science and Technology, Center for Informational Biology, University of Electronic Science and Technology of China, Chengdu, 610054, China.
Bakanina Kissanga Grace-MercureSchool of Life Science and Technology, Center for Informational Biology, University of Electronic Science and Technology of China, Chengdu, 610054, China.
Muhammad ArifHamad Bin Khalifa University, Doha, Qatar.
Tanvir AlamHamad Bin Khalifa University, Doha, Qatar.
Hui GaoSchool of Computer Science and Engineering, Center for Informational Biology, University of Electronic Science and Technology of China, Chengdu, China.
Li-Xia TangSchool of Life Science and Technology, Center for Informational Biology, University of Electronic Science and Technology of China, Chengdu, 610054, China.
Rui-Qin FangSchool of Life Science and Technology, Center for Informational Biology, University of Electronic Science and Technology of China, Chengdu, 610054, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDrug development is expensive and time-consuming. Advanced computational methods for mining drug-disease correlations are increasingly popular and gradually replacing traditional biological experiments. However, most existing techniques rely primarily on network information. They do not fully leverage integration details and rarely capitalize on drug-disease associations. This study proposes the RWRGDR framework, which uses Graph Neural Networks (GNN) for unsupervised feature learning to identify potential drug-disease interactions. The Random Walk with Restart (RWR) algorithm serves as a complementary mechanism to enhance prediction performance.

methodsThe GraphSAGE algorithm first encodes low-dimensional representations, leveraging GAT for multi-head attention to weight the significance of neighbors. The RWR algorithm then captures the global network perspective from a given target node, complementing the initial embeddings with global topological descriptors. This convex integration fuses local features and long-range dependencies, ultimately leading to superior downstream predictions.

resultsOur model, based on the Multilayer Perceptron (MLP) classifier, achieved outstanding performance, with Area Under the Curve (AUC) and Area Under the Precision-Recall Curve (AUPRC) values of 0.84 and 0.91, respectively. This performance is highly competitive, surpassing previous techniques. Case studies validate its practical applicability. DISCUSSION: Comprehensive network exploration facilitates an in-depth understanding of complex interactions and extracts meaningful insights required for optimized predictions. Despite a relatively lower AUC, our model outperformed prior methods in AUPRC, highlighting its ability to prioritize highly ranked minority positives.

conclusionRWRGDR represents a potentially reliable drug repositioning strategy, as demonstrated through case studies, indicating its practical significance, particularly for emerging conditions with no recognized treatments.

Indexed as

Drug RepositioningAlgorithmsComputational BiologyData MiningGraph Neural NetworksHumansMultilayer PerceptronsPrediction AlgorithmsDrug repositioninggraph neural networksGraphSAGEprecision medicinerandom walk with restart

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.