Evidence map›Paper›PMID 35889243›Full record

ArticleMolecules (Basel, Switzerland)2022

TLNPMD: Prediction of miRNA-Disease Associations Based on miRNA-Drug-Disease Three-Layer Heterogeneous Network.

Yi Yang, Junliang Shang, Yan Sun, Feng Li, Yuanyuan Zhang, Xiang-Zhen Kong, Shengjun Li, Jin-Xing Liu

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 51% of its field
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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 2 institutions in 1 country.

Yi YangSchool of Computer Science, Qufu Normal University, Rizhao 276826, China.
Junliang ShangSchool of Computer Science, Qufu Normal University, Rizhao 276826, China.ORCID 0000-0002-8488-2228
Yan SunSchool of Computer Science, Qufu Normal University, Rizhao 276826, China.
Feng LiSchool of Computer Science, Qufu Normal University, Rizhao 276826, China.
Yuanyuan ZhangSchool of Information and Control Engineering, Qingdao University of Technology, Qingdao 266520, China.
Xiang-Zhen KongSchool of Computer Science, Qufu Normal University, Rizhao 276826, China.
Shengjun LiSchool of Computer Science, Qufu Normal University, Rizhao 276826, China.
Jin-Xing LiuSchool of Computer Science, Qufu Normal University, Rizhao 276826, China.
Qufu Normal University · CNQingdao University of Technology · CN

Funding

Project of Shandong Province Higher Educational Science and Technology Program J18KA373the National Science Foundation of China 61972226, 61902216, 61902430, 61702299, 61872220
6 · The paper itself

Abstract

Many microRNAs (miRNAs) have been confirmed to be associated with the generation of human diseases. Capturing miRNA-disease associations (M-DAs) provides an effective way to understand the etiology of diseases. Many models for predicting M-DAs have been constructed; nevertheless, there are still several limitations, such as generally considering direct information between miRNAs and diseases, usually ignoring potential knowledge hidden in isolated miRNAs or diseases. To overcome these limitations, in this study a novel method for predicting M-DAs was developed named TLNPMD, highlights of which are the introduction of drug heuristic information and a bipartite network reconstruction strategy. Specifically, three bipartite networks, including drug-miRNA, drug-disease, and miRNA-disease, were reconstructed as weighted ones using such reconstruction strategy. Based on these weighted bipartite networks, as well as three corresponding similarity networks of drugs, miRNAs and diseases, the miRNA-drug-disease three-layer heterogeneous network was constructed. Then, this heterogeneous network was converted into three two-layer heterogeneous networks, for each of which the network path computational model was employed to predict association scores. Finally, both direct and indirect miRNA-disease paths were used to predict M-DAs. Comparative experiments of TLNPMD and other four models were performed and evaluated by five-fold and global leave-one-out cross validations, results of which show that TLNPMD has the highest AUC values among those of compared methods. In addition, case studies of two common diseases were carried out to validate the effectiveness of the TLNPMD. These experiments demonstrate that the TLNPMD may serve as a promising alternative to existing methods for predicting M-DAs.

Indexed as

MicroRNAsAlgorithmsComputational BiologyHumansMicroRNAsdrug heuristic informationmiRNA-diseasenetwork paththree-layer heterogeneous

Identifiers

PMID35889243
PMCPMC9324587
OpenAlexW4284880725

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.