Evidence mapPaperPMID 32210913Full record

ArticleFrontiers in endocrinology2020

Construction of Glycometabolism- and Hormone-Related lncRNA-Mediated Feedforward Loop Networks Reveals Global Patterns of lncRNAs and Drug Repurposing in Gestational Diabetes.

Xuelian Fu, Huifang Cong, Shuyu Zhao, Yan Li, Tianyi Liu, Yuhong Sun, Nan Lv

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Xuelian FuDepartment of Endocrinology, Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Huifang CongDepartment of Gynecology, Second Affiliated Hospital of Heilongjiang University of Chinese Medicine, Harbin, China.
Shuyu ZhaoThird Ward of Obstetrics and Gynecology, Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Yan LiThird Ward of Obstetrics and Gynecology, Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Tianyi LiuThird Ward of Obstetrics and Gynecology, Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Yuhong SunThird Ward of Obstetrics and Gynecology, Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Nan LvThird Ward of Obstetrics and Gynecology, Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Harbin Medical University · CNHeilongjiang University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gestational diabetes mellitus (GDM) is a condition associated with the onset of abnormal glucose tolerance during pregnancy. Long non-coding RNAs (lncRNAs), microRNAs (miRNAs), and genes can form lncRNA-mediated feedforward loops (lnc-FFLs), which are functional network motifs that regulate a wide range of biological processes and diseases. However, lnc-FFL network motifs have not been systematically investigated in GDM, and their role in the disease remains largely unknown. In the present study, a global lnc-FFL network was constructed and analyzed. Glycometabolism- and hormone-related lnc-FFL networks were extracted from the global network. An integrated algorithm was designed to identify dysregulated glycometabolism- and hormone-related lnc-FFLs in GDM. The patterns of dysregulated lnc-FFLs in GDM were complex. Moreover, there were strong associations between dysregulated glycometabolism- and hormone-related lnc-FFLs in GDM. Core modules were extracted from the dysregulated lnc-FFL networks in GDM and showed specific and essential functions. In addition, dysregulated lnc-FFLs could combine with ceRNAs and form more complex modules, which could play novel roles in GDM. Notably, we discovered that the dysregulated lnc-FFLs were enriched in the thyroid hormone signaling pathway. Some drug-repurposing candidates, such as hormonal drugs, could be identified based on lnc-FFLs in GDM. In summary, the present study highlighted the effect of dysregulated glycometabolism- and hormone-related lnc-FFLs in GDM and revealed their potential for the discovery of novel biomarkers and therapeutic targets for GDM.

Indexed as

Drug RepositioningFeedback, PhysiologicalBiomarkersDiabetes, GestationalFemaleGene Expression ProfilingGene Regulatory NetworksGlucoseHormonesHumansMicroRNAsPregnancyRNA, Long NoncodingSignal TransductionBiomarkersGlucoseHormonesMicroRNAsRNA, Long Noncodingdrug repurposinggestational diabetesglycometabolismhormonelncRNA-mediated feedforward loopthyroid hormone

Identifiers

PMID32210913
PMCPMC7068675
OpenAlexW3009295471

What Socratic holds

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LicenceCC BY
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Registered trials

None linked

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 Socratic graph.