Evidence map›Paper›PMID 31915414›Full record

ArticleMediators of inflammation2019

miR-657 Promotes Macrophage Polarization toward M1 by Targeting FAM46C in Gestational Diabetes Mellitus.

Pingping Wang, Zengfang Wang, Guojie Liu, Chengwen Jin, Quan Zhang, Shuhong Man, Zengyan Wang

Open access · goldAbstract read
In one paragraph

Article in Mediators of inflammation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
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  5. The role of microRNAs in pregnancies complicated by maternal diabetes.Clinical science (London, England : 1979) · 2024
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  20. The Mystery of Exosomes in Gestational Diabetes Mellitus.Oxidative medicine and cellular longevity · 2022
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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 4 institutions in 1 country.

Pingping WangDepartment of Gynecology and Obstetrics, Weifang Hospital of Maternal and Child Health, Weifang 261000, China.ORCID https://orcid.org/0000-0003-1878-2410
Zengfang WangDepartment of Gynecology and Obstetrics, Weifang Hospital of Maternal and Child Health, Weifang 261000, China.
Guojie LiuDepartment of Gynecology and Obstetrics, Weifang Hospital of Maternal and Child Health, Weifang 261000, China.
Chengwen JinFunctional Laboratory, Clinical Medicine College of Weifang Medical University, Weifang 261000, China.
Quan ZhangDepartment of Cardiology, Clinical Medicine College, Weifang Medical University, Weifang 261000, China.
Shuhong ManDepartment of Gynecology, People's Hospital of Weifang, Weifang 261000, China.ORCID https://orcid.org/0000-0003-2648-4480
Zengyan WangOperating Room, Zhucheng People's Hospital, Zhucheng 262200, China.ORCID https://orcid.org/0000-0002-9903-7967
Weifang Maternity and Child Care Hospital · CNWeifang Medical University · CNZoucheng People's Hospital · CNWeifang People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNA (miRNA) has been widely suggested to play a vital role of in the pathogenesis of gestational diabetes mellitus (GDM). We have previously demonstrated that miR-657 can regulate macrophage inflammatory response in GDM. However, the role of miR-657 on M1/M2 macrophage polarization in GDM pathogenesis is not clear yet. This study is aimed at elucidating this issue and identifying novel potential GDM therapeutic targets based on miRNA network. miR-657 is found to be upregulated in placental macrophages demonstrated by real-time PCR, which can enhance macrophage proliferation and migration in vitro. Luciferase reporter assay shows the evidence that FAM46C is a target of miR-657. In addition, miR-657 can promote macrophage polarization toward the M1 phenotype by downregulating FAM46C in macrophages. The present study strongly suggests miR-657 is involved in GDM pathogenesis by regulating macrophage proliferation, migration, and polarization via targeting FAM46C. miR-657/FAM46C may serve as promising targets for GDM diagnosis and treatment.

Indexed as

AdultBlotting, WesternCell MovementCell ProliferationDiabetes, GestationalFemaleFluorescent Antibody TechniqueHumansMacrophage ActivationMicroRNAsNucleotidyltransferasesPregnancyReal-Time Polymerase Chain ReactionTHP-1 CellsMicroRNAsMIRN657 microRNA, humanNucleotidyltransferasesTENT5C protein, human

Identifiers

PMID31915414
PMCPMC6930733
OpenAlexW2995869873

What OpenQuestion holds

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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 OpenQuestion graph.