Evidence map›Paper›PMID 32146774›Full record

ArticleClinical and experimental reproductive medicine2020

Identification of microRNAs and their target genes in the placenta as biomarkers of inflammation.

Hee Yeon Jang, Seung Mook Lim, Hyun Jung Lee, Joon-Seok Hong, Gi Jin Kim

Open access · diamondAbstract read
In one paragraph

Article in Clinical and experimental reproductive medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 45% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. A Novel Role for Coilin in Vertebrate Innate Immunity.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
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  3. Possible causes of atherosclerosis: lncRNAAnnals of translational medicine · 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

5 authors at 2 institutions in 1 country.

Hee Yeon JangDepartment of Biomedical Science, CHA University, Seongnam, Korea.
Seung Mook LimDepartment of Biomedical Science, CHA University, Seongnam, Korea.
Hyun Jung LeeNon-Clinical Evaluation Center, CHA Advanced Research Institute, Seongnam, Korea.
Joon-Seok HongDepartment of Obstetrics and Gynecology, Seoul National University Bundang Hospital, Seongnam, Korea.
Gi Jin KimDepartment of Biomedical Science, CHA University, Seongnam, Korea.
CHA University · KRSeoul National University Bundang Hospital · KR

Funding

Korea Health Industry Development Institute HI12C768National Research Foundation of Korea 2016M3A9B6903237National Research Foundation of Korea 2018R1A2A3074640
6 · The paper itself

Abstract

objectiveRecently, microRNA (miRNA) has been identified both as a powerful regulator involved in various biological processes through the regulation of numerous genes and as an effective biomarker for the prediction and diagnosis of various disease states. The objective of this study was to identify and validate miRNAs and their target genes involved in inflammation in placental tissue.

methodsMicroarrays were utilized to obtain miRNA and gene expression profiles from placentas with or without inflammation obtained from nine normal pregnant women and 10 preterm labor patients. Quantitative real-time polymerase chain reaction and Western blots were performed to validate the miRNAs and differentially-expressed genes in the placentas with inflammation. Correlations between miRNA and target gene expression were confirmed by luciferase assays in HTR-8/SVneo cells.

resultsWe identified and validated miRNAs and their target genes that were differentially expressed in placentas with inflammation. We also demonstrated that several miRNAs (miR-371a-5p, miR-3065-3p, miR-519b-3p, and miR-373-3p) directly targeted their target genes (LEF1, LOX, ITGB4, and CD44). However, some miRNAs and their direct target genes showed no correlation in tissue samples. Interestingly, miR-373-3p and miR-3065-3p were markedly regulated by lipopolysaccharide (LPS) treatment, although the expression of their direct targets CD44 and LOX was not altered by LPS treatment.

conclusionThese results provide candidate miRNAs and their target genes that could be used as placental biomarkers of inflammation. These candidates may be useful for further miRNA-based biomarker development.

Indexed as

CD44MicroarraymiR-373-3pPreterm labor

Identifiers

PMID32146774
PMCPMC7127901
OpenAlexW3010269743

What OpenQuestion holds

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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.