Evidence map›Paper›PMID 27636999›Full record

ArticleOncotarget2016

Toll-like 4 receptor /NFκB inflammatory/miR-146a pathway contributes to the ART-correlated preterm birth outcome.

Xinqi Zhong, Yi-Zhou Jiang, Peiwen Liu, Wenzhi He, Zhongtang Xiong, Weijie Chang, Jiandong Zhu, Qiliang Cui

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

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  5. Association of Polymorphisms inDisease markers · 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

8 authors at 4 institutions in 1 country.

Xinqi ZhongDepartment of Pediatrics, the Third Affiliated Hospital of Guangzhou Medical University, Guangdong, China.
Yi-Zhou JiangInstitute for Advanced Study, Shenzhen University, Shenzhen, Guangdong, China.
Peiwen LiuDepartment of Pathogen Biology, School of Public Health and Tropical Medicine, Southern Medical University, Guangdong, China.
Wenzhi HeExperimental Department of Institute of Gynecology and Obstetrics, The Third Affiliated Hospital of Guangzhou Medical University, Guangdong, China.
Zhongtang XiongDepartment of Pathology, The Third Affiliated Hospital of Guangzhou Medical University, Guangdong, China.
Weijie ChangDepartment of Pediatrics, the Third Affiliated Hospital of Guangzhou Medical University, Guangdong, China.
Jiandong ZhuDepartment of Pediatrics, the Third Affiliated Hospital of Guangzhou Medical University, Guangdong, China.
Qiliang CuiDepartment of Pediatrics, the Third Affiliated Hospital of Guangzhou Medical University, Guangdong, China.
Guangzhou Medical University · CNThird Affiliated Hospital of Guangzhou Medical University · CNShenzhen University · CNSouthern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Assisted reproductive technology (ART) is widely used for the women with infertility conditions to achieve pregnancy. However, the adverse effects of ART may lead to poor perinatal and neonatal outcomes, e.g., preterm birth and low body weight. In this study, we investigated the inflammatory molecular factors and microRNA that might be involved in ART related preterm birth. We found the elevation of Toll-like 4 receptor (TLR4), activation of NFκB pathway and down-regulation of microRNA-146a (miR-146a), a negative regulator of NFκB, in the placenta of preterm birth and ART, indicating preterm birth and ART were associated with inflammation signaling activation. In vitro experiments demonstrated that miR-146a suppressed NFκB pathway and shifted the balance of cytokines in the cord blood toward a repertoire of pro-inflammatory outcomes by down-regulating IRAK1 and TRAF6. The pro-inflammatory cytokines IL-6, IFNγ and TNFα in the cord blood were highly expressed in the preterm and ART, while anti-inflammatory cytokine IL-10 was the lower in the preterm and ART. In summary, we firstly uncovered that TLR4/NFκB mediated inflammation signaling and miR-146a participated in ART-related preterm birth patients, which suggests that importance of TLR4/NFκB/miR-146a signaling in clinical interventions and biomarkers of ART-related perinatal or neonatal outcomes.

Indexed as

AdultFemaleHumansImmunohistochemistryMicroRNAsNF-kappa BPlacentaPregnancyPremature BirthReproductive Techniques, AssistedSignal TransductionToll-Like Receptor 4TransfectionMicroRNAsMIRN146 microRNA, humanNF-kappa BTLR4 protein, humanToll-Like Receptor 4assisted reproductive technologyinflammatorymiR-146aNFκBPathology Sectionpreterm birthToll-Like 4 receptor

Identifiers

PMID27636999
PMCPMC5341923
OpenAlexW2518902341

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.