Evidence map›Paper›PMID 35365456›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2022

[Differential expression profile of miRNAs in amniotic fluid exosomes from fetuses with Down syndrome].

K Ding, L Yu, Z Huang, H Zheng, X Yang, T Tian, R Xie

Open access · greenAbstract read
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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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 1 institution in 1 country.

K DingDepartment of Pathophysiology, Guizhou Medical University, Guiyang 550025, China.
L YuDepartment of Pathology, Guiyang Maternal and Child Health Care Center, Guiyang 550003, China.
Z HuangDepartment of Eugenic Genetics, Guiyang Maternal and Child Health Care Center, Guiyang 550003, China.
H ZhengDepartment of Eugenic Genetics, Guiyang Maternal and Child Health Care Center, Guiyang 550003, China.
X YangDepartment of Eugenic Genetics, Guiyang Maternal and Child Health Care Center, Guiyang 550003, China.
T TianDepartment of Eugenic Genetics, Guiyang Maternal and Child Health Care Center, Guiyang 550003, China.
R XieDepartment of Pathophysiology, Guizhou Medical University, Guiyang 550025, China.
Guiyang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the role of miRNAs in amniotic fluid exosomes in growth and development of fetuses with Down syndrome (DS).

methodsAmniotic fluid were collected from 20 fetuses with DS and 20 normal fetuses (control) to extract amniotic exosome miRNA. MicroRNA sequencing technique was used to identify the differentially expressed miRNAs between the two groups, for which gene ontology (GO) and pathway analysis was performed. Three differentially expressed miRNAs with the strongest correlation with DS phenotype were selected for qPCR verification. Dual luciferase reporter assay was used to verify the activity of let-7d-5p for targeted regulation of BACH1.

resultsWe identified 15 differentially expressed miRNAs in DS as compared with the control group, among which 7 miRNAs were up-regulated and 8 were down-regulated. Target gene prediction results showed that the differentially expressed miRNAs targeted 17 DS-related genes. GO analysis revealed that the main functions of the target genes involved protein binding, protein transport, ATP binding, transferase activity and synapses. Pathway analysis revealed that the functional pathways were closely related with the development of the nervous system. qPCR results showed that the expression levels of miR-140-3p and let-7d-5p were significantly lower in DS group than in the control group (

conclusionLet-7d-5p in amniotic fluid exosomes may promote oxidative stress events in the brain of fetuses with DS by regulating BACH1 expression.

Indexed as

Down SyndromeExosomesMicroRNAsAmniotic FluidFemaleHumansPregnancyMicroRNAsMirn140 microRNA, humanamniotic fluidDown syndromeexosomesmiRNA

Identifiers

PMID35365456
PMCPMC8983360
OpenAlexW4223996104

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.