Evidence map›Paper›PMID 32779953›Full record

ArticleBioengineered2020

Possible role of microRNA miRNA-IL-25 interaction in mice with ulcerative colitis.

Jun Yao, Ruo-Yu Gao, Ming-Han Luo, Cheng Wei, Ben-Hua Wu, Li-Liangzi Guo, Li-Sheng Wang, Jian-Yao Wang, De-Feng Li

Open access · goldAbstract read
In one paragraph

Article in Bioengineered, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 41% 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

5 citing papers in PubMed, 8 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

9 authors at 2 institutions in 1 country.

Jun YaoDepartment of Gastroenterology, Jinan University of Second Clinical Medical Sciences, Shenzhen People's Hospital , Shenzhen, Guangdong Province, China.
Ruo-Yu GaoDepartment of Gastroenterology, Jinan University of Second Clinical Medical Sciences, Shenzhen People's Hospital , Shenzhen, Guangdong Province, China.
Ming-Han LuoDepartment of Gastroenterology, Jinan University of Second Clinical Medical Sciences, Shenzhen People's Hospital , Shenzhen, Guangdong Province, China.
Cheng WeiDepartment of Gastroenterology, Jinan University of Second Clinical Medical Sciences, Shenzhen People's Hospital , Shenzhen, Guangdong Province, China.
Ben-Hua WuDepartment of Gastroenterology, Jinan University of Second Clinical Medical Sciences, Shenzhen People's Hospital , Shenzhen, Guangdong Province, China.
Li-Liangzi GuoDepartment of Gastroenterology, Jinan University of Second Clinical Medical Sciences, Shenzhen People's Hospital , Shenzhen, Guangdong Province, China.
Li-Sheng WangDepartment of Gastroenterology, Jinan University of Second Clinical Medical Sciences, Shenzhen People's Hospital , Shenzhen, Guangdong Province, China.
Jian-Yao WangDepartment of General Surgery, Shenzhen Children's Hospital , Shenzhen, Guangdong Province, China.
De-Feng LiDepartment of Gastroenterology, Jinan University of Second Clinical Medical Sciences, Shenzhen People's Hospital , Shenzhen, Guangdong Province, China.
Jinan University · CNShenzhen Children's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe regulatory network of ulcerative colitis (UC)-associated miRNAs is not fully understood. In this study, we aim to investigate the global profile and regulatory network of UC associated miRNAs in the context of dextran sulfate sodium (DSS).

methodsUC was induced in C57BL mice using DSS. Differentially expressed miRNAs were screened by RNA sequencing and subjected to the Kyoto Encyclopedia of Genes and Genomes Pathway enrichment analysis. RT-qPCR was used to verify the differential expression of miRNAs and candidate target mRNA. Luciferase reporter vector bearing a miRNA binding site was constructed to verify the binding site of the miRNA on mRNA.

resultsA total of 95 miRNAs (31 were up-regulated and 64 were down regulated) differentially expressed in the colonic tissues of the UC mice. Among the differentially expressed miRNAs, IL-25 pathway genes were enriched. Subsequent RT-qPCR confirmed a decreased expression of IL-25 and a significant up regulation of IL-25 target miRNAs including mmu-miR-135b-5p, mmu-miR-7239-5p and mmu-miR-691 in UC mice.

conclusionUsing the luciferase assay, we verified the biding sites of mmu-miR-135b-5p and mmu-miR-691 to the IL-25 3'UTR. In conclusion, mmu-miR-135b-5p:IL-25 and mmu-miR-691:IL-25 interactions are important pathways that may exert a protective role in UC.

Indexed as

AnimalsColitis, UlcerativeInterleukinsMiceMice, Inbred C57BLMicroRNAsRNA, MessengerSequence Analysis, RNAInterleukinsMicroRNAsMirn135 microRNA, mouseMydgf protein, mouseRNA, MessengerIL-25MicroRNAmiR-135b-5pmiR-691ulcerative colitis

Identifiers

PMID32779953
PMCPMC8291871
OpenAlexW3048407803

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.