Evidence map›Paper›PMID 29022896›Full record

ArticleCell death & disease2017

MicroRNA-378 protects against intestinal ischemia/reperfusion injury via a mechanism involving the inhibition of intestinal mucosal cell apoptosis.

Yunsheng Li, Shihong Wen, Xi Yao, Weifeng Liu, Jiantong Shen, Wentao Deng, Jing Tang, Cai Li, Kexuan Liu

Abstract read
In one paragraph

Article in Cell death & disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
–field-weighted citation impact
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

33 citing papers in PubMed.

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  14. Ferroptosis: A Double-Edged Sword in Gastrointestinal Disease.International journal of molecular sciences · 2021
    Review
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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.

Yunsheng LiDepartment of Anesthesiology, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 China.
Shihong WenDepartment of Anesthesiology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China.
Xi YaoDepartment of Anesthesiology, Shaanxi Provincial People's Hospital, Shaanxi 710068, China.
Weifeng LiuDepartment of Anesthesiology, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 China.
Jiantong ShenDepartment of Anesthesiology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China.
Wentao DengDepartment of Anesthesiology, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 China.
Jing TangDepartment of Anesthesiology, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 China.
Cai LiDepartment of Anesthesiology, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 China.
Kexuan LiuDepartment of Anesthesiology, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intestinal ischemia/reperfusion (I/R) injury remains a major clinical event and contributes to high morbidity and mortality rates, but the underlying mechanisms remain elusive. Recent studies have demonstrated that microRNAs (miRNAs) have important roles in organ I/R injury, but the changes and potential roles of miRNAs in intestinal I/R-induced intestinal injury are unclear. This study was designed to analyze the miRNA expression profiles in intestinal mucosa after I/R injury and to explore the role of target miRNA during this process. Using miRNA microarray analysis, we found changes of 19 miRNAs from the expression profile of miRNAs in a mouse model of intestinal I/R and further verified them by RT-qPCR. Here, we report that miR-378 is one of the markedly decreased miRNAs and found the putative target mRNA that is linked to cell death after applying the TargetScan, miRanda, CLIP-Seq and miRDB prediction algorithms. Our results show that the overexpression of miR-378 significantly ameliorated intestinal tissue damage in wild-type and transgenic mice and oxygen glucose deprivation/reperfusion-challenged IEC-6 cell injury. Moreover, miR-378 overexpression reduced intestinal epithelial cell apoptosis in both in vivo and in vitro ischemic models and attenuated cleaved caspase-3 expression. Collectively, our results revealed that the suppression of caspase-3 activation by miRNA-378 overexpression may be involved in the protective effects of intestinal ischemic damage. MiRNA-378 may serve as a key regulator and therapeutic target in intestinal I/R injury.

Indexed as

Amine Oxidase (Copper-Containing)AnimalsApoptosisCaspase 3Cells, CulturedDisease Models, AnimalIntestinal MucosaIschemiaMaleMiceMice, TransgenicMicroRNAsReperfusion InjuryAmine Oxidase (Copper-Containing)Caspase 3MicroRNAsMIRN378 microRNA, mouse

Identifiers

PMID29022896
PMCPMC5682673

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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.