Evidence map›Paper›PMID 26859886›Full record

ArticlePloS one2016

Global MicroRNA Expression Profiling of Mouse Livers following Ischemia-Reperfusion Injury at Different Stages.

Weisheng Zheng, Hewei Men, Jing Li, Yu Xing, Bin Wu, Zhenglu Wang, Junjie Li, Dahong Teng, Yuan Shi, Jiang Li and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Novel Targets for Treating Ischemia-Reperfusion Injury in the Liver.International journal of molecular sciences · 2018
    Review
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

12 authors at 3 institutions in 1 country.

Weisheng ZhengDepartment of Transplant Surgery, Tianjin First Central Hospital, Tianjin, China.
Hewei MenDepartment of Transplant Surgery, Tianjin First Central Hospital, Tianjin, China.
Jing LiDepartment of Gastroenterology, Tianjin First Central Hospital, Tianjin, China.
Yu XingDepartment of Transplant Surgery, Tianjin First Central Hospital, Tianjin, China.
Bin WuDepartment of Transplant Surgery, Tianjin First Central Hospital, Tianjin, China.
Zhenglu WangDepartment of Transplant Surgery, Tianjin First Central Hospital, Tianjin, China.
Junjie LiDepartment of Transplant Surgery, Tianjin First Central Hospital, Tianjin, China.
Dahong TengDepartment of Transplant Surgery, Tianjin First Central Hospital, Tianjin, China.
Yuan ShiDepartment of Transplant Surgery, Tianjin First Central Hospital, Tianjin, China.
Jiang LiDepartment of Transplant Surgery, Tianjin First Central Hospital, Tianjin, China.
Pu JiangDepartment of Forensic Medicine, College of Basic Medicine, Chongqing Medical University, Chongqing, China.
Jinzhen CaiDepartment of Transplant Surgery, Tianjin First Central Hospital, Tianjin, China.
Tianjin First Center Hospital · CNTianjin Medical University · CNChongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatic ischemia-reperfusion injury is a dynamic process consisting of two stages: ischemia and reperfusion, and triggers a cascade of physiological and biochemical events. Given the important role of microRNAs in regulating gene expression, we analyzed gene expression changes in mouse livers at sham control, ischemia stage, and reperfusion stage. We generated global expression profiles of microRNA and mRNA genes in mouse livers subjected to ischemia-reperfusion injury at the three stages, respectively. Comparison analysis showed that reperfusion injury had a distinct expression profile whereas the ischemia sample and the sham control were clustered together. Consistently, there are 69 differentially expressed microRNAs between the reperfusion sample and the sham control whereas 28 differentially expressed microRNAs between the ischemia sample and the sham control. We further identified two modes of microRNA expression changes in ischemia-reperfusion injury. Functional analysis of both the differentially expressed microRNAs in the two modes and their target mRNAs revealed that ischemia injury impaired mitochondrial function, nutrient consumption, and metabolism process. In contrast, reperfusion injury led to severe tissue inflammation that is predominantly an innate-immune response in the ischemia-reperfusion process. Our staged analysis of gene expression profiles provides new insights into regulatory mechanisms of microRNAs in mouse hepatic IR injury.

Indexed as

AnimalsDisease Models, AnimalGene Expression ProfilingGene Regulatory NetworksIschemiaLiverMaleMiceMice, Inbred C57BLMicroRNAsOligonucleotide Array Sequence AnalysisReperfusion InjuryMicroRNAs

Identifiers

PMID26859886
PMCPMC4747576
OpenAlexW2263593807

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.