Evidence map›Paper›PMID 31784954›Full record

ArticleHuman cell2020

MiR-216a alleviates LPS-induced acute lung injury via regulating JAK2/STAT3 and NF-κB signaling.

Fanpo Kong, Yanqi Sun, Wenke Song, Yongqin Zhou, Siliang Zhu

Abstract read
PubMed Publisher
In one paragraph

Article in Human cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Pooled it
  2. ACT001 alleviates sepsis-induced acute lung injury by downregulating PANoptosis via the JAK2/STAT3 pathway.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
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  8. IL-6 Mutation Attenuates Liver Injury Caused byInternational journal of molecular sciences · 2023
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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

5 authors at 1 institution in 1 country.

Fanpo KongDepartment of Intensive Care Unit, Tengzhou Central People's Hospital, Tengzhou, 277500, Shandong, People's Republic of China.
Yanqi SunDepartment of Intensive Care Unit, Tengzhou Central People's Hospital, Tengzhou, 277500, Shandong, People's Republic of China.
Wenke SongDepartment of Intensive Care Unit, Tengzhou Central People's Hospital, Tengzhou, 277500, Shandong, People's Republic of China.
Yongqin ZhouDepartment of Intensive Care Unit, Tengzhou Central People's Hospital, Tengzhou, 277500, Shandong, People's Republic of China.
Siliang ZhuDepartment of Intensive Care Unit, Tengzhou Central People's Hospital, Tengzhou, 277500, Shandong, People's Republic of China. tzzhu5637@163.com.ORCID http://orcid.org/0000-0002-8225-0155
Tengzhou Central People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) play an important role in the progression of acute lung injury (ALI) and acute respiratory distress syndrome (ARDS). Till now, little is known about the role of miR-216a in ALI/ARDS. In this study, patients with ARDS exhibited significantly higher interleukin-1β (IL-1β), interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) levels than healthy controls (P < 0.01). However, miR-216a expression in patients with ARDS was significantly lower than healthy controls (P < 0.05), and negatively correlated with 28-day survival rate. Similar effects were observed in LPS-treated mice and A549 cells. MiR-216a over-expression reduced LPS-induced IL-1β, IL-6 and TNF-α levels, and ameliorated lung permeability, and prolonged overall survival of ALI mice. Further, miR-216a over-expression inhibited LPS-induced apoptosis and autophagy. In addition, the janus kinase-2 (JAK2) was a direct target of miR-216a. Silencing of JAK2 partially aggravated miR-216a-inhibited inflammation injury. Besides, miR-216a obviously decreased the expressions of phosphorylated signal transducer and the activator of transcription 3 (p-STAT3), p-p56, and p-IκBα. In conclusion, miR-216a alleviates LPS-induced inflammatory injury via regulating JAK2/STAT3 and NF-κB signaling.

Indexed as

Acute Lung InjuryHumansJanus Kinase 2MicroRNAsNF-kappa BSignal TransductionSTAT3 Transcription FactorJAK2 protein, humanJanus Kinase 2MicroRNAsMIRN216 microRNA, humanNF-kappa BSTAT3 protein, humanSTAT3 Transcription FactorALI/ARDSJAK2LPSmiR-216a

Identifiers

PMID31784954
OpenAlexW2991254950

What OpenQuestion holds

Textmetadata
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.