Evidence map›Paper›PMID 32412059›Full record

ArticleBioscience reports2020

MiR-22-3p suppresses sepsis-induced acute kidney injury by targeting PTEN.

Xudong Wang, Yali Wang, Mingjian Kong, Jianping Yang

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
5.7field-weighted citation impact, top 3% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 64 citations in OpenAlex.

  1. Pooled it
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  13. MicroRNA Profiles in Critically Ill Patients.Current medicinal chemistry · 2024
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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

4 authors at 2 institutions in 1 country.

Xudong WangDepartment of Anesthesiology, Affiliated First Hospital, Soochow University, Suzhou, China.
Yali WangDepartment of Anesthesiology, the Second Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Mingjian KongDepartment of Anesthesiology, the Second Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Jianping YangDepartment of Anesthesiology, Affiliated First Hospital, Soochow University, Suzhou, China.
Soochow University · CNXuzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSeptic acute kidney injury is considered as a severe and frequent complication that occurs during sepsis. The present study was performed to understand the role of miR-22-3p and its underlying mechanism in sepsis-induced acute kidney injury.

methodsRats were injected with adenovirus carrying miR-22-3p or miR-NC in the caudal vein before cecal ligation. Meanwhile, HK-2 cells were transfected with the above adenovirus following LPS stimulation. We measured the markers of renal injury (blood urea nitrogen (BUN), serum creatinine (SCR)). Histological changes in kidney tissues were examined by hematoxylin and eosin (H&E), Masson staining, periodic acid Schiff staining and TUNEL staining. The levels of IL-1β, IL-6, TNF-α and NO were determined by ELISA assay. Using TargetScan prediction and luciferase reporter assay, we predicted and validated the association between PTEN and miR-22-3p.

resultsOur data showed that miR-22-3p was significantly down-regulated in a rat model of sepsis-induced acute kidney injury, in vivo and LPS-induced sepsis model in HK-2 cells, in vitro. Overexpression of miR-22-3p remarkably suppressed the inflammatory response and apoptosis via down-regulating HMGB1, p-p65, TLR4 and pro-inflammatory factors (IL-1β, IL-6, TNF-α and NO), both in vivo and in vitro. Moreover, PTEN was identified as a target of miR-22-3p. Furthermore, PTEN knockdown augmented, while overexpression reversed the suppressive role of miR-22-3p in LPS-induced inflammatory response.

conclusionsOur results showed that miR-22-3p induced protective role in sepsis-induced acute kidney injury may rely on the repression of PTEN.

Indexed as

Acute Kidney InjuryAnimalsApoptosisBlood Urea NitrogenCell LineCreatinineCytokinesDisease Models, AnimalDown-RegulationHumansKidneyLipopolysaccharidesMaleMicroRNAsPTEN PhosphohydrolaseRats, Sprague-DawleyCreatinineCytokineslipopolysaccharide, E coli O55-B5LipopolysaccharidesMicroRNAsMIRN22 microRNA, humanMIRN22 microRNA, ratPTEN PhosphohydrolasePTEN protein, humanPten protein, ratacute kidney injurymiR-22-3pnflammationPTENsepsis

Identifiers

PMID32412059
PMCPMC7268257
OpenAlexW3026879754

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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.