Evidence map›Paper›PMID 37782276›Full record

ArticleRenal failure2023

CircRNA itchy E3 ubiquitin protein ligase improves mitochondrial dysfunction in sepsis-induced acute kidney injury by targeting microRNA-214-3p/ATP-binding cassette A1 axis.

Weidi Ye, Qi Miao, Guangxin Xu, Kai Jin, Xue Li, Weidong Wu, Lina Yu, Min Yan

Open access · goldAbstract read
In one paragraph

Article in Renal failure, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
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  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. The roles of the ubiquitin-proteasome system in renal disease.International journal of medical sciences · 2025
    Review
  10. Article
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

8 authors at 1 institution in 1 country.

Weidi YeDepartment of Anesthesiology, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, P.R. China.
Qi MiaoZhejiang Provincial Engineering Institute on Eye Diseases, Zhejiang Provincial Key Laboratory of Ophthalmology, Zhejiang Provincial Clinical Research Center for Eye Diseases, Eye Center Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, P.R. China.
Guangxin XuDepartment of Anesthesiology, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, P.R. China.
Kai JinZhejiang Provincial Engineering Institute on Eye Diseases, Zhejiang Provincial Key Laboratory of Ophthalmology, Zhejiang Provincial Clinical Research Center for Eye Diseases, Eye Center Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, P.R. China.
Xue LiDepartment of Anesthesiology, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, P.R. China.
Weidong WuDepartment of Anesthesiology, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, P.R. China.
Lina YuDepartment of Anesthesiology, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, P.R. China.
Min YanDepartment of Anesthesiology, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, P.R. China.
Second Affiliated Hospital of Zhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCircular RNAs (circRNAs) are promising biomarkers and therapeutic targets for acute kidney injury (AKI). In this study, we investigated the mechanism by which circRNA itchy E3 ubiquitin protein ligase (circ-ITCH) regulates sepsis-induced AKI.

methodsA sepsis-induced AKI mouse model was created using LPS induction and circ-ITCH overexpression. Circ-ITCH levels were confirmed

resultsCirc-ITCH expression was downregulated in LPS-induced sepsis mice. Overexpression of circ-ITCH ameliorates indicators of renal function (serum creatinine [SCr], blood urea nitrogen [BUN], neutrophil gelatinase-associated lipocalin [NGAL], and kidney injury molecule-1 [Kim-1]), reduces renal cell apoptosis, mitigates oxidative stress markers (reactive oxygen species [ROS] and malondialdehyde [MDA]), and diminishes inflammatory markers (interleukin [IL]-1β, IL-6, and tumor necrosis factor [TNF-α]). Moreover, circ-ITCH overexpression alleviated mitochondrial damage and dysfunction. Furthermore, circ-ITCH acts as a sponge for miR-214-3p, thereby upregulating ABCA1 expression. In addition, the miR-214-3p inhibitor repressed oxidative stress, inflammation, and mitochondrial dysfunction, which was reversed by circ-ITCH knockdown. Further cellular analysis in HK-2 cells supported these findings, highlighting the protective role of circ-ITCH against sepsis-induced AKI, particularly through the miR-214-3p/ABCA1 axis.

conclusionThe novel circ-ITCH/miR-214-3p/ABCA1 pathway plays an essential role in the regulation of oxidative stress and mitochondrial dysfunction in sepsis-induced AKI.

Indexed as

Acute Kidney InjuryMicroRNAsRNA, CircularSepsisAdenosine TriphosphateAnimalsApoptosisATP Binding Cassette Transporter 1LipopolysaccharidesMiceMitochondriaUbiquitin-Protein LigasesAbca1 protein, mouseAdenosine TriphosphateATP Binding Cassette Transporter 1Itch protein, mouseLipopolysaccharidesMicroRNAsMirn214 microRNA, mouseRNA, CircularUbiquitin-Protein LigasesABCA1circ-ITCHmicroRNA-214-3pmitochondrial dysfunctionsepsis-induced acute kidney injury

Identifiers

PMID37782276
PMCPMC10547449
OpenAlexW4387241762

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.