Evidence map›Paper›PMID 32342116›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2020

SIKIAT1/miR-96/FOXA1 axis regulates sepsis-induced kidney injury through induction of apoptosis.

Shijun Lu, Haibin Wu, Jianhua Xu, Zhaofeng He, Haiyan Li, Chao Ning

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. HNF3α Targets Nckap1l and Promotes Renal Fibrosis Following Ischemia-Reperfusion Injury.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Annexin A1 (Ac2-26)-dependent Fpr2 receptor alleviates sepsis-induced acute kidney injury by inhibiting inflammation and apoptosis in vivo and in vitro.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Non-Coding RNAs in Kidney Diseases: The Long and Short of Them.International journal of molecular sciences · 2021
    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

6 authors at 3 institutions in 1 country.

Shijun LuDepartment of Critical Care Medicine, Shandong Province Linyi Central Hospital, Shandong, China. lushijun2020@126.com.
Haibin WuDepartment of Critical Care Medicine, The Affiliated Hospital of Guangdong Medical College, Guangdong, China.
Jianhua XuDepartment of Critical Care Medicine, Shandong Province Linyi Central Hospital, Shandong, China.
Zhaofeng HeDepartment of Critical Care Medicine, Shandong Province Juxian People's Hospital, Shandong, China.
Haiyan LiDepartment of Critical Care Medicine, Shandong Province Linyi Central Hospital, Shandong, China.
Chao NingDepartment of Critical Care Medicine, Shandong Province Linyi Central Hospital, Shandong, China.
Linyi People's Hospital · CNGuangdong Medical College · CNYuxian People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

OBJECTIVE AND

designNowadays, sepsis-induced acute kidney injury (AKI) has gradually become a global problem for its high incidence and increasing mortality. Previous study has reported lncRNA ENST00000452391.1 in sepsis patients. However, its potential biological function and downstream molecular mechanism are still mysterious. METHODS AND 

resultsOur study found that it was upregulated in sepsis-induced AKI patients, so it was identified as "sepsis-induced kidney injury associated transcript 1 (SIKIAT1)". We used lipopolysaccharide (LPS) stimulated HK-2 cells as an in vitro model to demonstrated that SIKIAT1 acts as a ceRNA for miR-96-3p to enhance FOXA1 expression and promote HK-2 cell apoptosis.

conclusionTherefore, it could be a potential biomarker and therapeutic target for sepsis-induced AKI in the development of disease.

Indexed as

ApoptosisCell LineGene Expression RegulationGene Knockdown TechniquesHepatocyte Nuclear Factor 3-alphaHumansKidneyKidney DiseasesLipopolysaccharidesMicroRNAsRNA, Long NoncodingSepsisTransfectionFOXA1 protein, humanHepatocyte Nuclear Factor 3-alphaLipopolysaccharidesMicroRNAsMIRN96 microRNA, humanRNA, Long NoncodingAKIlncRNAmiRNASepsis

Identifiers

PMID32342116
OpenAlexW3020639193

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.