Evidence map›Paper›PMID 34916780›Full record

ArticleDrug design, development and therapy2021

Knockdown of TRIM8 Protects HK-2 Cells Against Hypoxia/Reoxygenation-Induced Injury by Inhibiting Oxidative Stress-Mediated Apoptosis and Pyroptosis via PI3K/Akt Signal Pathway.

Bang-Hua Zhang, Hao Liu, Yan Yuan, Xiao-Dong Weng, Yang Du, Hui Chen, Zhi-Yuan Chen, Lei Wang, Xiu-Heng Liu

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

18 citing papers in PubMed, 39 citations in OpenAlex.

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  9. The Antioxidant Action ofMolecules (Basel, Switzerland) · 2024
    Review
  10. Review
  11. Article
  12. Review
  13. The Role of Pyroptosis in the Pathogenesis of Kidney Diseases.Kidney diseases (Basel, Switzerland) · 2023
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

9 authors at 1 institution in 1 country.

Bang-Hua ZhangDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, People's Republic of China.ORCID 0000-0003-4367-901X
Hao LiuDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, People's Republic of China.ORCID 0000-0003-1938-8925
Yan YuanDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, People's Republic of China.
Xiao-Dong WengDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, People's Republic of China.
Yang DuDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, People's Republic of China.ORCID 0000-0002-3803-8245
Hui ChenDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, People's Republic of China.
Zhi-Yuan ChenDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, People's Republic of China.
Lei WangDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, People's Republic of China.
Xiu-Heng LiuDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, People's Republic of China.
Wuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute kidney injury (AKI) emerges as an acute and critical disease. Tripartite motif 8 (TRIM8), one number of the TRIM protein family, is proved to participate in ischemia/reperfusion (I/R) injury. However, whether TRIM8 is involved in renal I/R injury and the associated mechanisms are currently unclear. PURPOSE: This study aimed to investigate the precise role of TRIM8 and relevant mechanisms in renal I/R injury. MATERIALS AND

methodsIn this study, human renal proximal tubular epithelial cells (HK-2 cells) underwent 12 hours of hypoxia and 2 h, 3 h or 4 h of reoxygenation to establish an in vitro hypoxia/reoxygenation (H/R) model. The siRNAs specific to TRIM8 (si-TRIM8) were transfected into HK-2 cells to knockdown TRIM8. The cell H/R model included various groups including Control, H/R, H/R+DMSO, H/R+NAC, si-NC+H/R, si-TRIM8+H/R and si-TRIM8+LY294002+H/R. The cell viability and levels of reactive oxygen species (ROS), hydrogen peroxide (H

resultsIn vitro, realtime-quantitative PCR and western-blot analysis showed that the mRNA and protein expression of TRIM8 were obviously upregulated after H/R treatment in HK-2 cells. Compared with the H/R model group, knockdown of TRIM8 significantly increased cell viability and reduced the levels of ROS, H

conclusionKnockdown of TRIM8 can alleviate H/R-induced oxidative stress by triggering the PI3K/AKT pathway, thus attenuating pyropyosis and apoptosis in vitro.

Indexed as

Acute Kidney InjuryApoptosisCarrier ProteinsCells, CulturedCell SurvivalHumansHydrogen PeroxideHypoxiaNerve Tissue ProteinsOxidative StressPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPyroptosisReactive Oxygen SpeciesReperfusion InjurySignal TransductionCarrier ProteinsHydrogen PeroxideNerve Tissue ProteinsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReactive Oxygen SpeciesTRIM8 protein, humanapoptosisoxidative stresspyroptosisrenal I/R injuryTRIM8

Identifiers

PMID34916780
PMCPMC8670861
OpenAlexW4200095994

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.