Evidence map›Paper›PMID 32945480›Full record

ArticleOncology reports2020

miR‑30a‑5p inhibits hypoxia/reoxygenation‑induced oxidative stress and apoptosis in HK‑2 renal tubular epithelial cells by targeting glutamate dehydrogenase 1 (GLUD1).

Yangbiao He, Xujun Lang, Dong Cheng, Ting Zhang, Zhihao Yang, Rongbing Xiong

Open access · hybridAbstract read
In one paragraph

Article in Oncology reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 31% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Metabolic changes in kidney stone disease.Frontiers in immunology · 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

6 authors.

Yangbiao HeDepartment of Nephrology, Jinhua Hospital of Traditional Chinese Medicine, Jinhua, Zhejiang 321017, P.R. China.
Xujun LangDepartment of Nephrology, Jinhua Hospital of Traditional Chinese Medicine, Jinhua, Zhejiang 321017, P.R. China.
Dong ChengDepartment of Nephrology, Jinhua Hospital of Traditional Chinese Medicine, Jinhua, Zhejiang 321017, P.R. China.
Ting ZhangDepartment of Nephrology, Jinhua Hospital of Traditional Chinese Medicine, Jinhua, Zhejiang 321017, P.R. China.
Zhihao YangDepartment of Nephrology, Jinhua Hospital of Traditional Chinese Medicine, Jinhua, Zhejiang 321017, P.R. China.
Rongbing XiongDepartment of Nephrology, Jinhua Hospital of Traditional Chinese Medicine, Jinhua, Zhejiang 321017, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) are reported to be involved in renal hypoxia/reoxygenation (H/R) damage. To investigate this further, human kidney (HK‑2) cells were cultured, subjected to H/R and the function of miR‑30a‑5p and glutamate dehydrogenase 1 (GLUD1) was evaluated. The results showed that, miR‑30‑5p was downregulated and GLUD1 was upregulated in HK‑2 cells exposed to H/R. The relationship between miR‑30a‑5p and GLUD1 was determined using dual luciferase assays. Primary HK‑2 cells were cultured in H/R and transfected with negative control 1 (NC1), negative control 2 (NC2), mimic, inhibitor or GLUD1 siRNA plasmids. Reactive oxygen species (ROS) generation, superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx) activities, and the rate of apoptosis in HK‑2 cells were assessed. The results showed that, miR‑30a‑5p mimic reduced the production of ROS in HK‑2 cells treated with H/R, but increased the activity of SOD, CAT and GPx. In addition, miR‑30a‑5p mimic significantly decreased H/R‑mediated apoptosis, decreased the expression of bax and activity of caspase‑3 and enhanced the expression of bcl‑2. However, miR‑30a‑5p inhibitor showed the opposite effect with regard to the degree of oxidative damage and apoptosis in H/R‑induced HK‑2 cells. Silencing GLUD1 rescued the influence of miR‑30a‑5p inhibitor on oxidative injury and apoptosis in HK‑2 cells stimulated with H/R. These results demonstrated that under H/R conditions, miR‑30a‑5p can reduce oxidative stress in vitro by targeting GLUD1, which may be a novel therapeutic target for liver failure and worth further study.

Indexed as

ApoptosisCaspase 3Cell HypoxiaCell ProliferationEpithelial CellsGene Expression Regulation, NeoplasticGlutamate DehydrogenaseHumansKidneyKidney DiseasesKidney TubulesLiver DiseasesMicroRNAsOxidative StressProto-Oncogene Proteins c-bcl-2Reactive Oxygen SpeciesBCL2 protein, humanCaspase 3GLUD1 protein, humanGlutamate DehydrogenaseMicroRNAsMIRN30b microRNA, humanProto-Oncogene Proteins c-bcl-2Reactive Oxygen Speciesapoptosisglutamate dehydrogenase 1human kidney cellshypoxia/reoxygenationmiRNA-30a-5poxidative stress

Identifiers

PMID32945480
PMCPMC7448462
OpenAlexW3048003169

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.