Evidence map›Paper›PMID 36583464›Full record

ReviewPharmacology research & perspectives2023

MG53: A potential therapeutic target for kidney disease.

Ben Ke, Wen Shen, Jianling Song, Xiangdong Fang

Open access · goldAbstract readReview
In one paragraph

Review in Pharmacology research & perspectives, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 21% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. MG53: A potential therapeutic target for kidney disease.Pharmacology research & perspectives · 2023
    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

4 authors at 1 institution in 1 country.

Ben KeDepartment of Nephrology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China.ORCID 0000-0002-4813-7108
Wen ShenDepartment of Cardiovascular Medicine, The Second Affiliated Hospital to Nanchang University, Nanchang, China.
Jianling SongDepartment of Nephrology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China.
Xiangdong FangDepartment of Nephrology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China.
Nanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ensuring cell survival and tissue regeneration by maintaining cellular integrity is important to the pathophysiology of many human diseases, including kidney disease. Mitsugumin 53 (MG53) is a member of the tripartite motif-containing (TRIM) protein family that plays an essential role in repairing cell membrane injury and improving tissue regeneration. In recent years, an increasing number of studies have demonstrated that MG53 plays a renoprotective role in kidney diseases. Moreover, with the beneficial effects of the recombinant human MG53 (rhMG53) protein in the treatment of kidney diseases in different animal models, rhMG53 shows significant therapeutic potential in kidney disease. In this review, we elucidate the role of MG53 and its molecular mechanism in kidney disease to provide new approaches to the treatment of kidney disease.

Indexed as

Carrier ProteinsKidney DiseasesAnimalsCell MembraneCell SurvivalHumansWound HealingCarrier Proteinsacute kidney injuryclinical applicationkidney fibrosismembrane repairMG53

Identifiers

PMID36583464
PMCPMC9801490
OpenAlexW4313297225

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.