Evidence map›Paper›PMID 34658353›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2021

[Quantitative analysis of differential proteins in liver tissues of patients with non-alcoholic steatohepatitis using iTRAQ technology].

Y Zhu, S Zhang, C Yang, W Xue, J Zhang, J Li, J Zhao, J Xu, W Huang

Open access · greenAbstract read
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. [TSPAN8 is involved in lipid metabolism in non-alcoholic fatty liver disease in mice].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2022
    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.

Y ZhuDepartment of Infectious Diseases, First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
S ZhangDepartment of Infectious Diseases, First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
C YangDepartment of Infectious Diseases, First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
W XueDepartment of Infectious Diseases, First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
J ZhangDepartment of Infectious Diseases, First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
J LiDepartment of Infectious Diseases, First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
J ZhaoDepartment of Infectious Diseases, First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
J XuDepartment of Infectious Diseases, First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
W HuangDepartment of Infectious Diseases, First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
The Affiliated Yongchuan Hospital of Chongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo screen differentially expressed proteins (DSPs) in the liver tissues of patients with nonalcoholic steatohepatitis (NASH) using proteomic technologies to identify potential therapeutic targets of NASH.

methodsLiver tissue specimens were obtained from 3 patients with pathologically confirmed NASH and 3 normal control subjects. The total proteins were extracted from the specimens, and iTRAQ reagent was used to label the peptides for liquid chromatography tandem mass spectrometry (LC-MS/MS) detection. The DSPs were identified by comparing the data against UniProt protein database using Mascot2.3.02 software and were annotated and enriched using GO database; KEGG database was used for enrichment of the pathways involving these proteins. Real-time fluorescent quantitative PCR (qPCR) was performed to detect the mRNA expressions of the significant DSPs in NASH.

resultsBy the criteria that a DSP has >1.2 or < 0.8 fold difference between NASH group and the control group and with

conclusionWe identified 648 DEPs inthe liver tissue of patients NASH using iTRAQ technology and bioinformatics methods, and among them JARID2, SYN1, COL13A1, FGD5, and GSTM4 may serve as the key target proteins of NASH.

Indexed as

Non-alcoholic Fatty Liver DiseaseChromatography, LiquidHumansProteomicsTandem Mass SpectrometryTechnologybioinformaticsdifferential proteinnon-alcoholic fatty liverproteomics

Identifiers

PMID34658353
PMCPMC8526326
OpenAlexW3206113707

What OpenQuestion holds

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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.