Evidence map›Paper›PMID 33791386›Full record

ArticleBioMed research international2021

Identifying Novel Cell Glycolysis-Related Gene Signature Predictive of Overall Survival in Gastric Cancer.

Xin Zhao, Jiaxuan Zou, Ziwei Wang, Ge Li, Yi Lei

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. NF-BioMed research international · 2022
    Article
  6. Transcriptomic and Metabolomic Profiling inFrontiers in cell and developmental biology · 2021
    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

5 authors at 3 institutions in 1 country.

Xin ZhaoDepartment of Urology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan 646000, China.ORCID https://orcid.org/0000-0002-1768-7780
Jiaxuan ZouFuzhou Medical College of Nanchang University, Fuzhou, Jiangxi Province 344100, China.
Ziwei WangCollege of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
Ge LiDepartment of Urology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan 646000, China.ORCID https://orcid.org/0000-0001-6296-070X
Yi LeiSichuan Clinical Research Center for Nephropathy, Luzhou, Sichuan 646000, China.ORCID https://orcid.org/0000-0002-0857-6317
Affiliated Hospital of Southwest Medical University · CNNanchang University · CNUniversity of Chinese Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGastric cancer (GC) is believed to be one of the most common digestive tract malignant tumors. The prognosis of GC remains poor due to its high malignancy, high incidence of metastasis and relapse, and lack of effective treatment. The constant progress in bioinformatics and molecular biology techniques has given rise to the discovery of biomarkers with clinical value to predict the GC patients' prognosis. However, the use of a single gene biomarker can hardly achieve the satisfactory specificity and sensitivity. Therefore, it is urgent to identify novel genetic markers to forecast the prognosis of patients with GC. MATERIALS AND

methodsIn our research, data mining was applied to perform expression profile analysis of mRNAs in the 443 GC patients from The Cancer Genome Atlas (TCGA) cohort. Genes associated with the overall survival (OS) of GC were identified using univariate analysis. The prognostic predictive value of the risk factors was determined using the Kaplan-Meier survival analysis and multivariate analysis. The risk scoring system was built in TCGA dataset and validated in an independent Gene Expression Omnibus (GEO) dataset comprising 300 GC patients. Based on the median of the risk score, GC patients were grouped into high-risk and low-risk groups.

resultsWe identified four genes (

conclusionThe signature consisting of four glycolysis-related genes could be used to forecast the GC patients' prognosis.

Indexed as

Biomarkers, TumorDatabases, Nucleic AcidGene Expression Regulation, NeoplasticGlycolysisNeoplasm ProteinsStomach NeoplasmsAgedDisease-Free SurvivalFemaleHumansKaplan-Meier EstimateMaleMiddle AgedSurvival RateBiomarkers, TumorNeoplasm Proteins

Identifiers

PMID33791386
PMCPMC7982000
OpenAlexW3137171333

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.