Evidence map›Paper›PMID 30405856›Full record

ArticleDisease markers2018

Identification of Core Biomarkers Associated with Outcome in Glioma: Evidence from Bioinformatics Analysis.

Rong-Xin Geng, Ning Li, Yang Xu, Jun-Hui Liu, Fan-En Yuan, Qian Sun, Bao-Hui Liu, Qian-Xue Chen

Abstract read
In one paragraph

Article in Disease markers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

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  9. Frontiers in oncology · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. Bioinformatics-Based Study to Investigate Potential Differentially Expressed Genes and miRNAs in Pediatric Sepsis.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  14. Article
  15. Article
  16. Article
  17. Article
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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

8 authors.

Rong-Xin GengDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.ORCID 0000-0002-9442-7202
Ning LiDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan, China.ORCID 0000-0003-3175-8343
Yang XuDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.ORCID 0000-0002-0340-1163
Jun-Hui LiuDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Fan-En YuanDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.ORCID 0000-0002-3344-6805
Qian SunDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.ORCID 0000-0003-3659-3242
Bao-Hui LiuDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.ORCID 0000-0001-5821-6945
Qian-Xue ChenDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.ORCID 0000-0002-9413-1030

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioma is the most common neoplasm of the central nervous system (CNS); the progression and outcomes of which are affected by a complicated network of genes and pathways. We chose a gene expression profile of GSE66354 from GEO database to search core biomarkers during the occurrence and development of glioma. A total of 149 samples, involving 136 glioma and 13 normal brain tissues, were enrolled in this article. 1980 differentially expressed genes (DEGs) including 697 upregulated genes and 1283 downregulated genes between glioma patients and healthy individuals were selected using GeoDiver and GEO2R tool. Then, gene ontology (GO) analysis as well as Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis were carried out using the Database for Annotation, Visualization and Integrated Discovery (DAVID). Moreover, Cytoscape with Search Tool for the Retrieval of Interacting Genes (STRING) and Molecular Complex Detection (MCODE) plug-in was employed to imagine protein-protein interaction (PPI) of these DEGs. The upregulated genes were enriched in cell cycle, ECM-receptor interaction, and p53 signaling pathway, while the downregulated genes were enriched in retrograde endocannabinoid signaling, glutamatergic synapse, morphine addiction, GABAergic synapse, and calcium signaling pathway. Subsequently, 4 typical modules were discovered by the PPI network utilizing MCODE software. Besides, 15 hub genes were chosen according to the degree of connectivity, including TP53, CDK1, CCNB1, and CCNB2, the Kaplan-Meier analysis of which was further identified. In conclusion, this bioinformatics analysis indicated that DEGs and core genes, such as TP53, might influence the development of glioma, especially in tumor proliferation, which were expected to be promising biomarkers for diagnosis and treatment of glioma.

Indexed as

Biomarkers, TumorBrainBrain NeoplasmsGene Expression ProfilingGene Expression Regulation, NeoplasticGliomaHumansTranscriptomeBiomarkers, Tumor

Identifiers

PMID30405856
PMCPMC6199874

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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.