Evidence map›Paper›PMID 35342299›Full record

ArticleInternational journal of general medicine2022

Screening of Potential Key Biomarkers for Ewing Sarcoma: Evidence from Gene Array Analysis.

Duming Zhong, Dan Chen, Guangquan Zhang, Shaobai Lin, Runhong Mei, Xuefeng Yu

Open access · goldAbstract read
In one paragraph

Article in International journal of general medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 54% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 1 institution in 1 country.

Duming ZhongDepartment of Orthopedics, The Fourth Affiliated Hospital of Nanchang University, Nanchang, People's Republic of China.ORCID 0000-0001-5313-7308
Dan ChenDepartment of Orthopedics, The Fourth Affiliated Hospital of Nanchang University, Nanchang, People's Republic of China.
Guangquan ZhangDepartment of Orthopedics, The Fourth Affiliated Hospital of Nanchang University, Nanchang, People's Republic of China.
Shaobai LinDepartment of Orthopedics, The Fourth Affiliated Hospital of Nanchang University, Nanchang, People's Republic of China.ORCID 0000-0003-1134-5912
Runhong MeiDepartment of Orthopedics, The Fourth Affiliated Hospital of Nanchang University, Nanchang, People's Republic of China.ORCID 0000-0002-5163-3559
Xuefeng YuDepartment of Orthopedics, The Fourth Affiliated Hospital of Nanchang University, Nanchang, People's Republic of China.ORCID 0000-0003-2520-5881
Nanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Ewing's sarcoma (ES) is a common bone cancer in children and adolescents. There are ethnic differences in the incidence and treatment effects. People have made great efforts to clarify the cause; however, the molecular mechanism of ES is still poorly understood. Methods: We download the microarray datasets GSE68776, GSE45544 and GSE17674 from the Gene Expression Omnibus (GEO) database. The differentially expressed genes (DEGs) of the three datasets were screened and enrichment analysis was performed. STRING and Cytoscape were used to carry out module analysis, building a protein-protein interaction (PPI) network. Finally, a series of analyses such as survival analysis and immune infiltration analysis were performed on the selected genes. Results: A total of 629 differentially expressed genes were screened, including 206 up-regulated genes and 423 down-regulated genes. The pathways and rich-functions of DEGs include protein activation cascade, carbohydrate binding, cell-cell adhesion junctions, mitotic cell cycle, p53 pathway, and cancer pathways. Then, a total of 10 hub genes were screened out. Biological process analysis showed that these genes were mainly enriched in mitotic nuclear division, protein kinase activity, cell division, cell cycle, and protein phosphorylation. Conclusion: Survival analysis and multiple gene comparison analysis showed that CDCA8, MAD2L1 and FANCI may be involved in the occurrence and prognosis of ES. The purpose of our study is to clarify the DEG and key genes, which will help us know more about the molecular mechanisms of ES, provide potential pathway or targets for the diagnosis and treatment.

Indexed as

biomarkersdifferentially expressed genesEwing sarcomamicroarrayprotein interaction

Identifiers

PMID35342299
PMCPMC8943648
OpenAlexW4220932695

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.