Evidence map›Paper›PMID 32444534›Full record

ArticleCancer biomarkers : section A of Disease markers2020

Four genes relevant to pathological grade and prognosis in ovarian cancer.

Xue Pan, Ying Chen, Song Gao

Abstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

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  16. Targeting of CD163International journal of molecular sciences · 2020
    Review
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4 · The record

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5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Xue PanDepartment of Gynecological Tumors, Shengjing Hospital of China Medical University, Shenyang, Liaoning, China.
Ying ChenDepartment of Ultrasound, Jiangnan Hospital Affiliated to Zhejiang University of Traditional Chinese Medicine, Hangzhou, Zhejiang, China.
Song GaoDepartment of Gynecological Tumors, Shengjing Hospital of China Medical University, Shenyang, Liaoning, China.
China Medical University · CNZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOvarian cancer is the common tumor in female, the prognostic of which is influenced by a series of factors. In this study, 4 genes relevant to pathological grade in ovarian cancer were screened out by the construction of weighted gene co-expression network analysis.

methodsGSE9891 with 298 ovarian cancer cases had been used to construct co-expression networks. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analyses was used to analyze the possible mechanism of genes involved in the malignant process of ovarian cancer. Hub genes were validated in other independent datasets, such as GSE63885, GSE26193 and GSE30161. Survival analysis based on the hub genes was performed by website of Kaplan Meier-plotter.

resultsThe result based on weighted gene co-expression network analysis indicated that turquoise module has the highest association with pathological grade. Gene Ontology enrichment analysis revealed that the genes in turquoise module main enrichment in inflammatory response and immune response. Kyoto Encyclopedia of Genes and Genomes enrichment analysis revealed that the genes in turquoise module main enrichment in cytokine-cytokine receptor interaction and chemokine signaling pathway. In turquoise module, a total of 4 hub genes (MS4A4A, CD163, CPR65, MS4A6A) were identified. Then, 4 hub genes were effectively verified in the test datasets (GSE63885, GSE26193 and GSE30161) and tissue samples from Shengjing Hospital of China Medical University. Survival analysis indicated that the 4 hub genes were associated with poor progression-free survival of ovarian cancer.

conclusionsIn conclusion, 4 hub genes (MS4A4A, CD163, CPR65, MS4A6A) were verified associated with pathological grade of ovarian cancer. Moreover, MS4A4A, CD163, MS4A6A may serve as a surface marker for M2 macrophages. Targeting the 4 hub genes may can improve the prognosis of ovarian cancer.

Indexed as

Gene Regulatory NetworksAntigens, CDAntigens, Differentiation, MyelomonocyticBiomarkers, TumorCarcinoma, Ovarian EpithelialCD163 AntigenCytokinesDatasets as TopicFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimateMacrophagesMembrane ProteinsNeoplasm GradingAntigens, CDAntigens, Differentiation, MyelomonocyticBiomarkers, TumorCD163 AntigenCytokinesGPR65 protein, humanMembrane ProteinsMS4A4A protein, humanMS4A6A protein, humanReceptors, Cell SurfaceReceptors, G-Protein-CoupledM2 macrophagesOvarian cancerpathological gradeprognosisWGCNA

Identifiers

PMID32444534
PMCPMC12662536
OpenAlexW3026651149

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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.