Evidence map›Paper›PMID 32716025›Full record

ArticleBioscience reports2020

Construction of a novel prognostic-predicting model correlated to ovarian cancer.

Weichun Tang, Jie Li, Xinxia Chang, Lizhou Jia, Qi Tang, Ying Wang, Yanli Zheng, Lizhou Sun, Zhenqing Feng

Abstract read
In one paragraph

Article in Bioscience reports, 2020. 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
–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

6 citing papers in PubMed.

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  6. Clinical Significance and Potential Role ofFrontiers in genetics · 2021
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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

9 authors.

Weichun Tang *National Health Commission Key Laboratory of Antibody Technique, Nanjing Medical University, Nanjing, People's Republic of China.
Jie Li *Department of Nursing, The Second Affiliated Hospital of Nantong University, Nantong, People's Republic of China.
Xinxia ChangNational Health Commission Key Laboratory of Antibody Technique, Nanjing Medical University, Nanjing, People's Republic of China.
Lizhou JiaNational Health Commission Key Laboratory of Antibody Technique, Nanjing Medical University, Nanjing, People's Republic of China.
Qi TangNational Health Commission Key Laboratory of Antibody Technique, Nanjing Medical University, Nanjing, People's Republic of China.
Ying WangDepartment of Gynaecology and Obstetrics, The Second Affiliated Hospital of Nantong University, Nantong, People's Republic of China.
Yanli ZhengDepartment of Gynaecology and Obstetrics, The Second Affiliated Hospital of Nantong University, Nantong, People's Republic of China.
Lizhou SunDepartment of Obstetrics and Gynecology, First Affiliated Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
Zhenqing FengNational Health Commission Key Laboratory of Antibody Technique, Nanjing Medical University, Nanjing, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOvarian cancer (OC) is one of the most lethal gynecological cancers worldwide. The pathogenesis of the disease and outcomes prediction of OC patients remain largely unclear. The present study aimed to explore the key genes and biological pathways in ovarian carcinoma development, as well as construct a prognostic model to predict patients' overall survival (OS).

resultsWe identified 164 up-regulated and 80 down-regulated differentially expressed genes (DEGs) associated with OC. Gene Ontology (GO) term enrichment showed DEGs mainly correlated with spindle microtubes. For Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways, cell cycle was mostly enriched for the DEGs. The protein-protein interaction (PPI) network yielded 238 nodes and 1284 edges. Top three modules and ten hub genes were further filtered and analyzed. Three candidiate drugs targeting for therapy were also selected. Thirteen OS-related genes were selected and an eight-mRNA model was present to stratify patients into high- and low-risk groups with significantly different survival.

conclusionsThe identified DEGs and biological pathways may provide new perspective on the pathogenesis and treatments of OC. The identified eight-mRNA signature has significant clinical implication for outcome prediction and tailored therapy guidance for OC patients.

Indexed as

Gene Expression ProfilingTranscriptomeAntineoplastic AgentsBiomarkers, TumorCase-Control StudiesClinical Decision-MakingDatabases, GeneticFemaleGene Regulatory NetworksHumansMolecular Targeted TherapyOvarian NeoplasmsPrecision MedicinePredictive Value of TestsPrognosisProtein Interaction MapsAntineoplastic AgentsBiomarkers, Tumorbioinformaticsbiological functionhub genesOvarian cancerprognostic model

Identifiers

PMID32716025
PMCPMC7414523

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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.