Evidence map›Paper›PMID 31181055›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2019

Differentially Expressed Gene Screening, Biological Function Enrichment, and Correlation with Prognosis in Non-Small Cell Lung Cancer.

He Huang, Qingdong Huang, Tingyu Tang, Xiaoxi Zhou, Liang Gu, Xiaoling Lu, Fang Liu

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

He HuangDepartment of Respiratory, Zhejiang Hospital, Hangzhou, Zhejiang, China (mainland).
Qingdong HuangDepartment of Respiratory, Zhejiang Hospital, Hangzhou, Zhejiang, China (mainland).
Tingyu TangDepartment of Respiratory, Zhejiang Hospital, Hangzhou, Zhejiang, China (mainland).
Xiaoxi ZhouDepartment of Respiratory, Zhejiang Hospital, Hangzhou, Zhejiang, China (mainland).
Liang GuDepartment of Respiratory, Zhejiang Hospital, Hangzhou, Zhejiang, China (mainland).
Xiaoling LuDepartment of Respiratory, Zhejiang Hospital, Hangzhou, Zhejiang, China (mainland).
Fang LiuDepartment of Respiratory, Zhejiang Hospital, Hangzhou, Zhejiang, China (mainland).
Zhejiang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND The aim of this study was to explore the differently expressed genes and pathways in non-small cell lung cancer (NSCLC) and their correlation with the prognosis. MATERIAL AND METHODS Gene expression data series of GSE19804, GSE101929, and GSE33532 were downloaded from the Gene Expression Ominibus (GEO) database. The overlaping differently expressed genes (DEGs) were identified form the above 3 data series. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEEG) were used to analyze the biological functions and signal pathways of DEGs. The protein-protein interaction (PPI) was analyzed thorough Search Tool for the Retrieval of Interacting Gens (STRING). The relationship between the expression of hub genes and the prognosis of patients was analyzed by Kaplan-Meier Plotter online software. RESULTS Twenty-nine DEGs were identified, with 22 upregulated genes and 7 downregulated genes. The enriched biological processes were mainly related to diet-induced thermogenesis and actin filament binding. The KEGG pathways were enriched in calcium signaling, regulation of lipolysis in adipocytes, and PPAR signaling. Two downregulated genes (MMP1 and SPP1) were identified as hub genes by Cytohubba. Twenty-two dysregulated genes were correlated with patient prognosis. CONCLUSIONS Differentially expressed genes are common in NSCLC patients and can be used as biomarkers for patient prognosis.

Indexed as

Biomarkers, TumorCarcinoma, Non-Small-Cell LungComputational BiologyDatabases, GeneticGene Expression ProfilingGene Expression Regulation, NeoplasticGene OntologyGene Regulatory NetworksGenetic Predisposition to DiseaseHumansLung NeoplasmsPrognosisProtein Interaction MappingProtein Interaction MapsSignal TransductionSoftwareBiomarkers, Tumor

Identifiers

PMID31181055
PMCPMC6582684
OpenAlexW2949214362

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.