Evidence map›Paper›PMID 32149133›Full record

ArticleBioMed research international2020

Identification of Three lncRNAs as Potential Predictive Biomarkers of Lung Adenocarcinoma.

Donghui Jin, Yuxuan Song, Yuan Chen, Peng Zhang

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 34 citations in OpenAlex.

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  10. Prognostic Value of Genomic Instability of mFrontiers in cell and developmental biology · 2022
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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

4 authors at 1 institution in 1 country.

Donghui JinCardiovascular Thoracic Surgery Department, Tianjin Medical University General Hospital, 154 Anshan Road, Heping District, Tianjin 300052, China.ORCID https://orcid.org/0000-0001-5109-6856
Yuxuan SongDepartment of Urology, Tianjin Medical University General Hospital, 154 Anshan Road, Heping District, Tianjin 300052, China.ORCID https://orcid.org/0000-0001-8326-0948
Yuan ChenCardiovascular Thoracic Surgery Department, Tianjin Medical University General Hospital, 154 Anshan Road, Heping District, Tianjin 300052, China.ORCID https://orcid.org/0000-0002-3579-7705
Peng ZhangCardiovascular Thoracic Surgery Department, Tianjin Medical University General Hospital, 154 Anshan Road, Heping District, Tianjin 300052, China.ORCID https://orcid.org/0000-0002-2444-0225
Tianjin Medical University General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLung cancer is the most common cancer and the most common cause of cancer-related death worldwide. However, the molecular mechanism of its development is unclear. It is imperative to identify more novel biomarkers.

methodsTwo datasets (GSE70880 and GSE113852) were downloaded from the Gene Expression Omnibus (GEO) database and used to identify the differentially expressed genes (DEGs) between lung cancer tissues and normal tissues. Then, we constructed a competing endogenous RNA (ceRNA) network and a protein-protein interaction (PPI) network and performed gene ontology (GO) analysis, Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis, and survival analyses to identify potential biomarkers that are related to the diagnosis and prognosis of lung cancer.

resultsA total of 41 lncRNAs and 805 mRNAs were differentially expressed in lung cancer. The ceRNA network contained four lncRNAs (CLDN10-AS1, SFTA1P, SRGAP3-AS2, and ADAMTS9-AS2), 21 miRNAs, and 48 mRNAs. Functional analyses revealed that the genes in the ceRNA network were mainly enriched in cell migration, transmembrane receptor, and protein kinase activity. mRNAs DLGAP5, E2F7, MCM7, RACGAP1, and RRM2 had the highest connectivity in the PPI network. Immunohistochemistry (IHC) demonstrated that mRNAs DLGAP5, MCM7, RACGAP1, and RRM2 were upregulated in lung adenocarcinoma (LUAD). Survival analyses showed that lncRNAs CLDN10-AS1, SFTA1P, and ADAMTS9-AS2 were associated with the prognosis of LUAD.

conclusionlncRNAs CLDN10-AS1, SFTA1P, and ADAMTS9-AS2 might be the biomarkers of LUAD. For the first time, we confirmed the important role of lncRNA CLDN10-AS1 in LUAD.

Indexed as

Adenocarcinoma of LungBiomarkers, TumorDatabases, FactualGene Expression Regulation, NeoplasticGene OntologyGene Regulatory NetworksGTPase-Activating ProteinsHumansLungLung NeoplasmsMinichromosome Maintenance Complex Component 7Neoplasm ProteinsPrognosisProtein Interaction MapsRibonucleoside Diphosphate ReductaseRNA, Long NoncodingBiomarkers, TumorDLGAP5 protein, humanGTPase-Activating ProteinsMCM7 protein, humanmgcRacGAPMinichromosome Maintenance Complex Component 7Neoplasm ProteinsRibonucleoside Diphosphate Reductaseribonucleotide reductase M2RNA, Long NoncodingRNA, Messenger

Identifiers

PMID32149133
PMCPMC7053454
OpenAlexW3007333736

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LicenceCC BY
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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.