Evidence map›Paper›PMID 31558162›Full record

ArticleJournal of translational medicine2019

Methylation and transcriptome analysis reveal lung adenocarcinoma-specific diagnostic biomarkers.

Rui Li, Yi-E Yang, Yun-Hong Yin, Meng-Yu Zhang, Hao Li, Yi-Qing Qu

Abstract read
In one paragraph

Article in Journal of translational medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

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49citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

49 citing papers in PubMed.

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  17. A prognostic model based on the COL1A1-network in gastric cancer.American journal of translational research · 2023
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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Rui LiDepartment of Respiratory and Critical Care Medicine, Qilu Hospital of Shandong University, Jinan, 250012, China.
Yi-E YangDepartment of Clinical Laboratory, Qianfoshan Hospital of Shandong Province, Jinan, 250014, China.
Yun-Hong YinDepartment of Respiratory and Critical Care Medicine, Qilu Hospital of Shandong University, Jinan, 250012, China.
Meng-Yu ZhangDepartment of Respiratory and Critical Care Medicine, Qilu Hospital of Shandong University, Jinan, 250012, China.
Hao LiDepartment of Respiratory and Critical Care Medicine, Qilu Hospital of Shandong University, Jinan, 250012, China. doctorlihao@163.com.
Yi-Qing QuDepartment of Respiratory and Critical Care Medicine, Qilu Hospital of Shandong University, Jinan, 250012, China. quyiqing@sdu.edu.cn.ORCID 0000-0002-9538-7601

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDNA methylation can regulate the role of long noncoding RNAs (lncRNAs) in the development of lung adenocarcinoma (LUAD). The present study aimed to identify methylation-driven lncRNAs and mRNAs as biomarkers in the prognosis of LUAD using bioinformatics analysis.

methodsDifferentially expressed RNAs were obtained using the edge R package from 535 LUAD tissues and 59 adjacent non-LUAD tissues. Differentially methylated genes were obtained using the limma R package from 475 LUAD tissues and 32 adjacent non-LUAD tissues. Methylation-driven mRNA and lncRNA were obtained using the MethylMix R package from 465 LUAD tissues with matched DNA methylation and RNA expression and 32 non-LUAD tissues with DNA methylation. Gene ontology and ConsensusPathDB pathway analysis were performed to identify functional enrichment of methylation-driven mRNAs. Univariate and multivariate Cox regression analyses were performed to identify the independent effect of each variable for predicting the prognosis of LUAD. Kaplan-Meier curve analysis of DNA methylation and gene expression might provide potential prognostic biomarkers for LUAD patients.

resultsA total of 99 methylation-driven mRNAs and 17 methylation-driven lncRNAs were obtained. Univariate and multivariate Cox regression analysis showed that 6 lncRNAs (FOXE1, HOXB13-AS1_2, VMO1, HIST1H3F, AJ003147.8, ASXL3) were retrieved to construct a predictive model associated with overall survival in LUAD patients. Combined DNA methylation and gene expression survival analysis revealed that 4 lncRNAs (AC023824.1, AF186192.1, LINC01354 and WASIR2) and 8 mRNAs (S1PR1, CCDC181, F2RL1, EFS, KLHDC9, MPV17L, GKN2, ITPRIPL1) might act as independent biomarkers for the prognosis of LUAD.

conclusionsMethylation-driven lncRNA and mRNA contribute to the survival of LUAD, and 4 lncRNAs and 8 mRNAs might be potential biomarkers for the prognosis of LUAD.

Indexed as

Gene Expression ProfilingAdenocarcinoma of LungBiomarkers, TumorDNA MethylationGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimateLung NeoplasmsPrognosisRisk FactorsRNA, Long NoncodingRNA, MessengerROC CurveBiomarkers, TumorRNA, Long NoncodingRNA, MessengerBiomarkersLung adenocarcinomaMethylation-driven lncRNAMethylation-driven mRNAOverall survival rate

Identifiers

PMID31558162
PMCPMC6764142

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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.