Evidence map›Paper›PMID 32860318›Full record

ArticleCancer medicine2020

Identification of a novel prognostic DNA methylation signature for lung adenocarcinoma based on consensus clustering method.

Qidong Cai, Boxue He, Hui Xie, Pengfei Zhang, Xiong Peng, Yuqian Zhang, Zhenyu Zhao, Xiang Wang

Abstract read
In one paragraph

Article in Cancer medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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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

8 authors.

Qidong CaiDepartment of Thoracic Surgery, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.ORCID 0000-0003-0311-0697
Boxue HeDepartment of Thoracic Surgery, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hui XieDepartment of Thoracic Surgery, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Pengfei ZhangDepartment of Thoracic Surgery, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Xiong PengDepartment of Thoracic Surgery, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Yuqian ZhangDepartment of Thoracic Surgery, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Zhenyu ZhaoDepartment of Thoracic Surgery, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Xiang WangDepartment of Thoracic Surgery, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.ORCID 0000-0002-5211-7206

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Abnormal DNA methylation persists throughout carcinogenesis and cancer development. Hence, gene promoter methylation may act as a prognostic tool and provide new potential therapeutic targets for patients with lung adenocarcinoma (LUAD). In this study, to explore prognostic methylation signature, data regarding DNA methylation and RNA-seq, and clinical data of patients with LUAD from the Cancer Genome Atlas database (TCGA) were downloaded. After data preprocessing, the methylation data were divided into training (N = 405) and test sets (N = 62). Then, patients in the training set were assigned to five subgroups based on their different methylation levels using the consensus clustering method. We comprehensively analyzed the survival information, methylation levels, and clinical variables, including American Joint Committee on Cancer (AJCC) stage, tumor-node-metastasis (TNM) staging, age, smoking history, and gender of these five groups. Subsequently, we identified a 16-CpG prognostic signature and constructed a prognostic model, which was verified in the test set. Further analyses showed stable prognostic performance in the stratified cohorts. In conclusion, the new predictive DNA methylation signature proposed in this study may be used as an independent biomarker to assess the overall survival of LUAD patients and provide bioinformatics information for development of targeted therapy.

Indexed as

Biomarkers, TumorDNA MethylationAdenocarcinomaAgedAged, 80 and overCluster AnalysisComputational BiologyCpG IslandsDatabases, GeneticFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansLung NeoplasmsMaleMiddle AgedBiomarkers, Tumorbiomarkerconsensus clusteringDNA methylationlung adenocarcinoma

Identifiers

PMID32860318
PMCPMC7571836

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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.