Evidence map›Paper›PMID 25050929›Full record

ArticlePloS one2014

Identification of a DNA methylome profile of esophageal squamous cell carcinoma and potential plasma epigenetic biomarkers for early diagnosis.

Xufeng Li, Fuyou Zhou, Chunyu Jiang, Yinuo Wang, Yanqiang Lu, Fei Yang, Nengchao Wang, Haijun Yang, Yanfang Zheng, Jiren Zhang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
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  13. Methylated DNA Markers of Esophageal Squamous Cancer and Dysplasia: An International Study.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020
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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

10 authors at 2 institutions in 1 country.

Xufeng LiOncology Center, ZhuJiang Hospital of Southern Medical University, Guangzhou, China.
Fuyou ZhouAnyang Cancer Hospital, Anyang, China.
Chunyu JiangOncology Center, ZhuJiang Hospital of Southern Medical University, Guangzhou, China.
Yinuo WangInstitute of Targeted Molecular Medicine, Shanghai, China.
Yanqiang LuInstitute of Targeted Molecular Medicine, Shanghai, China.
Fei YangInstitute of Targeted Molecular Medicine, Shanghai, China.
Nengchao WangAnyang Cancer Hospital, Anyang, China.
Haijun YangAnyang Cancer Hospital, Anyang, China.
Yanfang ZhengOncology Center, ZhuJiang Hospital of Southern Medical University, Guangzhou, China.
Jiren ZhangOncology Center, ZhuJiang Hospital of Southern Medical University, Guangzhou, China; Institute of Targeted Molecular Medicine, Shanghai, China.
Southern Medical University · CNAnyang Tumor Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA methylation is a critical epigenetic mechanism involved in key cellular processes. Its deregulation has been linked to many human cancers including esophageal squamous cell carcinoma (ESCC). This study was designed to explore the whole methylation status of ESCC and to identify potential plasma biomarkers for early diagnosis. We used Infinium Methylation 450k array to analyze ESCC tissues (n = 4), paired normal surrounding tissues (n = 4) and normal mucosa from healthy individuals (n = 4), and combined these with gene expression data from the GEO database. One hundred and sixty eight genes had differentially methylated CpG sites in their promoter region and a gene expression pattern inverse to the direction of change in DNA methylation. These genes were involved in several cancer-related pathways. Three genes were validated in additional 42 ESCC tissues and paired normal surrounding tissues. The methylation frequency of EPB41L3, GPX3, and COL14A1 were higher in tumor tissues than in normal surrounding tissues (P < 0.017). The higher methylation frequency of EPB41l3 was correlated with large tumor size (P = 0.044) and advanced pT tumor stage (P = 0.001). The higher methylation frequency of GPX3 and COL14A1 were correlated with advanced pN tumor stage (P = 0.001 and P < 0.001). The methylation of EPB41L3, GPX3, and COL14A1 genes were only found in ESCC patients' plasma, but not in normal individuals upon testing 42 ESCC patients and 50 healthy individuals. Diagnostic sensitivity was increased when methylation of any of the 3 genes were counted (64.3% sensitivity and 100% specificity). These differentially methylated genes in plasma may be used as biomarkers for early diagnosis of ESCC.

Indexed as

DNA MethylationGene Expression Regulation, NeoplasticAgedCarcinoma, Squamous CellCollagenCpG IslandsEarly DiagnosisEpigenesis, GeneticEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaEsophagusFemaleGlutathione PeroxidaseGlycoproteinsHumansMaleCOL14A1 protein, humanCollagenEPB41L3 protein, humanGlutathione PeroxidaseGlycoproteinsGPX3 protein, humanMicrofilament Proteins

Identifiers

PMID25050929
PMCPMC4106874
OpenAlexW2014493707

What OpenQuestion holds

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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.