Evidence map›Paper›PMID 26660680›Full record

Trial reportDigestive diseases and sciences2016

Sera DNA Methylation of CDH1, DNMT3b and ESR1 Promoters as Biomarker for the Early Diagnosis of Hepatitis B Virus-Related Hepatocellular Carcinoma.

Cheng-Yun Dou, Yu-Chen Fan, Chuang-Jie Cao, Yang Yang, Kai Wang

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Digestive diseases and sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 3 pooled it
1.5field-weighted citation impact, top 17% 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

18 citing papers in PubMed, 3 syntheses or guidelines pooled it, 43 citations in OpenAlex.

  1. Pooled it
  2. Utility of Liquid Biopsy Analysis in Detection of Hepatocellular Carcinoma, Determination of Prognosis, and Disease Monitoring: A Systematic Review.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2020
    Pooled it
  3. Pooled it
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  18. Promoter methylation and expression of CDH1 and susceptibility and prognosis of eyelid squamous cell carcinoma.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
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

5 authors at 2 institutions in 1 country.

Cheng-Yun DouDepartment of Hepatology, Qilu Hospital of Shandong University, Jinan, 250012, China.
Yu-Chen FanDepartment of Hepatology, Qilu Hospital of Shandong University, Jinan, 250012, China.
Chuang-Jie CaoDepartment of Pathology, The First Affiliated Hospital of Sun Yat-san University, Guangzhou, 510080, China.
Yang YangDepartment of Hepatology, Qilu Hospital of Shandong University, Jinan, 250012, China.
Kai WangDepartment of Hepatology, Qilu Hospital of Shandong University, Jinan, 250012, China. wangdoc876@126.com.
Qilu Hospital of Shandong University · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDNA methylation mainly affects tumor suppressor genes in the development of hepatocellular carcinoma (HCC). However, sera methylation of specific genes in hepatitis B virus (HBV)-related HCC remains unknown.

aimsThe purpose of this study was to identify methylation frequencies of sera E-cadherin (CDH1), DNA methyltransferase 3b (DNMT3b) and estrogen receptor 1 (ESR1) promoter in HBV-related HCC and analyze the associated clinical significance.

methodsMethylation-specific PCR was used to determine the frequencies of DNA methylation for CDH1, DNMT3b and ESR1 genes in sera from 183 patients with HCC, 47 liver cirrhosis (LC), 126 chronic hepatitis B (CHB), and 50 normal controls (NCs).

resultsSignificantly higher frequencies of methylation of CDH1, DNMT3b and ESR1 were found in HBV-related HCC compared with LC, CHB and NCs. Nodule numbers, tumor size and the presence of liver cirrhosis were significantly associated with gene methylation status in HBV-related HCC. Moreover, HBV may have a strong and enhanced effect on the concurrent methylation of CDH1, DNMT3b and ESR1 in HBV-related HCC. More importantly, combined methylation as a biomarker displayed significantly higher diagnostic value than AFP to discriminate HCC from CHB and LC.

conclusionsAberrant sera DNA methylation of CDH1, DNMT3b and ESR1 gene promoters could be a biomarker in the early diagnosis of HBV-related HCC.

Indexed as

DNA MethylationAdultAgedalpha-FetoproteinsAntigens, CDBiomarkersCadherinsCarcinoma, HepatocellularCase-Control StudiesDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3BEarly DiagnosisEstrogen Receptor alphaFemaleHepatitis B, ChronicHumansalpha-FetoproteinsAntigens, CDBiomarkersCadherinsCDH1 protein, humanDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3BESR1 protein, humanEstrogen Receptor alphaCDH1DNMT3bESR1HBV-related HCCMethylation

Identifiers

PMID26660680
OpenAlexW2267607977

What OpenQuestion holds

Textmetadata
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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.