Evidence map›Paper›PMID 25774687›Full record

ArticlePloS one2015

The identification of specific methylation patterns across different cancers.

Chunlong Zhang, Hongyan Zhao, Jie Li, Hongbo Liu, Fang Wang, Yanjun Wei, Jianzhong Su, Dongwei Zhang, Tiefu Liu, Yan Zhang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

39 citing papers in PubMed, 58 citations in OpenAlex.

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  8. NAR cancer · 2023
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  9. Consistent DNA Hypomethylations in Prostate Cancer.International journal of molecular sciences · 2022
    Article
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  14. Review
  15. Article
  16. Article
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  19. Article
  20. Review
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.

Chunlong ZhangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.
Hongyan ZhaoDepartment of Gastroenterology, The fourth Affiliated Hospital of Harbin Medical University, Harbin, China.
Jie LiCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.
Hongbo LiuCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.
Fang WangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.
Yanjun WeiCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.
Jianzhong SuCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.
Dongwei ZhangDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Tiefu LiuDepartment of Gastroenterology, The fourth Affiliated Hospital of Harbin Medical University, Harbin, China.
Yan ZhangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.
Harbin Medical University · CNSecond Affiliated Hospital of Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Abnormal DNA methylation is known as playing an important role in the tumorgenesis. It is helpful for distinguishing the specificity of diagnosis and therapeutic targets for cancers based on characteristics of DNA methylation patterns across cancers. High throughput DNA methylation analysis provides the possibility to comprehensively filter the epigenetics diversity across various cancers. We integrated whole-genome methylation data detected in 798 samples from seven cancers. The hierarchical clustering revealed the existence of cancer-specific methylation pattern. Then we identified 331 differentially methylated genes across these cancers, most of which (266) were specifically differential methylation in unique cancer. A DNA methylation correlation network (DMCN) was built based on the methylation correlation between these genes. It was shown the hubs in the DMCN were inclined to cancer-specific genes in seven cancers. Further survival analysis using the part of genes in the DMCN revealed high-risk group and low-risk group were distinguished by seven biomarkers (PCDHB15, WBSCR17, IGF1, GYPC, CYGB, ACTG2, and PRRT1) in breast cancer and eight biomarkers (ZBTB32, OR51B4, CCL8, TMEFF2, SALL3, GPSM1, MAGEA8, and SALL1) in colon cancer, respectively. At last, a protein-protein interaction network was introduced to verify the biological function of differentially methylated genes. It was shown that MAP3K14, PTN, ACVR1 and HCK sharing different DNA methylation and gene expression across cancers were relatively high degree distribution in PPI network. The study suggested that not only the identified cancer-specific genes provided reference for individual treatment but also the relationship across cancers could be explained by differential DNA methylation.

Indexed as

DNA MethylationEpigenesis, GeneticEpigenomicsCluster AnalysisComputational BiologyDatabases, Nucleic AcidGene Expression ProfilingGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansNeoplasmsPrognosisProtein Interaction MappingProtein Interaction Maps

Identifiers

PMID25774687
PMCPMC4361543
OpenAlexW2048338967

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.