Evidence map›Paper›PMID 30729033›Full record

ArticleNPJ genomic medicine2019

Integrative analysis with expanded DNA methylation data reveals common key regulators and pathways in cancers.

Shicai Fan, Jianxiong Tang, Nan Li, Ying Zhao, Rizi Ai, Kai Zhang, Mengchi Wang, Wei Du, Wei Wang

Open access · goldAbstract read
In one paragraph

Article in NPJ genomic medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Crosstalk Between Inflammatory Signaling and Methylation in Cancer.Frontiers in cell and developmental biology · 2021
    Review
  20. 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

9 authors at 3 institutions in 2 countries.

Shicai Fan1School of Automation Engineering, University of Electronic Science and Technology of China, 611731 Chengdu, Sichuan China.
Jianxiong Tang1School of Automation Engineering, University of Electronic Science and Technology of China, 611731 Chengdu, Sichuan China.
Nan Li3Department of Chemistry and Biochemistry, University of California, San Diego, CA 92093-0359 USA.
Ying Zhao3Department of Chemistry and Biochemistry, University of California, San Diego, CA 92093-0359 USA.
Rizi Ai3Department of Chemistry and Biochemistry, University of California, San Diego, CA 92093-0359 USA.
Kai Zhang3Department of Chemistry and Biochemistry, University of California, San Diego, CA 92093-0359 USA.ORCID 0000-0003-3454-7357
Mengchi Wang3Department of Chemistry and Biochemistry, University of California, San Diego, CA 92093-0359 USA.
Wei Du4Key Laboratory of Symbolic Computation and Knowledge Engineering of Ministry of Education, Jilin University, 130012 Changchun, China.
Wei Wang3Department of Chemistry and Biochemistry, University of California, San Diego, CA 92093-0359 USA.
University of San Diego · USUniversity of Electronic Science and Technology of China · CNJilin University · CN

Funding

Integrated analysis of genetic variation and epigenomic dataR01HG009626 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WANG, WEI · 2017 to 2025
$4.5M
NHGRI NIH HHS R01 HG009626
6 · The paper itself

Abstract

The integration of genomic and DNA methylation data has been demonstrated as a powerful strategy in understanding cancer mechanisms and identifying therapeutic targets. The TCGA consortium has mapped DNA methylation in thousands of cancer samples using Illumina Infinium Human Methylation 450 K BeadChip (Illumina 450 K array) that only covers about 1.5% of CpGs in the human genome. Therefore, increasing the coverage of the DNA methylome would significantly leverage the usage of the TCGA data. Here, we present a new model called EAGLING that can expand the Illumina 450 K array data 18 times to cover about 30% of the CpGs in the human genome. We applied it to analyze 13 cancers in TCGA. By integrating the expanded methylation, gene expression, and somatic mutation data, we identified the genes showing differential patterns in each of the 13 cancers. Many of the triple-evidenced genes identified in majority of the cancers are biomarkers or potential biomarkers. Pan-cancer analysis also revealed the pathways in which the triple-evidenced genes are enriched, which include well known ones as well as new ones, such as axonal guidance signaling pathway and pathways related to inflammatory processing or inflammation response. Triple-evidenced genes, particularly TNXB, RRM2, CELSR3, SLC16A3, FANCI, MMP9, MMP11, SIK1, and TRIM59 showed superior predictive power in both tumor diagnosis and prognosis. These results have demonstrated that the integrative analysis using the expanded methylation data is powerful in identifying critical genes/pathways that may serve as new therapeutic targets.

Identifiers

PMID30729033
PMCPMC6358616
OpenAlexW2905459733

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.