Evidence map›Paper›PMID 30880552›Full record

ArticleEpigenetics2019

Integrative analysis identifies DNMTs against immune-infiltrating neutrophils and dendritic cells in colorectal cancer.

Qili Shi, Libing Shen, Jun Gan, Lirong He, Jing Lin, Shiyu Guo, Zi Xiong, Jie Lin, Shun Zhang

Abstract read
In one paragraph

Article in Epigenetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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.

Qili Shia Stem Cell and Regenerative Medicine Laboratory , Ningbo No. 2 Hospital , Ningbo , Zhejiang , P.R. China.
Libing Shenb Institute of Neuroscience, Shanghai Institute for Biological Sciences , Chinese Academy of Sciences , Shanghai , P.R. China.
Jun Ganc School of Laboratory Medicine and Life Science , Wenzhou Medical University , Wenzhou , Zhejiang , P.R. China.
Lirong Hea Stem Cell and Regenerative Medicine Laboratory , Ningbo No. 2 Hospital , Ningbo , Zhejiang , P.R. China.
Jing Lina Stem Cell and Regenerative Medicine Laboratory , Ningbo No. 2 Hospital , Ningbo , Zhejiang , P.R. China.ORCID 0000-0002-0700-4448
Shiyu Guoa Stem Cell and Regenerative Medicine Laboratory , Ningbo No. 2 Hospital , Ningbo , Zhejiang , P.R. China.
Zi Xionga Stem Cell and Regenerative Medicine Laboratory , Ningbo No. 2 Hospital , Ningbo , Zhejiang , P.R. China.
Jie Lina Stem Cell and Regenerative Medicine Laboratory , Ningbo No. 2 Hospital , Ningbo , Zhejiang , P.R. China.ORCID 0000-0003-2364-7993
Shun Zhanga Stem Cell and Regenerative Medicine Laboratory , Ningbo No. 2 Hospital , Ningbo , Zhejiang , P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular characterizations, including microsatellite instability (MSI) and the CpG island methylator phenotype (CIMP) showed strong associations in colorectal carcinoma (CRC) and provided a deeper understanding of the etiology of disease. However, the global relationship between epigenetic alternations and changes in mRNA expression in CRC remains largely undefined, especially regarding the roles of DNA methyltransferases (DNMTs). Here, we conducted a systematic network comparison to explore the global conservation between co-expressed and co-methylated modules. We successfully identified immune-related modules that were regulated by DNMTs and had strong associations with immune-infiltrating neutrophils and dendritic cells in CRC. Moreover, we found that genes in those modules were prognostic for CRC, with 97.1% (168/173) being significantly influenced by DNMTs. Thus, this study resolved an interaction between DNA methylation and mRNA expression through DNMTs. Additionally, we provided evidence that DNMTs control the global hypomethylation of oncogenes, including ALOX5AP and CSF3R that otherwise have high methylation in normal colons. Such genes were also more sensitive to DNMT changes, such as in CRC. Collectively, our analyzes provided a systems biology approach to investigate the association among different molecular phenotypes in diseases.

Indexed as

DNA Methylation5-Lipoxygenase-Activating ProteinsBiomarkers, TumorCarcinomaColorectal NeoplasmsDendritic CellsDNA (Cytosine-5-)-MethyltransferasesEpigenesis, GeneticGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansNeutrophilsReceptors, Colony-Stimulating FactorRNA, Messenger5-Lipoxygenase-Activating ProteinsALOX5AP protein, humanBiomarkers, TumorCSF3R protein, humanDNA (Cytosine-5-)-MethyltransferasesReceptors, Colony-Stimulating FactorRNA, MessengerColorectal carcinomadendritic cellDNMTsneutrophilWGCNA

Identifiers

PMID30880552
PMCPMC6557545

What OpenQuestion holds

Textmetadata
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.