Evidence map›Paper›PMID 27546520›Full record

ArticleScientific reports2016

Filtrating colorectal cancer associated genes by integrated analyses of global DNA methylation and hydroxymethylation in cancer and normal tissue.

Ming Li, Fei Gao, Yudong Xia, Yi Tang, Wei Zhao, Congcong Jin, Huijuan Luo, Junwen Wang, Qingshu Li, Yalan Wang

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
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  3. Article
  4. Review
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  7. Article
  8. Review
  9. Article
  10. Article
  11. DNA methylation profiles in cancer diagnosis and therapeutics.Clinical and experimental medicine · 2018
    Review
  12. The role ofOncotarget · 2017
    Article
  13. Article
  14. 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

10 authors.

Ming LiDepartment of Pathology, Molecular Medicine and Cancer Research Center, Chongqing Medical University, 1 Yixueyuan Road, Yuzhong District, Chongqing 400016, China.
Fei GaoBGI-Shenzhen, Build 11, Beishan Industrial Zone, Yantian District, Shenzhen 518083, China.
Yudong XiaBGI-Shenzhen, Build 11, Beishan Industrial Zone, Yantian District, Shenzhen 518083, China.
Yi TangDepartment of Pathology, Molecular Medicine and Cancer Research Center, Chongqing Medical University, 1 Yixueyuan Road, Yuzhong District, Chongqing 400016, China.
Wei ZhaoDepartment of Pathology, Molecular Medicine and Cancer Research Center, Chongqing Medical University, 1 Yixueyuan Road, Yuzhong District, Chongqing 400016, China.
Congcong JinDepartment of Pathology, Molecular Medicine and Cancer Research Center, Chongqing Medical University, 1 Yixueyuan Road, Yuzhong District, Chongqing 400016, China.
Huijuan LuoBGI-Shenzhen, Build 11, Beishan Industrial Zone, Yantian District, Shenzhen 518083, China.
Junwen WangBGI-Shenzhen, Build 11, Beishan Industrial Zone, Yantian District, Shenzhen 518083, China.
Qingshu LiDepartment of Pathology, Molecular Medicine and Cancer Research Center, Chongqing Medical University, 1 Yixueyuan Road, Yuzhong District, Chongqing 400016, China.
Yalan WangDepartment of Pathology, Molecular Medicine and Cancer Research Center, Chongqing Medical University, 1 Yixueyuan Road, Yuzhong District, Chongqing 400016, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, 5-hydroxymethylcytosine patterning across the tumor genome was considered as a hallmark of cancer development and progression. However, locus-specific difference of hydroxymethylation between colorectal cancer and normal tissue is unknown. In this study, we performed a newly developed method, HMST-seq, to profile 726 aberrant methylated loci and 689 aberrant hydroxymethylated loci synchronously in genome wide of colorectal cancers, majority of which presented higher methylation or lower hydroxymethylationin than in normal group. Besides, abnormal hydroxymethylated modification was more frequently occur at proximal regions close to TSSs and TSSs regions than abnormal methylation. Subsequently, we screened four genes (ALOX15, GHRHR, TFPI2 and TKTL1) with aberrant methylation and aberrant hydroxymethylation at some genome position by functional enrichment analysis as candidate genes associated with colorectal cancer. Our results may allow us to select differentially epigenetically modified target genes implicated in colorectal cancer tumorigenesis.

Indexed as

DNA MethylationGene Regulatory Networks5-MethylcytosineArachidonate 15-LipoxygenaseColorectal NeoplasmsEpigenesis, GeneticGene Expression Regulation, NeoplasticGlycoproteinsHumansSequence Analysis, DNATransketolase5-hydroxymethylcytosine5-MethylcytosineALOX15 protein, humanArachidonate 15-LipoxygenaseGlycoproteinstissue-factor-pathway inhibitor 2TKTL1 protein, humanTransketolase

Identifiers

PMID27546520
PMCPMC4992821

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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.