Evidence map›Paper›PMID 28748258›Full record

ArticleJournal of cancer research and clinical oncology2017

EZH2 is involved in silencing of WNT5A during epithelial-mesenchymal transition of colon cancer cell line.

Jianxin Tao, Liping Shi, Longchang Huang, Haoze Shi, Hang Chen, Yixin Wang, Tong Wang

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2017. 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
0.9field-weighted citation impact, top 26% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  5. Review
  6. Article
  7. Review
  8. WNT5B in Physiology and Disease.Frontiers in cell and developmental biology · 2021
    Review
  9. Review
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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

7 authors at 1 institution in 1 country.

Jianxin TaoDepartment of Endoscopy Surgery, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, 214023, People's Republic of China.
Liping ShiDepartment of Endoscopy Surgery, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, 214023, People's Republic of China.
Longchang HuangDepartment of Endoscopy Surgery, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, 214023, People's Republic of China.
Haoze ShiDepartment of Endoscopy Surgery, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, 214023, People's Republic of China.
Hang ChenDepartment of Endoscopy Surgery, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, 214023, People's Republic of China.
Yixin WangDepartment of Endoscopy Surgery, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, 214023, People's Republic of China.
Tong WangDepartment of Endoscopy Surgery, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, 214023, People's Republic of China. aanti@163.com.ORCID http://orcid.org/0000-0002-2111-7086
Wuxi People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTransforming growth factor-β (TGF-β) induction of epithelial-mesenchymal transition (EMT) in SW480 was established as a system for studies of colon cancer metastasis. However, the epigenetic mechanisms underlying this process remain unknown. In mammal, polycomb repressive complex-2 (PRC2) is a highly conserved histone methyltransferase involved in epigenetic regulations. Enhancer of zeste Homolog 2 (EZH2) is the catalytic subunit of PRC2, which catalyzes methylation of lysine 27 of histone H3 (H3K27).

methodsAn inducible EMT system in colorectal cancer was utilized to study its mechanistic and phenotypic changes. Particularly, gene expression analysis was studied after immunoprecipitation.

resultsIn this study, we reported that EZH2 is significantly enriched in the promoter region of WNT5A after TGF-β induction in SW480 colon cancer cell line, which in turn silenced the expression of WNT5A. Furthermore, EZH2 inhibitor antagonized the TGF-β-induced morphological conversion associated with epithelial-mesenchymal transition (EMT). Conversely, inhibition of histone H3K27me3 reader CBX does not affect the WNT5A expression level during TGF-β-induced EMT.

conclusionsOur results indicate that EZH2 was essential for the silencing of WNT5A during TGF-β-induced epithelial-mesenchymal transition of colon cancer cells.

Indexed as

Epithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticApoptosisCell ProliferationColonic NeoplasmsDNA MethylationEnhancer of Zeste Homolog 2 ProteinEpigenesis, GeneticHistonesHumansMicroRNAsPromoter Regions, GeneticTransforming Growth Factor betaTumor Cells, CulturedWnt-5a ProteinEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanHistonesMicroRNAsTransforming Growth Factor betaWnt-5a ProteinWNT5A protein, humanEnhancer of zeste Homolog 2Epithelial to mesenchymal transitionHistone 3 lysine 27 trimethylationTransforming growth factor-βWNT signaling

Identifiers

PMID28748258
PMCPMC11819127
OpenAlexW2737985553

What OpenQuestion holds

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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.