Evidence map›Paper›PMID 26898709›Full record

ArticleScientific reports2016

Modulation of E-cadherin expression promotes migration ability of esophageal cancer cells.

Shujun Li, Xuebo Qin, Song Chai, Changbao Qu, Xiaolu Wang, Helin Zhang

Open access · goldAbstract 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
1.5field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Viscoelasticity, Like Forces, Plays a Role in Mechanotransduction.Frontiers in cell and developmental biology · 2022
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  4. New Insights Into Cancer Chronotherapies.Frontiers in pharmacology · 2021
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  8. Updates on mechanistic insights and targeting of tumour metastasis.Journal of cellular and molecular medicine · 2020
    Review
  9. Article
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  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

6 authors at 3 institutions in 1 country.

Shujun LiDepartment of Thoracic Surgery, The Second Hospital of Hebei Medical University, Shijiazhuang, 050051, China.
Xuebo QinDepartment of Thoracic Surgery, Hebei Chest Hospital, Shijiazhuang, 050051, China.
Song ChaiCancer Center, The Second Hospital of Hebei Medical University, Shijiazhuang, 050051, China.
Changbao QuCancer Center, The Second Hospital of Hebei Medical University, Shijiazhuang, 050051, China.
Xiaolu WangCancer Center, The Second Hospital of Hebei Medical University, Shijiazhuang, 050051, China.
Helin ZhangDepartment of Thoracic Surgery, The Second Hospital of Hebei Medical University, Shijiazhuang, 050051, China.
Hebei Medical University · CNSecond Hospital of Hebei Medical University · CNHospital of Hebei Province · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Losing the E-cadherin plays an important role in the metastasis of cancer. The regulation of the expression of E-cadherin is unclear. Circadian rhythm alteration is associated with the pathogenesis of a number of cancers. This study aims to investigate the role of one of the circadian proteins, period-2 (Per2) in repressing the expression of E-cadherin in esophageal cancer (esophageal cancer). We observed that the levels of circadian protein Per2 were significantly increased and E-cadherin was significantly decreased in the tissue of human esophageal cancer with metastasis as compared with non-metastatic esophageal cancer. Overexpression of Per2 in the esophageal cancer cells markedly repressed the expression of E-cadherin. The pHDAC1 was detected in human esophageal cancer with metastasis, which was much less in the esophageal cancer tissue without metastasis. Overexpression of Per2 increased the levels of pHDAC1 as well as the E-cadherin repressors at the E-cadherin promoter locus. Overexpression of Per2 markedly increased the migratory capacity of esophageal cancer cells, which was abolished by the inhibition of HDAC1. We conclude that Per-2 plays an important role in the esophageal cancer cell metastasis, which may be a novel therapeutic target for the treatment of esophageal cancer.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedCadherinsCarcinoma, Squamous CellCell Line, TumorCell MovementCircadian RhythmEsophageal NeoplasmsFemaleGenes, ReporterHistone Deacetylase 1HumansLuciferasesLymphatic MetastasisMaleCadherinsHDAC1 protein, humanHistone Deacetylase 1LuciferasesPER2 protein, humanPeriod Circadian ProteinsRNA, Small Interfering

Identifiers

PMID26898709
PMCPMC4761978
OpenAlexW2462885196

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.