Evidence map›Paper›PMID 24966907›Full record

ArticleInternational journal of clinical and experimental pathology2014

Snail plays an oncogenic role in glioblastoma by promoting epithelial mesenchymal transition.

Jae Kyung Myung, Seung Ah Choi, Seung-Ki Kim, Kyu-Chang Wang, Sung-Hye Park

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

39 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
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  3. BRAT1 - a new therapeutic target for glioblastoma.Cellular and molecular life sciences : CMLS · 2025
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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

5 authors at 3 institutions in 2 countries.

Jae Kyung MyungDepartment of Pathology, College of Medicine, Seoul National University Hospital Seoul, Korea.
Seung Ah ChoiDivision of Pediatric Neurosurgery, Pediatric Clinical Neuroscience Center, Seoul National University Children's Hospital Seoul, Korea.
Seung-Ki KimDivision of Pediatric Neurosurgery, Pediatric Clinical Neuroscience Center, Seoul National University Children's Hospital Seoul, Korea.
Kyu-Chang WangDivision of Pediatric Neurosurgery, Pediatric Clinical Neuroscience Center, Seoul National University Children's Hospital Seoul, Korea.
Sung-Hye ParkDepartment of Pathology, College of Medicine, Seoul National University Hospital Seoul, Korea ; Neuroscience Institute, College of Medicine, Seoul National University Seoul, Korea.
Seoul National University Children's Hospital · KRNew Generation University College · ETSeoul National University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe factors affecting glioblastoma progression are of great clinical importance since dismal outcomes have been observed for glioblastoma patients. The Snail gene is known to coordinate the regulation of tumor progression in diverse tumors through induction of epithelial mesenchymal transition (EMT); however, its role in glioblastoma is still uncertain. Therefore, we aimed to further define its role in vitro. METHODS AND

resultsThe small interfering RNA (siRNA) technique was employed to knock down Snail expression in three glioblastoma cell lines (KNS42, U87, and U373). Specific inhibition of Snail expression increased E-cadherin expression but decreased vimentin expression in all cell lines. In addition, inhibition of the expression of Snail significantly reduced the proliferation, viability, invasion, and migration of glioblastoma cells as well as increased the number of cells in the G1 phase.

conclusionsKnockdown of Snail suppresses the proliferation, viability, migration, and invasion of cells as well as inhibits cell cycle progression by promoting EMT induction. The findings suggest that expression of this gene facilitates glioblastoma progression. Therefore, these results indicate the clinical significance of Snail for use as a potential therapeutic target for glioblastoma.

Indexed as

Epithelial-Mesenchymal TransitionAntigens, CDBrain NeoplasmsCadherinsCell CycleCell Line, TumorCell MovementCell ProliferationCell SurvivalDisease ProgressionGene Expression Regulation, NeoplasticHumansNeoplasm InvasivenessOncogenesRNA InterferenceRNA, MessengerAntigens, CDCadherinsCDH1 protein, humanRNA, MessengerSnail Family Transcription FactorsTranscription FactorsVimentinEpithelial mesenchymal transition (EMT)glioblastomasmall interfering RNA (siRNA)Snail

Identifiers

PMID24966907
PMCPMC4069885
OpenAlexW2241733000

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.