Evidence map›Paper›PMID 31240814›Full record

ArticleJournal of cellular and molecular medicine2019

Long non-coding RNA LINC00526 represses glioma progression via forming a double negative feedback loop with AXL.

Jian Yan, Chunhua Xu, Youping Li, Bin Tang, Shenhao Xie, Tao Hong, Erming Zeng

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
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  10. miR-454-3p promotes of human glioma cell growth by targeting EGR3.Experimental and therapeutic medicine · 2019
    Article
  11. Article
  12. The Emerging Role of lncRNAs in Spinal Cord Injury.BioMed research international · 2019
    Review
  13. 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

7 authors at 1 institution in 1 country.

Jian YanDepartment of Neurosurgery, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Chunhua XuDepartment of Neurosurgery, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Youping LiDepartment of Neurosurgery, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Bin TangDepartment of Neurosurgery, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Shenhao XieDepartment of Neurosurgery, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Tao HongDepartment of Neurosurgery, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Erming ZengDepartment of Neurosurgery, The First Affiliated Hospital of Nanchang University, Nanchang, China.ORCID 0000-0002-7466-6038
Nanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioma is the most common primary intracranial carcinoma with extremely poor prognosis. The significances of long non-coding RNA (lncRNA) involved in glioma have been started revealed. However, the expression, roles and molecular mechanisms of most lncRNAs in glioma are still unknown. In this study, we identified a novel lncRNA LINC00526, which is significantly low expressed in glioma. Low expression of LINC00526 is correlated with aggravation and poor survival in glioma. Functional assays revealed that ectopic expression of LINC00526 inhibits glioma cell proliferation, migration, and invasion. LINC00526 silencing promotes glioma cell proliferation, migration and invasion. Mechanistically, we found that LINC00526 directly interacts with EZH2, represses the binding of EZH2 to AXL promoter, attenuates the transcriptional activating roles of EZH2 on AXL, and therefore represses AXL expression. Via repressing AXL, LINC00526 further represses PI3K/Akt/NF-κB signalling. Intriguingly, we identified that NFKB1 and NFKB2 directly binds LINC00526 promoter and represses LINC00526 transcription. We further found that via activating NF-κB signalling, AXL represses LINC00526 transcription. Therefore, LINC00526/EZH2/AXL/PI3K/Akt/NF-κB form a feedback loop in glioma. Analysis of the TCGA data revealed that the expression of LINC00526 is inversely correlated with that of AXL in glioma tissues. In addition, functional rescue assays revealed that the tumour suppressive roles of LINC00526 are dependent on the negative regulation of AXL. Collectively, our data identified LINC00526 as a tumour suppressor in glioma via forming a double negative feedback loop with AXL. Our data also suggested LINC00526 as a potential prognostic biomarker and therapeutic candidate for glioma.

Indexed as

Disease ProgressionFeedback, PhysiologicalAxl Receptor Tyrosine KinaseBrain NeoplasmsCell Line, TumorCell MovementCell ProliferationEnhancer of Zeste Homolog 2 ProteinGene Expression Regulation, NeoplasticGene SilencingGliomaHumansNeoplasm InvasivenessNF-kappa BProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesAXL protein, humanAxl Receptor Tyrosine KinaseEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanNF-kappa BProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesRNA, Long NoncodingAXLfeedback loopgliomalong non-coding RNAprogression

Identifiers

PMID31240814
PMCPMC6653591
OpenAlexW2956052367

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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.