Evidence map›Paper›PMID 30654703›Full record

ArticleCell cycle (Georgetown, Tex.)2019

NEAT1 regulates Th2 cell development by targeting STAT6 for degradation.

Shuman Huang, Dong Dong, Yaqian Zhang, Zhuo Chen, Jing Geng, Yulin Zhao

RetractedOpen access · bronzeAbstract readRetracted Publication
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.0field-weighted citation impact, top 13% 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, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. RNA Sequencing of CD4Journal of molecular neuroscience : MN · 2021
    Article
  6. Article
  7. Review
  8. Long non-coding RNA NEAT1-centric gene regulation.Cellular and molecular life sciences : CMLS · 2020
    Review
  9. Review
  10. Review
  11. Review
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Shuman Huanga The Rhinology Department , The First Affiliated Hospital of Zhengzhou University , Zhengzhou , China.
Dong Donga The Rhinology Department , The First Affiliated Hospital of Zhengzhou University , Zhengzhou , China.
Yaqian Zhanga The Rhinology Department , The First Affiliated Hospital of Zhengzhou University , Zhengzhou , China.
Zhuo Chena The Rhinology Department , The First Affiliated Hospital of Zhengzhou University , Zhengzhou , China.
Jing Genga The Rhinology Department , The First Affiliated Hospital of Zhengzhou University , Zhengzhou , China.
Yulin Zhaoa The Rhinology Department , The First Affiliated Hospital of Zhengzhou University , Zhengzhou , China.
First Affiliated Hospital of Zhengzhou University · CNZhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to investigate the role of lncRNA NEAT1 (nuclear enriched abundant transcript 1) in regulating Th2 cell differentiation. The overexpression vectors of NEAT1 and ITCH, and siRNA targeting NEAT1, EZH2 (enhancer of zeste homolog 2) and STAT6 (signal transducer and activator of transcription 6) were transfected into CD4+T cells. The mRNA expressions of ITCH and STAT6 were analyzed by qRT-PCR and western blotting. The levels of Th2 cytokines were detected by ELISA assay. RIP and ChIP assays were performed to analyze the association between NEAT1 and EZH2 as well as EZH2 and STAT6, respectively. Results showed that NEAT1 significantly repressed ITCH expression and increased STAT6 expression as well as the levels of IL-4, IL-5 and IL-13 in CD4+T cells. RIP and ChIP assays revealed that NEAT1 bound to EZH2 and EZH2 was recruited to the promoter region of ITCH in CD4+T cells. Silencing EZH2 significantly promoted STAT6 for ubiquitination. Furthermore, NEAT targeted STAT6 for ubiquitination and elevated levels of Th2 cytokines by regulating EZH2/ITCH axis. In conclusion, our data indicated that NEAT1 promotes Th2 cell differentiation through the EZH2/ITCH/STAT6 axis.

Indexed as

Cell DifferentiationCells, CulturedEnhancer of Zeste Homolog 2 ProteinGene Expression RegulationHumansRepressor ProteinsRNA, Long NoncodingSTAT6 Transcription FactorTh2 CellsUbiquitinationUbiquitin-Protein LigasesEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanITCH protein, humanNEAT1 long non-coding RNA, humanRepressor ProteinsRNA, Long NoncodingSTAT6 protein, humanSTAT6 Transcription FactorUbiquitin-Protein LigasesEZH2ITCHNEAT1STAT6 ubiquitinationTh2 cell differentiation

Identifiers

PMID30654703
PMCPMC6380394
OpenAlexW2909472592

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.