Evidence map›Paper›PMID 32983133›Full record

ArticleFrontiers in immunology2020

LncRNA NEAT1 Targets Fibroblast-Like Synoviocytes in Rheumatoid Arthritis via the miR-410-3p/YY1 Axis.

Yuejiao Wang, Linxin Hou, Xiaowei Yuan, Neili Xu, Shuai Zhao, Lili Yang, Ning Zhang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 8% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. [Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2026
    Article
  4. Article
  5. Review
  6. The Role of Long Non-Coding RNA in Rheumatoid Arthritis.International journal of molecular sciences · 2025
    Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. LncRNAEpigenetics · 2023
    Article
  18. Article
  19. Article
  20. 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.

Yuejiao WangDepartment of Rheumatology and Immunology at Shengjing Hospital of China Medical University, Shenyang, China.
Linxin HouDepartment of Rheumatology and Immunology at Shengjing Hospital of China Medical University, Shenyang, China.
Xiaowei YuanDepartment of Orthopedics at Shengjing Hospital of China Medical University, Shenyang, China.
Neili XuDepartment of Rheumatology and Immunology at Shengjing Hospital of China Medical University, Shenyang, China.
Shuai ZhaoDepartment of Rheumatology and Immunology at Shengjing Hospital of China Medical University, Shenyang, China.
Lili YangDepartment of Rheumatology and Immunology at Shengjing Hospital of China Medical University, Shenyang, China.
Ning ZhangDepartment of Rheumatology and Immunology at Shengjing Hospital of China Medical University, Shenyang, China.
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

LncRNA NEAT1 functions as an oncogene in multiple human cancers. However, its expression and role in fibroblast-like synoviocytes (FLSs) from patients with rheumatoid arthritis (RA) remain unclear. Thus, we investigated the expression of NEAT1 in synovial tissues and FLSs in RA, to determine its role in the development of RA. Quantitative real-time polymerase chain reaction was used to measure the expression of NEAT1. FLS proliferation was evaluated using cell proliferation assays. Flow cytometry was used to analyze cell cycle progression and apoptosis in FLSs. Binding between NEAT1 and miR-410-3p was demonstrated by dual-luciferase assays. We found that NEAT1 was upregulated in synovial tissues and FLSs in RA. Upregulation of NEAT1 promoted cell proliferation, induced S-to G2/M phase transition, and suppressed apoptosis in RA FLSs. NEAT1 directly bound to and negatively modulated miR-410-3p expression, while positively regulating YinYang 1(YY1; a miR-410-3p target). Inhibiting miR-410-3p and upregulating YY1 partially restored the inhibitory role in cell viability induced by the depletion of NEAT1 in RA FLSs. Besides pro-proliferative and anti-apoptotic roles, upregulation of NEAT1 promoted migration, invasion, and inflammatory cytokines secretion in RA FLSs. Taken together, our results suggest that the NEAT1 may serve as a novel diagnostic and therapeutic target for patients with RA.

Indexed as

Gene Expression RegulationRNA InterferenceApoptosisArthritis, RheumatoidCell CycleCell ProliferationCells, CulturedCell SurvivalDisease ProgressionDisease SusceptibilityFibroblastsHumansMicroRNAsRNA, Long NoncodingSynoviocytesYY1 Transcription FactorMicroRNAsMIRN410 microRNA, humanNEAT1 long non-coding RNA, humanRNA, Long NoncodingYY1 protein, humanYY1 Transcription Factorfibroblast-like synoviocytes (FLSs)miR-410-3pNEAT1rheumatoid arthritisYY1

Identifiers

PMID32983133
PMCPMC7485383
OpenAlexW3082265487

What OpenQuestion holds

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Read underepoch 390

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.