Evidence map›Paper›PMID 32945470›Full record

ArticleMolecular medicine reports2020

Silencing long non‑coding RNA NEAT1 suppresses the tumorigenesis of infantile hemangioma by competitively binding miR‑33a‑5p to stimulate HIF1α/NF‑κB pathway.

Li Yu, Hong Shu, Lu Xing, Meng-Xing Lv, Li Li, Yu-Cheng Xie, Zhao Zhang, Li Zhang, Yu-Yan Xie

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2020. 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
0.9field-weighted citation impact, top 31% 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, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Non-coding RNA in infantile hemangioma.Pediatric research · 2024
    Review
  6. Puzzling out the role ofNon-coding RNA research · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  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

9 authors at 1 institution in 1 country.

Li YuDepartment of Dermatology, Kunming Children's Hospital, Kunming, Yunnan 650228, P.R. China.
Hong ShuDepartment of Dermatology, Kunming Children's Hospital, Kunming, Yunnan 650228, P.R. China.
Lu XingDepartment of Dermatology, Kunming Children's Hospital, Kunming, Yunnan 650228, P.R. China.
Meng-Xing LvDepartment of Pathology, Kunming Children's Hospital, Kunming, Yunnan 650228, P.R. China.
Li LiDepartment of Institute Pediatrics, Kunming Children's Hospital, Kunming, Yunnan 650228, P.R. China.
Yu-Cheng XieDepartment of Pathology, Kunming Children's Hospital, Kunming, Yunnan 650228, P.R. China.
Zhao ZhangDepartment of Dermatology, Kunming Children's Hospital, Kunming, Yunnan 650228, P.R. China.
Li ZhangDepartment of Dermatology, Kunming Children's Hospital, Kunming, Yunnan 650228, P.R. China.
Yu-Yan XieDepartment of Dermatology, Kunming Children's Hospital, Kunming, Yunnan 650228, P.R. China.
Kunming Children's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infantile hemangioma (IH) is one of the most common vascular tumors that occurs during childhood, but its pathogenesis is currently not completely understood. Even though lncRNA nuclear paraspeckle assembly transcript 1 (NEAT1) plays vital roles in tumorigenesis of malignant tumors, its roles in IH remain unclear. Therefore, we evaluate the function of lncRNA NEAT1 in IH. Reverse transcription‑-quantitative PCR indicated that IH tissues exhibited high expression levels of NEAT1 and hypoxia‑inducible factor 1α (HIF1α), and low expression levels of the microRNA (miR)‑33a‑5p. Small interfering RNA‑mediated depletion of NEAT1 suppressed hemangioma endothelial cell (HemEC) proliferation, migration and invasion. The data suggested that NEAT1 positively regulated HIF1α expression by sponging miR‑33a‑5p in HemECs. miR‑33a‑5p overexpression or HIF1α silencing also acted to suppress HemEC proliferation, migration and invasion. Furthermore, the results indicated that the NEAT1/miR‑33a‑5p/HIF1α axis regulated the NF‑κB signaling pathway. Collectively, the results revealed that depletion of lncRNA NEAT1 suppressed the tumorigenesis of IH by competitively binding miR‑33a‑5p and thereby stimulating the HIF1α/NF‑κB signaling pathway.

Indexed as

3' Untranslated RegionsCell MovementCell ProliferationEndothelial CellsFemaleGene Expression Regulation, NeoplasticHemangiomaHumansHypoxia-Inducible Factor 1, alpha SubunitInfantMaleMicroRNAsNF-kappa BRNA, Long NoncodingRNA, Small InterferingSignal Transduction3' Untranslated RegionsHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitMicroRNAsMIRN33a microRNA, humanNEAT1 long non-coding RNA, humanNF-kappa BRNA, Long NoncodingRNA, Small Interfering

Identifiers

PMID32945470
PMCPMC7453642
OpenAlexW3047577566

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.