Evidence map›Paper›PMID 32094308›Full record

ArticleMolecular and cellular biology2020

E2F6-Mediated Downregulation of MIR22HG Facilitates the Progression of Laryngocarcinoma by Targeting the miR-5000-3p/FBXW7 Axis.

Hui Chen, Mudunov Ali, Azizyan Ruben, Dimitry Stelmakh, Maksim Pak

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Review
  3. Biomedicines · 2024
    Article
  4. Article
  5. Molecular insights and clinical implications for the tumor suppressor role of SCFBiochimica et biophysica acta. Reviews on cancer · 2024
    Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. 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

5 authors at 2 institutions in 1 country.

Hui ChenI. M. Sechenov First Moscow State Medical University, Moscow, Russian Federation.
Mudunov AliN. N. Blokhin National Medical Research Center of the Oncology of the Ministry of Health of the Russian Federation, Moscow, Russian Federation ali.mudunov@inbox.ru.
Azizyan RubenN. N. Blokhin National Medical Research Center of the Oncology of the Ministry of Health of the Russian Federation, Moscow, Russian Federation.
Dimitry StelmakhN. N. Blokhin National Medical Research Center of the Oncology of the Ministry of Health of the Russian Federation, Moscow, Russian Federation.
Maksim PakN. N. Blokhin National Medical Research Center of the Oncology of the Ministry of Health of the Russian Federation, Moscow, Russian Federation.
Ministry of Health of the Russian Federation · RUSechenov University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, abundant evidence has clarified that long noncoding RNAs (lncRNAs) play an oncogenic or anticancer role in the tumorigenesis and development of diverse human cancers. Described as a crucial regulator in some cancers, MIR22HG has not yet been studied in laryngocarcinoma and therefore the underlying regulatory role of MIR22HG in laryngocarcinoma is worth detecting. In this study, MIR22HG expression in laryngocarcinoma cells was confirmed to be downregulated, and upregulated MIR22HG expression led to suppressive effects on laryngocarcinoma cell proliferation and migration. Molecular mechanism assays revealed that MIR22HG sponges miR-5000-3p in laryngocarcinoma cells. Besides, decreased expression of miR-5000-3p suppressed laryngocarcinoma cell proliferation and migration. Moreover, the FBXW7 gene was reported to be a downstream target gene of miR-5000-3p in laryngocarcinoma cells. More importantly, rescue assays verified that FBXW7 depletion or miR-5000-3p upregulation countervailed the repressive effects of MIR22HG overexpression on laryngocarcinoma progression. In addition, E2F6 was proved to be capable of inhibiting MIR22HG transcription in laryngocarcinoma cells. To sum up, E2F6-induced downregulation of MIR22HG promotes laryngocarcinoma progression through the miR-5000-3p/FBXW7 axis.

Indexed as

Cell Line, TumorCell ProliferationDisease ProgressionDown-RegulationE2F6 Transcription FactorF-Box-WD Repeat-Containing Protein 7Gene Expression Regulation, NeoplasticHumansLaryngeal NeoplasmsMicroRNAsNeoplasm InvasivenessE2F6 protein, humanE2F6 Transcription FactorF-Box-WD Repeat-Containing Protein 7FBXW7 protein, humanMicroRNAsMIRN22 microRNA, humanMIRN5000 microRNA, humanE2F6FBXW7laryngocarcinomaMIR22HGmiR-5000-3p

Identifiers

PMID32094308
PMCPMC7189097
OpenAlexW3008163637

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.