Evidence map›Paper›PMID 36982885›Full record

ArticleInternational journal of molecular sciences2023

MiR-424/TGIF2-Mediated Pro-Fibrogenic Responses in Oral Submucous Fibrosis.

Ming-Yung Chou, Pei-Ling Hsieh, Shih-Chi Chao, Yi-Wen Liao, Cheng-Chia Yu, Chang-Yi Tsai

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.1field-weighted citation impact, top 9% 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, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Oral submucous fibrosis: pathogenesis and therapeutic approaches.International journal of oral science · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Crosstalk of ubiquitin system and non-coding RNA in fibrosis.International journal of biological sciences · 2024
    Review
  11. Review
  12. Review
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

6 authors at 4 institutions in 1 country.

Ming-Yung ChouSchool of Dentistry, Chung Shan Medical University, Taichung 40201, Taiwan.
Pei-Ling HsiehDepartment of Anatomy, School of Medicine, China Medical University, Taichung 404333, Taiwan.ORCID 0000-0002-4190-6795
Shih-Chi ChaoInstitute of Oral Sciences, Chung Shan Medical University, Taichung 40201, Taiwan.ORCID 0000-0002-0920-9340
Yi-Wen LiaoInstitute of Oral Sciences, Chung Shan Medical University, Taichung 40201, Taiwan.
Cheng-Chia YuSchool of Dentistry, Chung Shan Medical University, Taichung 40201, Taiwan.
Chang-Yi TsaiDepartment of Otorhinolaryngology-Head and Neck Surgery, Changhua Christian Hospital, Changhua 500, Taiwan.
Chung Shan Medical University Hospital · TWChanghua Christian Hospital · TWChina Medical University · TWLuodong Poh-Ai Hospital · TW

Funding

Chung Shan Medical University Hospital CSH-2022-D-004
6 · The paper itself

Abstract

Oral submucous fibrosis (OSF) has been recognized as a potentially malignant disorder and is characterized by inflammation and the deposition of collagen. Among various regulators of fibrogenesis, microRNAs (miR) have received great attention but the detailed mechanisms underlying the miR-mediated modulations remain largely unknown. Here, we showed that miR-424 was aberrantly overexpressed in OSF tissues, and then we assessed its functional role in the maintenance of myofibroblast characteristics. Our results demonstrated that the suppression of miR-424 markedly reduced various myofibroblast activities (such as collagen contractility and migration ability) and downregulated the expression of fibrosis markers. Moreover, we showed that miR-424 exerted this pro-fibrosis property via direct binding to TGIF2, an endogenous repressor of the TGF-β signaling. In addition, our findings indicated that overexpression of miR-424 activated the TGF-β/Smad pathway, leading to enhanced myofibroblast activities. Altogether, our data revealed how miR-424 contributed to myofibroblast transdifferentiation, and targeting the miR-424/TGIF2 axis may be a viable direction for achieving satisfactory results from OSF treatment.

Indexed as

MicroRNAsOral Submucous FibrosisCollagenFibrosisHomeodomain ProteinsHumansMouth MucosaMyofibroblastsRepressor ProteinsTransforming Growth Factor betaCollagenHomeodomain ProteinsMicroRNAsMIRN424 microrna, humanRepressor ProteinsTGIF2 protein, humanTransforming Growth Factor betamiR-424oral submucous fibrosisTGIF2

Identifiers

PMID36982885
PMCPMC10053232
OpenAlexW4327968787

What OpenQuestion holds

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LicenceCC BY
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.