Evidence map›Paper›PMID 27055562›Full record

ArticleExperimental & molecular medicine2016

miR-148a is a downstream effector of X-box-binding protein 1 that silences Wnt10b during adipogenesis of 3T3-L1 cells.

Yoon Mi Cho, Tae-Min Kim, Dae Hun Kim, Dong Hee Kim, Seong-Whan Jeong, Oh-Joo Kwon

Open access · goldAbstract read
In one paragraph

Article in Experimental & molecular medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. The role of WNT10B in physiology and disease: A 10-year update.Frontiers in cell and developmental biology · 2023
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Decrease in MiR-148a Expression During Initiation of Chief Cell Transdifferentiation.Cellular and molecular gastroenterology and hepatology · 2020
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. miR-148a-3p promotes rabbit preadipocyte differentiation by targeting PTEN.In vitro cellular & developmental biology. Animal · 2018
    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

6 authors at 1 institution in 1 country.

Yoon Mi ChoDepartment of Biochemistry, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Tae-Min KimDepartment of Medical Informatics, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Dae Hun KimDepartment of Biochemistry, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0002-9942-8239
Dong Hee KimDepartment of Biochemistry, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Seong-Whan JeongDepartment of Biochemistry, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Oh-Joo KwonDepartment of Biochemistry, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Catholic University of Korea · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wnt10b, an endogenous inhibitor of adipogenesis, maintains preadipocytes in an undifferentiated state by suppressing adipogenic transcription factors. We have previously demonstrated that Wnt10b transcription during adipogenesis is negatively regulated by X-box-binding protein 1 (XBP1), an important transcription factor of the unfolded protein response. In this report, we demonstrate that XBP1s can directly induce the transcription of microRNA-148a, which in turn mediates the silencing of Wnt10b mRNA during adipogenic differentiation of 3T3-L1 cells. Stability of Wnt10b mRNA was found to be significantly increased by knockdown of XBP1s. Using computational algorithms, a set of microRNAs was predicted to bind Wnt10b mRNA, of which microRNA-148a was selected as a potential target for XBP1s. Our results revealed that microRNA-148a could bind to the 3'UTR of Wnt10b mRNA. Its ectopic expression significantly suppressed both Wnt10b expression and β-catenin activity. When we altered the expression of XBP1 in 3T3-L1 cells, microRNA-148a levels changed accordingly. A potential XBP1 response element was found in the promoter region of microRNA-148a, and XBP1s directly bound to this response element as shown by point mutation analysis and chromatin immunoprecipitation assay. In addition, a microRNA-148a mimic significantly restored adipogenic potential in XBP1-deficient 3T3-L1 cells. These findings provide the first evidence that XBP1s can regulate Wnt10b by a post-transcriptional mechanism through directly inducing microRNA-148a.

Indexed as

Gene Expression RegulationGene SilencingRNA Interference3T3-L1 Cells3' Untranslated RegionsAdipocytesAdipogenesisAnimalsBinding SitesDNA-Binding ProteinsHumansMiceMicroRNAsRegulatory Factor X Transcription FactorsRNA StabilityTranscription Factors3' Untranslated RegionsDNA-Binding ProteinsMicroRNAsMirn148 microRNA, mouseRegulatory Factor X Transcription FactorsTranscription FactorsWnt10b protein, mouseWnt ProteinsX-Box Binding Protein 1XBP1 protein, humanXbp1 protein, mouse

Identifiers

PMID27055562
PMCPMC4855278
OpenAlexW2320959715

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.