Evidence map›Paper›PMID 36920524›Full record

ArticleDiabetologia2023

Deficiency of WTAP in islet beta cells results in beta cell failure and diabetes in mice.

Xinzhi Li, Ying Yang, Zhenzhi Li, Yuqin Wang, Jingting Qiao, Zheng Chen

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Diabetologia, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
9.5field-weighted citation impact, top 1% 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

21 citing papers in PubMed, 30 citations in OpenAlex.

  1. RNA mActa pharmacologica Sinica · 2026
    Review
  2. Article
  3. WTAP mediated mScience China. Life sciences · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Targeting RNA adenosine editing and modification enzymes for RNA therapeutics.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  11. Review
  12. Review
  13. Exploring the methyl-verse: Dynamic interplay of epigenome and m6A epitranscriptome.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  14. Review
  15. The latest progression of N6-methyladenosine (mFrontiers in endocrinology · 2025
    Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. The role of mFrontiers in endocrinology · 2023
    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 2 institutions in 1 country.

Xinzhi LiHIT Center for Life Sciences, School of Life Science and Technology, Harbin Institute of Technology, Harbin, China.
Ying YangHIT Center for Life Sciences, School of Life Science and Technology, Harbin Institute of Technology, Harbin, China.
Zhenzhi LiHIT Center for Life Sciences, School of Life Science and Technology, Harbin Institute of Technology, Harbin, China.
Yuqin WangHIT Center for Life Sciences, School of Life Science and Technology, Harbin Institute of Technology, Harbin, China.
Jingting QiaoDepartment of Endocrinology and Metabolism, Tianjin Medical University General Hospital, Tianjin, China.
Zheng ChenHIT Center for Life Sciences, School of Life Science and Technology, Harbin Institute of Technology, Harbin, China. chenzheng@hit.edu.cn.ORCID http://orcid.org/0000-0001-7129-6644
Harbin Institute of Technology · CNTianjin Medical University General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aims/hypothesisN

methodsIslet beta cell-specific Wtap-knockout and beta cell-specific Mettl3-overexpressing mice were generated for this study. Blood glucose, glucose tolerance, serum insulin, glucose-stimulated insulin secretion (both in vivo and in vitro), insulin levels, glucagon levels and beta cell apoptosis were examined. RNA-seq and MeRIP-seq were performed, and the data were well analysed.

resultsWTAP was downregulated in islet beta cells in type 2 diabetes, due to lipotoxicity and chronic inflammation, and islet beta cell-specific deletion of Wtap (Wtap-betaKO) induced beta cell failure and diabetes. Wtap-betaKO mice showed severe hyperglycaemia (above 20 mmol/l [360 mg/dl]) from 8 weeks of age onwards. Mechanistically, WTAP deficiency decreased m CONCLUSIONS/

interpretationWTAP plays a key role in maintaining beta cell function by regulating m DATA AVAILABILITY: The RNA-seq and MeRIP-seq datasets generated during the current study are available in the Gene Expression Omnibus database repository ( https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE215156 ; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE215360 ).

Indexed as

Diabetes Mellitus, Type 2InsulinsAnimalsGlucoseMethyltransferasesMiceRNA, MessengerGlucoseInsulinsMethyltransferasesRNA, MessengerHyperglycaemiaInsulin secretionIslet beta cellsMETTL3N 6-methyladenosineWTAP

Identifiers

PMID36920524
OpenAlexW4324311554

What Socratic 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 Socratic graph.