Evidence map›Paper›PMID 33533172›Full record

ArticleJournal of cellular and molecular medicine2021

Kinase GSK3β functions as a suppressor in colorectal carcinoma through the FTO-mediated MZF1/c-Myc axis.

Zeyan Zhang, Qianfu Gao, Shanchao Wang

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.6field-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

23 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Regulations of mFrontiers of medicine · 2024
    Review
  7. Review
  8. Review
  9. Ubiquitination and deubiquitination in the regulation of NJournal of molecular medicine (Berlin, Germany) · 2024
    Review
  10. Article
  11. Epigenetic modification of mMolecular cancer · 2023
    Review
  12. Review
  13. Review
  14. The emerging role of mFrontiers in cell and developmental biology · 2023
    Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Role of m6A writers, erasers and readers in cancer.Experimental hematology & oncology · 2022
    Review
  20. 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

3 authors at 1 institution in 1 country.

Zeyan ZhangAnorectal Department, Linyi People' s Hospital, Linyi, China.ORCID 0000-0003-3351-6591
Qianfu GaoAnorectal Department, Linyi People' s Hospital, Linyi, China.ORCID 0000-0002-2742-5987
Shanchao WangAnorectal Department, Linyi People' s Hospital, Linyi, China.ORCID 0000-0001-6616-6693
Linyi People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal carcinoma (CRC) poses heavy burden to human health and has an increasing incidence. Currently, the existing biomarkers for CRC bring about restrained clinical benefits. GSK3β is reported to be a novel therapeutic target for this disease but with undefined molecular mechanisms. Thus, we aimed to investigate the regulatory effect of GSK3β on CRC progression via FTO/MZF1/c-Myc axis. Firstly, the expression patterns of GSK3β, FTO, MZF1 and c-Myc were determined after sample collection. Lowly expressed GSK3β but highly expressed FTO, MZF1 and c-Myc were found in CRC. After transfection of different overexpressed and interference plasmids, the underlying mechanisms concerning GSK3β in CRC cell functions were analysed. Additionally, the effect of GSK3β on FTO protein stability was assessed followed by detection of MZF1 m6A modification and MZF1-FTO interaction. Mechanistically, GSK3β mediated ubiquitination of demethylase FTO to reduce FTO expression. Besides, GSK3β inhibited MZF1 expression by mediating FTO-regulated m6A modification of MZF1 and then decreased the proto-oncogene c-Myc expression, thus hampering CRC cell proliferation. We also carried out in vivo experiment to verify the regulatory effect of GSK3β on CRC via FTO-mediated MZF1/c-Myc axis. It was found that GSK3β inhibited CRC growth in vivo which was reversed by overexpressing c-Myc. Taken together, our findings indicate that GSK3β suppresses the progression of CRC through FTO-regulated MZF1/c-Myc axis, shedding light onto a new possible pathway by which GSK3β regulates CRC.

Indexed as

Signal TransductionAlpha-Ketoglutarate-Dependent Dioxygenase FTOAnimalsCell Line, TumorColorectal NeoplasmsDisease Models, AnimalGene Expression Regulation, NeoplasticGlycogen Synthase Kinase 3 betaHumansKruppel-Like Transcription FactorsMiceModels, BiologicalProto-Oncogene MasProto-Oncogene Proteins c-mycXenograft Model Antitumor AssaysAlpha-Ketoglutarate-Dependent Dioxygenase FTOFTO protein, humanGlycogen Synthase Kinase 3 betaKruppel-Like Transcription FactorsMAS1 protein, humanMZF1 protein, humanProto-Oncogene MasProto-Oncogene Proteins c-myccolorectal carcinomafat mass and obesity-associated proteinglycogen synthase kinase 3 betamyeloid zinc finger 1N6-methyladenosine

Identifiers

PMID33533172
PMCPMC7933972
OpenAlexW3127946710

What OpenQuestion holds

Textmetadata
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.