Evidence map›Paper›PMID 37108067›Full record

ArticleInternational journal of molecular sciences2023

YTHDF1 Promotes Bladder Cancer Cell Proliferation via the METTL3/YTHDF1-RPN2-PI3K/AKT/mTOR Axis.

Junlong Zhu, Hang Tong, Yan Sun, Tinghao Li, Guang Yang, Weiyang He

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 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. mFrontiers in cell and developmental biology · 2026
    Review
  7. Article
  8. Review
  9. Unraveling the dual role of METTL3-mediated mCancer biology & therapy · 2025
    Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. YTHDF1 in Tumor Cell Metabolism: An Updated Review.Molecules (Basel, Switzerland) · 2023
    Review
  20. 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.

Junlong ZhuDepartment of Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Hang TongDepartment of Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Yan SunDepartment of Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Tinghao LiDepartment of Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Guang YangDepartment of Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Weiyang HeDepartment of Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Chongqing Medical University · CNFirst Affiliated Hospital of Chongqing Medical University · CN

Funding

Hubin Yin CSTB2022BSXM-JCX0037
6 · The paper itself

Abstract

N6-methyladenosine (m6A) is the most common mRNA modification and it plays a critical role in tumor progression, prognoses and therapeutic response. In recent years, more and more studies have shown that m6A modifications play an important role in bladder carcinogenesis and development. However, the regulatory mechanisms of m6A modifications are complex. Whether the m6A reading protein YTHDF1 is involved in the development of bladder cancer remains to be elucidated. The aims of this study were to determine the association between METTL3/YTHDF1 and bladder cancer cell proliferation and cisplatin resistance to explore the downstream target genes of METTL3/YTHDF1 and to explore the therapeutic implications for bladder cancer patients. The results showed that the reduced expression of METTL3/YTHDF1 could lead to decreased bladder cancer cell proliferation and cisplatin sensitivity. Meanwhile, overexpression of the downstream target gene, RPN2, could rescue the effect of reduced METTL3/YTHDF1 expression on bladder cancer cells. In conclusion, this study proposes a novel METTL3/YTHDF1-RPN2-PI3K/AKT/mTOR regulatory axis that affects bladder cancer cell proliferation and cisplatin sensitivity.

Indexed as

HexosyltransferasesUrinary Bladder NeoplasmsCell ProliferationCisplatinHumansMethyltransferasesPhosphatidylinositol 3-KinasesProteasome Endopeptidase ComplexProto-Oncogene Proteins c-aktRNA-Binding ProteinsTOR Serine-Threonine KinasesCisplatinHexosyltransferasesMethyltransferasesMETTL3 protein, humanMTOR protein, humanPhosphatidylinositol 3-KinasesProteasome Endopeptidase ComplexProto-Oncogene Proteins c-aktRNA-Binding ProteinsRPN2 protein, humanTOR Serine-Threonine KinasesYTHDF1 protein, humanbladder cancercell proliferationdrug sensitivitym6AN6-methyladenosine

Identifiers

PMID37108067
PMCPMC10139185
OpenAlexW4363676519

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.