Evidence map›Paper›PMID 40319192›Full record

ArticleNPJ precision oncology2025

FOXA1-dependent NSUN2 facilitates the advancement of prostate cancer by preserving TRIM28 mRNA stability in a m5C-dependent manner.

Zhenda Wang, Abudurexiti Mierxiati, Wenkai Zhu, Tian Li, Hua Xu, Fangning Wan, Dingwei Ye

Abstract read
In one paragraph

Article in NPJ precision oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. CSDE1 Drives Glycolysis and the Progression of Prostate Cancer Through RAC1-Dependent RAS/MAPK Activation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  2. Review
  3. Review
  4. NSUN2-Mediated mInternational journal of general medicine · 2026
    Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Roles and mechanisms of NSUN2-mediated RNA mFrontiers in immunology · 2025
    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

7 authors.

Zhenda Wang *Department of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Abudurexiti Mierxiati *Department of Urology, Gongli Hospital of Shanghai Pudong New Area, Shanghai, China.
Wenkai ZhuDepartment of Urology, First People's Hospital of Kashi, Kashi, China.
Tian LiTianjin Medical University, Tianjin, China. fmmult@foxmail.com.
Hua XuDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China. norman.xu@hotmail.com.
Fangning WanDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China. fnwan06@fudan.edu.cn.
Dingwei YeDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China. dingwei_ye@fudan.edu.cn.

Funding

Grants from the National Key Research and Development Program of China No.2019YFC1316005National Natural Science Foundation of China No.82473505, No.81802525 and No.81902568Shanghai Sailing Program No.19YF1409700Shanghai Science and Technology Committee No.20ZR1413100, No.18511108000
6 · The paper itself

Abstract

RNA epigenetics is gaining increased attention for its role in the initiation, metastasis, and drug resistance of tumors. These studies have primarily focused on m6A modification. However, despite being the second most abundant modification found in RNA, the role of m5C modification in prostate cancer remains largely unexplored. Here, we predict an RNA m5C methyltransferase, NSUN2, as a potential therapeutic target for prostate cancer using various bioinformatics approaches, and verify the potential of NSUN2 as a target through multiple preclinical models. Mechanistically, NSUN2 enhances the stability of TRIM28 mRNA by adding m5C modification, promoting the expression of TRIM28. Concurrently, FOXA1, a prostate cancer lineage-specific transcription factor, transcriptionally activates the expression of NSUN2. Our study confirms the clinical potential of targeting RNA epigenetics for the treatment of prostate cancer and elucidates, mechanistically, how RNA epigenetics participates in the complex biological activities within tumors via the FOXA1-NSUN2-TRIM28 axis.

Identifiers

PMID40319192
PMCPMC12049421

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.