Evidence map›Paper›PMID 37599359›Full record

ArticleJournal of experimental & clinical cancer research : CR2023

P300/SP1 complex mediating elevated METTL1 regulates CDK14 mRNA stability via internal m7G modification in CRPC.

Mingpeng Zhang, Duo Kan, Boya Zhang, Xueqiao Chen, Chun Wang, Songmao Chen, Wenlong Gao, Zhao Yang, Yang Li, Yutong Chen and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

40 citing papers in PubMed, 50 citations in OpenAlex.

  1. GnRH Promotes Gonadotropin Synthesis and Secretion in the Bovine Anterior Pituitary by Inhibiting METTL1-Mediated m7G Modification of FOXO1 mRNA.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
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  6. METTL1-mediated mOncogene · 2026
    Article
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  8. iScience · 2026
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  18. WTAP-mediated mScience China. Life sciences · 2025
    Article
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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

14 authors at 2 institutions in 1 country.

Mingpeng Zhang *Tianjin Institute of Urology, the Second Hospital of Tianjin Medical University, Tianjin, 300211, China.
Duo Kan *Tianjin Institute of Urology, the Second Hospital of Tianjin Medical University, Tianjin, 300211, China.
Boya Zhang *Bone and Soft Tissue Department, The Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital, Zhengzhou, 450000, China.
Xueqiao Chen *Tianjin Institute of Urology, the Second Hospital of Tianjin Medical University, Tianjin, 300211, China.
Chun WangTianjin Institute of Urology, the Second Hospital of Tianjin Medical University, Tianjin, 300211, China.
Songmao ChenTianjin Institute of Urology, the Second Hospital of Tianjin Medical University, Tianjin, 300211, China.
Wenlong GaoTianjin Institute of Urology, the Second Hospital of Tianjin Medical University, Tianjin, 300211, China.
Zhao YangTianjin Institute of Urology, the Second Hospital of Tianjin Medical University, Tianjin, 300211, China.
Yang LiTianjin Institute of Urology, the Second Hospital of Tianjin Medical University, Tianjin, 300211, China.
Yutong ChenTianjin Institute of Urology, the Second Hospital of Tianjin Medical University, Tianjin, 300211, China.
Shimiao ZhuTianjin Institute of Urology, the Second Hospital of Tianjin Medical University, Tianjin, 300211, China.
Simeng WenTianjin Institute of Urology, the Second Hospital of Tianjin Medical University, Tianjin, 300211, China.
Yuanjie NiuTianjin Institute of Urology, the Second Hospital of Tianjin Medical University, Tianjin, 300211, China. niuyuanjie9317@163.com.
Zhiqun ShangTianjin Institute of Urology, the Second Hospital of Tianjin Medical University, Tianjin, 300211, China. zhiqun_shang@tmu.edu.cn.
Second Hospital of Tianjin Medical University · CNZhengzhou University · CN

Funding

National Natural Science Foundation of China 81972654National Natural Science Foundation of China 82061160493National Natural Science Foundation of China 82072851National Natural Science Foundation of China 82172759National Natural Science Foundation of China 82172829National Natural Science Foundation of China 82272918National Natural Science Foundation of China 82273262
6 · The paper itself

Abstract

backgroundN7-methylguanosine (m7G) modification is, a more common epigenetic modification in addition to m6A modification, mainly found in mRNA capsids, mRNA interiors, transfer RNA (tRNA), pri-miRNA, and ribosomal RNA (rRNA). It has been found that m7G modifications play an important role in mRNA transcription, tRNA stability, rRNA processing maturation, and miRNA biosynthesis. However, the role of m7G modifications within mRNA and its "writer" methyltransferase 1(METTL1) in tumors, particularly prostate cancer (PCa), has not been revealed.

methodsThe differential expression level of METTL1 between hormone-sensitive prostate cancer (HSPC) and castrate-resistant prostate cancer (CRPC) was evaluated via RNA-seq and in vitro experiments. The effects of METTL1 on CRPC progression were investigated through in vitro and in vivo assays. The upstream molecular mechanism of METTL1 expression upregulation and the downstream mechanism of its action were explored via Chromatin Immunoprecipitation quantitative reverse transcription polymerase chain reaction (CHIP-qPCR), Co-immunoprecipitation (Co-IP), luciferase reporter assay, transcriptome-sequencing, m7G AlkAniline-Seq, and mRNA degradation experiments, etc. RESULTS AND

conclusionHere, we found that METTL1 was elevated in CRPC and that patients with METTL1 elevation tended to have a poor prognosis. Functionally, the knockdown of METTL1 in CRPC cells significantly limited cell proliferation and invasive capacity. Mechanistically, we unveiled that P300 can form a complex with SP1 and bind to the promoter region of the METTL1 gene via SP1, thereby mediating METTL1 transcriptional upregulation in CRPC. Subsequently, our findings indicated that METTL1 leads to enhanced mRNA stability of CDK14 by adding m7G modifications inside its mRNA, ultimately promoting CRPC progression.

Indexed as

MethyltransferasesProstatic Neoplasms, Castration-ResistantSp1 Transcription FactorCell ProliferationChromatin ImmunoprecipitationCyclin-Dependent KinasesHumansMaleMicroRNAsRNA StabilityCDK14 protein, humanCyclin-Dependent KinasesMethyltransferasesMETTL1 protein, humanMicroRNAsSp1 Transcription FactorCDK14CRPCm7GMETTL1P300/SP1 complex

Identifiers

PMID37599359
PMCPMC10440916
OpenAlexW4386019143

What OpenQuestion holds

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Registered trials

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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.