Evidence map›Paper›PMID 41165830›Full record

ArticleCellular and molecular life sciences : CMLS2025

m6A-mediated upregulation of miR-3690 drives HNSCC progression by regulating nuclear-cytoplasmic signaling pathway.

Yujuan Zhou, Qiang Huang, Xiaohui Yuan, Ye Xu, Chengzhi Xu, Yang Guo, Liang Zhou

Abstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Yujuan Zhou *Department of Otorhinolaryngology, Eye & ENT Hospital, Fudan University, Shanghai, China.
Qiang Huang *Department of Otorhinolaryngology, Eye & ENT Hospital, Fudan University, Shanghai, China.ORCID http://orcid.org/0000-0002-5455-9454
Xiaohui Yuan *Department of Otorhinolaryngology, Eye & ENT Hospital, Fudan University, Shanghai, China.
Ye XuLiver Cancer Institute, Zhongshan Hospital, Fudan University and Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of Education, Shanghai, China.
Chengzhi XuDepartment of Otorhinolaryngology, Eye & ENT Hospital, Fudan University, Shanghai, China. chengzhi_xu@fudan.edu.cn.
Yang GuoDepartment of Otorhinolaryngology, Eye & ENT Hospital, Fudan University, Shanghai, China. guoyangls@126.com.
Liang ZhouDepartment of Otorhinolaryngology, Eye & ENT Hospital, Fudan University, Shanghai, China. liang.zhou@fdeent.org.ORCID http://orcid.org/0009-0004-5658-8699

Funding

National Natural Science Foundation of China 81972529National Natural Science Foundation of China 82372972National Natural Science Foundation of China 82403387Science and Technology Commission of Shanghai Municipality 19411961300Shanghai Sailing Program 21YF1405600Shanghai Sailing Program 23YF1404700
6 · The paper itself

Abstract

MicroRNAs (miRNAs) are involved in carcinogenesis. However, the biological roles and underlying mechanism of miR-3690 in head and neck squamous cell carcinoma (HNSCC) progression are far from elucidated. In this study, we found that the expression level of miR-3690 in HNSCC tissues was significantly higher and correlated with poor clinical prognosis. HNSCC cells proliferation, migration, and invasion were promoted by miR-3690 overexpression, both in vitro and in vivo. Mechanistically, miRNA pulldown DNA-seq and luciferase reporter assays revealed that miR-3690 could directly activate CKS2 expression through targeting its promoter. Meanwhile, RNA pull down and mass spectrometry (MS) analysis suggested that upregulation of CKS2 by miR-3690 correlated with increased BPTF occupancy and H3K4me3 at CKS2 promoter. Additionally, luciferase reporter assays showed that miR-3690 facilitated Wnt/β-catenin signaling in HNSCC by repressing NKD1 expression through directly targeting its 3'-UTR. Finally, methylated RNA Immunoprecipitation (meRIP) and RNA pull down indicated that METTL3 and METTL14-mediated m6A modification accelerated pri-miR-3690 maturation through regulating the processing of pri-miR-3690 by DGCR8. In conclusion, miR-3690 may be a prognostic indicator and potential therapeutic target for HNSCC.

Indexed as

AdenosineHead and Neck NeoplasmsMicroRNAsRNA MethylationSquamous Cell Carcinoma of Head and NeckCDC2-CDC28 KinasesCell Cycle ProteinsCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansPromoter Regions, GeneticSignal TransductionTranscription, GeneticUp-RegulationAdenosineCDC2-CDC28 KinasesCell Cycle ProteinsCKS2 protein, humanMicroRNAsN-methyladenosineBPTFCKS2m6AmiR-3690NKD1

Identifiers

PMID41165830
PMCPMC12575877

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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.