Evidence map›Paper›PMID 41547743›Full record

ArticleBMC cancer2026

The potential of MMP14 as a prognostic and immune biomarker in lung cancer.

Jiajia Xiao, Zhenpeng Zhu, Fan Zhang, Xinsheng Wang

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Article in BMC cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Jiajia Xiao *Hebei North University, Zhangjiakou, Hebei Province, 075000, China.
Zhenpeng Zhu *Hebei North University, Zhangjiakou, Hebei Province, 075000, China.
Fan ZhangDepartment of Pathology, The First Affiliated Hospital of Hebei North University, Zhangjiakou, Hebei Province, 075000, China.
Xinsheng WangHebei Key Laboratory of Pathogenic Mechanisms and Diagnosis & Treatment Technologies for Lung Microbiome, The First Affiliated Hospital of Hebei North University, Zhangjiakou, Hebei Province, 075000, China. wangxinsheng@hbbfyfy.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrecision therapy and prognostic assessment are crucial for improving the quality of life of patients with lung cancer. While NSUN2-mediated m⁵C RNA methylation is involved in multiple malignancies, the role of its downstream target MMP14 in lung adenocarcinoma remains undefined.

methodsUsing the A549 cell line as the research object, we established a stable NSUN2 knockdown model. Differentially expressed gene MMP14 was identified through RNA-seq, and its expression was validated by quantitative real-time polymerase chain reaction (RT-qPCR). Combined with The Cancer Genome Atlas (TCGA) and multi-database integrated analysis, we thoroughly elucidated the molecular regulatory mechanisms (focusing on RNA methylation-related pathways) and clinical value of MMP14 in LUAD.

resultsOur findings demonstrate that MMP14 is overexpressed in LUAD and multiple other malignancies, and that its elevated expression is significantly associated with poor prognosis and advanced tumor stage. In LUAD, MMP14 RNA methylation levels are positively correlated with mRNA expression, while DNA promoter methylation is closely linked to tumor progression and lymph node metastasis. MMP14 expression is regulated by NSUN2, a key m⁵C methyltransferase, and functionally participates in diverse tumor-associated biological processes. Notably, MMP14 expression correlates with immune cell infiltration, including macrophages and T cells, as well as with immune checkpoint molecules such as PD-1 and PD-L1, highlighting its potential role in shaping the tumor immune microenvironment.

conclusionMMP14, a key NSUN2-regulated molecule in LUAD, represents a potential target for precision diagnosis and therapy and may provide new insights into improving overall survival in LUAD.

Indexed as

Adenocarcinoma of LungBiomarkers, TumorLung NeoplasmsMatrix Metalloproteinase 14Cell Line, TumorDNA MethylationGene Expression Regulation, NeoplasticHumansMethyltransferasesPrognosisRNA MethylationTumor MicroenvironmentBiomarkers, TumorMatrix Metalloproteinase 14MethyltransferasesMMP14 protein, humanNSUN2 protein, humanLung adenocarcinomaMethylationMMP14NSUN2Prognostic assessmentRNA-seqSingle-cell sequencingTumor heterogeneity

Identifiers

PMID41547743
PMCPMC12910734

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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.