ArticleBMC cancer2026
The potential of MMP14 as a prognostic and immune biomarker in lung cancer.
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.
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.
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.
Who cites it
2 citing papers in PubMed.
- Radiomics: Current Applications and Future Directions.MedComm · 2026Review
- [Mechanisms of Macrophage Efferocytosis-driven Remodeling of Lung Cancer Microenvironment Structure and Angiogenesis and Prospects for Clinical Intervention].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
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
Identifiers
What OpenQuestion holds
Registered trials
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.