ArticleNaunyn-Schmiedeberg's archives of pharmacology2026
The METTL3/IGF2BP1 axis-mediated m6 A modification of TRIM11 mRNA suppresses ferroptosis and accelerates malignant progression in non-small cell lung cancer cells by degrading ACSL4.
Article in Naunyn-Schmiedeberg's archives of pharmacology, 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
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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.
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Who cites it
2 citing papers in PubMed.
- Bidirectional regulation of the ubiquitin-RNA modification axis in cancer.Frontiers in oncology · 2026Review
- Nrf2 functions as a biomarker and therapeutic target in lung cancer based on bibliometric analysis and molecular mechanisms.Discover oncology · 2025Article
Corrections and comments
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Tripartite motif-containing motif 11 (TRIM11) possesses a pro-tumorigenic properties in non-small cell lung cancer (NSCLC). However, the determinants that drive TRIM11 dysregulation remains to be uncovered. Effect on cell functions was assessed by detecting cell apoptosis, proliferation, viability, ferroptosis, and invasive and migratory capacities. Evaluation of in vivo activity was performed using mouse xenograft studies. Relationship between TRIM11 and METTL3 or IGF2BP1 was predicted by bioinformatics and confirmed by RNA immunoprecipitation experiments or luciferase assays. The regulation of TRIM11 in ACSL4 protein was tested by IP experiment and protein stability analysis. TRIM11 was overexpressed in NSCLC, and its high expression tended to result in poor prognosis and enhanced tumor grade. Functionally, TRIM11 disruption suppresses the malignant progression of NSCLC cells by promoting cancer cell apoptosis and ferroptosis and repressing invasion, proliferation, and migration. Mechanistically, METTL3 enhances m6A modification of TRIM11 mRNA via an IGF2BP1/m6A manner. Inhibition of METTL3 reduced TRIM11 to promote NSCLC cell ferroptosis and suppress malignant progression in vitro, as well as to mediate xenograft growth inhibition in vivo. Additionally, TRIM11 degraded ACSL4 through K63-linked ubiquitination to affect the malignant progression and ferroptosis of NSCLC cells. These findings indicate that the METTL3/IGF2BP1 axis-mediated m6A methylation of TRIM11 mRNA is responsible for NSCLC malignant progression of NSCLC. Our study is instrumental for the development of TRIM11-basic therapies for NSCLC.
Indexed as
Identifiers
40668412What 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.