ArticleBMC musculoskeletal disorders2026
The METTL3-IGF2BP3 axis drives osteosarcoma progression by enhancing ID1 mRNA stability.
Article in BMC musculoskeletal disorders, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 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
3 citing papers in PubMed.
- METTL3 promotes proliferation and invasion and inhibits ferroptosis in hepatocellular carcinoma by mediating m6A methylation modification of NUPR1.Molecular and cellular biochemistry · 2026Article
- Targeting IGF2BP3 in Cancer: From Molecular Structure and Biology to Early Drug Discovery.International journal of molecular sciences · 2026Review
- Functional Heterogeneity of Canine Osteosarcoma Cell Lines and Differential Expression ofCells · 2026Article
Corrections and comments
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectiveOsteosarcoma (OS) is a highly aggressive malignant bone tumor. While ID1 plays a critical role in OS progression, the underlying mechanisms remain unclear. This study investigates the METTL3-IGF2BP3 axis-mediated N6-methyladenosine (m
methodsRNA-binding proteins (RBPs) associated with ID1 were predicted using the ENCORI database. Differentially expressed RBP genes (RBP-DEGs) were screened via the GSE253548 dataset, and core RBP-DEGs were identified using machine learning algorithms. m
resultsBioinformatics analysis identified METTL3 and IGF2BP3 as core regulators of ID1, with elevated ID1, IGF2BP3, and METTL3 expression observed in OS cells. Mechanistically, IGF2BP3 enhanced ID1 mRNA stability by binding to m
conclusionThe METTL3-IGF2BP3 axis facilitates OS progression by enhancing ID1 mRNA stability and expression, highlighting its potential as a therapeutic target.
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Registered trials
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