ReviewFrontiers in immunology2026
Rewriting the RNA code: an m
Review in Frontiers in immunology, 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.
- Decoding the tumor-aging axis: from bench to clinical.Frontiers in immunology · 2026Review
- Non-coding RNAs in cancer: multi-omics insights, liquid biopsy advances, drug resistance mechanisms, and the road to clinical translation.Frontiers in oncology · 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
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: The epitranscriptome, particularly N Methods: We synthesized current evidence through systematic reviews of primary research and high-impact papers from PubMed and Google Scholar, focusing on the mechanistic role of m Results: We classify tumors into Writer-Dominant (METTL3/14-high, Eraser-High (FTO/ALKBH5-high), Reader-Amplified (IGF2BP/YTHDF-high), and Immune-Modulatory subtypes, each with distinct oncogenic programs, therapy resistance mechanisms, and, crucially, actionable therapeutic vulnerabilities. We provide explicit, evidence-based molecular and functional inclusion criteria for each subtype and acknowledge that tumors can exhibit hybrid features, which directly inform rational combination strategies. Furthermore, we detail a diagnostic-therapeutic roadmap that integrates liquid biopsy-based m Conclusion: Targeting the m
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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.