Evidence map›Paper›PMID 41112252›Full record

ReviewFrontiers in immunology2025

m6A RNA modification in tumor-associated macrophages: emerging roles in cancer immunity.

Xi Chen, Shanrui Pu, Kun Lian, Lihua Li, Xiulin Jiang

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Ubiquitination and NOncology letters · 2026
    Review
  2. Article
  3. FTO-modulated mJournal of translational medicine · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. CD63Frontiers in cellular and infection microbiology · 2026
    Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Xi Chen *NHC Key Laboratory of Drug Addiction Medicine, Kunming Medical University, Kunming, China.
Shanrui Pu *School of Biosciences, University of Birmingham, Birmingham, United Kingdom.
Kun LianNHC Key Laboratory of Drug Addiction Medicine, Kunming Medical University, Kunming, China.
Lihua LiNHC Key Laboratory of Drug Addiction Medicine, Kunming Medical University, Kunming, China.
Xiulin JiangDepartment of Systems Biology, City of Hope Comprehensive Cancer Center Biomedical Research Center, Monrovia, CA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

N6-methyladenosine (m6A) is the most prevalent internal modification of eukaryotic mRNA and has emerged as a pivotal regulator of gene expression at the post-transcriptional level. In the tumor immune microenvironment, tumor-associated macrophages (TAMs) represent a highly plastic and heterogeneous population that profoundly influences cancer progression, immune evasion, and therapeutic response. Recent studies have uncovered that m6A modification, mediated by dynamic "writers," "erasers," and "readers," exerts critical regulatory effects on TAM differentiation, polarization, and functional reprogramming. By modulating the stability, translation, and decay of transcripts involved in inflammatory signaling, metabolic adaptation, and immune checkpoints, m6A shapes the balance between tumor-promoting (M2-like) and tumor-suppressive (M1-like) macrophage phenotypes. Moreover, dysregulation of m6A machinery in TAMs has been linked to the suppression of anti-tumor immunity and resistance to immunotherapy, highlighting its translational potential as a therapeutic target. This review summarizes current advances in understanding the roles and mechanisms of m6A modification in TAM biology, discusses its implications in tumor immunity, and outlines the challenges and opportunities of targeting the m6A-TAM axis for cancer treatment.

Indexed as

AdenosineNeoplasmsRNA Processing, Post-TranscriptionalTumor-Associated MacrophagesAnimalsGene Expression Regulation, NeoplasticHumansRNA MethylationTumor MicroenvironmentAdenosineN-methyladenosinecancer immunotherapym6A RNA modificationtumor-associated macrophagestumor microenvironmentYTHDF2

Identifiers

PMID41112252
PMCPMC12528062

What OpenQuestion holds

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Registered trials

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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.