Evidence map›Paper›PMID 41459539›Full record

ReviewFrontiers in immunology2025

Tumor associated macrophages in gastric cancer dual roles in immune evasion and clinical implications for targeted therapy.

Chang Wang, Xu Fan, Xiaomen Sun, Yi Xu, Yanna Sun, Jidong Liu

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 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Review
  3. Therapeutic potential of targeting macrophage polarization in metastatic gastric cancer: a review on core mechanisms and clinical progress.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  4. Article
  5. Article
  6. Review
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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

6 authors.

Chang WangCollege of Continuing Education, Liaoning University of Traditional Chinese Medicine, Shenyang, Liaoning, China.
Xu FanCollege of Acupuncture and Tuina, Liaoning University of Traditional Chinese Medicine, Shenyang, Liaoning, China.
Xiaomen SunCollege of Continuing Education, Liaoning University of Traditional Chinese Medicine, Shenyang, Liaoning, China.
Yi XuCollege of Continuing Education, Liaoning University of Traditional Chinese Medicine, Shenyang, Liaoning, China.
Yanna SunCollege of Continuing Education, Liaoning University of Traditional Chinese Medicine, Shenyang, Liaoning, China.
Jidong LiuCollege of Acupuncture and Tuina, Liaoning University of Traditional Chinese Medicine, Shenyang, Liaoning, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastric cancer (GC) remains a major global health burden with persistently high mortality despite therapeutic advances. Accumulating evidence highlights the pivotal role of tumor-associated macrophages (TAMs) in orchestrating gastric tumor progression through immune suppression, angiogenesis, extracellular matrix remodeling, and metastasis. Within the tumor microenvironment (TME), TAMs exhibit functional plasticity, often polarizing toward an M2-like phenotype that promotes immunosuppression and tumorigenicity. These cells actively participate in immune evasion via immune checkpoint expression and cytokine-mediated T cell inhibition, while also facilitating lymphovascular invasion and chemoresistance through exosome-mediated crosstalk. The density and phenotype of TAMs have been associated with prognosis and therapeutic response in GC. Recent studies have proposed TAMs as promising targets for therapy, with strategies focusing on depleting M2 subsets, reprogramming toward M1 phenotypes, and blocking TAM-driven oncogenic signaling. Targeted interventions, including MENK, paclitaxel, and NF-κB inhibitors, have shown potential in preclinical models. This review comprehensively discusses the mechanistic roles of TAMs in GC and evaluates emerging TAM-targeted therapeutic strategies that may enhance the efficacy of immunotherapy and improve patient outcomes.

Indexed as

Immune EvasionStomach NeoplasmsTumor-Associated MacrophagesTumor EscapeAnimalsHumansImmunotherapyMolecular Targeted TherapySignal TransductionTumor Microenvironmentgastric cancerimmune evasionimmunotherapiesprognosistumor-associated macrophagestumor microenvironment

Identifiers

PMID41459539
PMCPMC12738370

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.