Evidence map›Paper›PMID 40297580›Full record

ReviewFrontiers in immunology2025

Immunocytes in the tumor microenvironment: recent updates and interconnections.

Jiyao Yu, Li Fu, Rui Wu, Linyi Che, Guodong Liu, Qinwen Ran, Zhiwei Xia, Xisong Liang, Guanjian Zhao

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 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing 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

42 citing papers in PubMed.

  1. Review
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  6. Metabolomic, in vitro and preclinical evaluation of Auricularia polytricha mushroom.International microbiology : the official journal of the Spanish Society for Microbiology · 2026
    Article
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  8. Review
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  10. Article
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  15. Targeting the COX-2/PGECancer immunology, immunotherapy : CII · 2026
    Review
  16. Article
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  20. 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

9 authors.

Jiyao Yu *Department of Ultrasound, The Second Affiliated Hospital, Chongqing Medical University, Chongqing, China.
Li Fu *Department of Neurosurgery, The Second Affiliated Hospital, Chongqing Medical University, Chongqing, China.
Rui Wu *Department of Neurosurgery, The Second Affiliated Hospital, Chongqing Medical University, Chongqing, China.
Linyi Che *Department of Neurosurgery, The Second Affiliated Hospital, Chongqing Medical University, Chongqing, China.
Guodong LiuDepartment of Neurosurgery, The Second Affiliated Hospital, Chongqing Medical University, Chongqing, China.
Qinwen RanGeneral Practice Department, Wufu Town Hospital, Chongqing, China.
Zhiwei XiaDepartment of Neurology, Hunan Aerospace Hospital, Hunan Normal University, Changsha, China.
Xisong LiangDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha, China.
Guanjian ZhaoDepartment of Neurosurgery, The Second Affiliated Hospital, Chongqing Medical University, Chongqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tumor microenvironment (TME) is a complex, dynamic ecosystem where tumor cells interact with diverse immune and stromal cell types. This review provides an overview of the TME's evolving composition, emphasizing its transition from an early pro-inflammatory, immune-promoting state to a later immunosuppressive milieu characterized by metabolic reprogramming and hypoxia. It highlights the dual roles of key immunocytes-including T lymphocytes, natural killer cells, macrophages, dendritic cells, and myeloid-derived suppressor cells-which can either inhibit or support tumor progression based on their phenotypic polarization and local metabolic conditions. The article further elucidates mechanisms of immune cell plasticity, such as the M1/M2 macrophage switch and the balance between effector T cells and regulatory T cells, underscoring their impact on tumor growth and metastasis. Additionally, emerging therapeutic strategies, including checkpoint inhibitors and chimeric antigen receptor (CAR) T and NK cell therapies, as well as approaches targeting metabolic pathways, are discussed as promising avenues to reinvigorate antitumor immunity. By integrating recent molecular insights and clinical advancements, the review underscores the importance of deciphering the interplay between immunocytes and the TME to develop more effective cancer immunotherapies.

Indexed as

NeoplasmsTumor MicroenvironmentAnimalsDendritic CellsHumansImmunotherapyKiller Cells, NaturalMacrophagesMyeloid-Derived Suppressor Cellscancer immunityimmune checkpointsimmunosuppressionlymphocytesmyeloid cells

Identifiers

PMID40297580
PMCPMC12034658

What OpenQuestion holds

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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 OpenQuestion graph.