Evidence map›Paper›PMID 41200171›Full record

ReviewFrontiers in immunology2025

Innate immunity in tumors: roles and therapeutic targets.

Songze Leng, Yuyue Ren, Yaoyao Tian, Weiwei Zhao, Yue Mou, Xingyu Chen, Hong Zhou, Wei Wang

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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Interleukin-1β Gene (Current oncology (Toronto, Ont.) · 2026
    Article
  3. Article
  4. Article
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

8 authors.

Songze LengDepartment of Hematology, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Yuyue RenDepartment of Hematology, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Yaoyao TianDepartment of Hematology, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Weiwei ZhaoDepartment of Hematology, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Yue MouDepartment of Hematology, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Xingyu ChenDepartment of Hematology, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Hong ZhouDepartment of Hematology, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Wei WangDepartment of Hematology, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Innate immune cells and pathways are central to shaping the tumor microenvironment (TME), where they influence tumor growth, metastasis, and responsiveness to immunotherapy. Although research on innate immunity in cancer has expanded considerably, the mechanisms driving immune dysfunction remain incompletely understood. This review summarizes current knowledge on the functional states of innate immune cells within the TME and highlights how metabolic reprogramming contributes to immune suppression and tumor progression. We further discuss recent advances in therapeutic strategies targeting innate immune pathways, emphasizing their translational potential. Importantly, we also examine unresolved controversies and knowledge gaps across innate immune cells, metabolic networks, and innate immune factors such as complement and cytokines, outlining key challenges for clinical translation. By linking mechanistic insights with emerging interventions and identifying future directions, this review provides a framework for integrating innate immunity into next-generation cancer treatment.

Indexed as

Immunity, InnateNeoplasmsAnimalsCytokinesHumansImmunotherapyTumor MicroenvironmentCytokinesimmune cellsimmune factorsimmunotherapyinnate immunitytumor microenvironment

Identifiers

PMID41200171
PMCPMC12585967

What OpenQuestion 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 OpenQuestion graph.