Evidence map›Paper›PMID 40007537›Full record

ReviewFrontiers in immunology2025

Insights into CSF-1/CSF-1R signaling: the role of macrophage in radiotherapy.

Qingchao Shang, Pei Zhang, Xiao Lei, Lehui Du, Baolin Qu

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 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Modulation of HMGB1, PRF1, TRAIL, and M-CSF after TARGIT-IORT in breast-conserving surgery: defining a unique acute immune landscape.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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

5 authors.

Qingchao ShangDepartment of Radiation Oncology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Pei ZhangDepartment of Radiation Oncology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Xiao LeiDepartment of Radiation Oncology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Lehui DuDepartment of Radiation Oncology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Baolin QuDepartment of Radiation Oncology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophage plays an important role in homeostasis and immunity, and dysfunctional macrophage polarization is believed to be associated with the pathogenesis of tissue fibrosis and tumor progression. Colony stimulating factor-1 (CSF-1), a polypeptide chain cytokine, through its receptor (CSF-1R) regulates the differentiation of macrophages. Recently, the promising therapeutic potential of CSF-1/CSF-1R signaling pathway inhibition in cancer treatment is widely used. Furthermore, inhibition of CSF-1/CSF-1R signaling combined with radiotherapy has been extensively studied to reduce immunosuppression and promote abscopal effect. In addition, cumulative evidence demonstrated that M2 phenotype macrophage is dominant in tissue fibrosis and the inhibition of CSF-1/CSF-1R signaling pathway ameliorated pulmonary fibrosis, including radiation-induced lung fibrosis. Herein, we provide a comprehensive review of the CSF-1/CSF-1R signaling pathway in radiotherapy, with a focus on advances in macrophage-targeted strategies in the treatment of cancer and pulmonary fibrosis.

Indexed as

Macrophage Colony-Stimulating FactorMacrophagesNeoplasmsReceptor, Macrophage Colony-Stimulating FactorSignal TransductionAnimalsHumansPulmonary FibrosisRadiotherapyCSF1 protein, humanCSF1R protein, humanMacrophage Colony-Stimulating FactorReceptor, Macrophage Colony-Stimulating FactorCSF-1macrophageradiation-induced pulmonary fibrosis (RIPF)radiotherapytumor associate macrophages (TAM)

Identifiers

PMID40007537
PMCPMC11851012

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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.