Evidence map›Paper›PMID 42170292›Full record

ReviewTranslational lung cancer research2026

Understanding the dual role of granulocyte-macrophage colony-stimulating factor in the lung cancer tumor microenvironment and its therapeutic implications.

Gang Wei, Xuanji Zhu, Rui Zhong

Abstract readReview
In one paragraph

Review in Translational lung cancer research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Gang WeiThe Second Department of Breast Surgery, Jilin Cancer Hospital, Changchun, China.
Xuanji ZhuDepartment of Medical Records Room, The First Hospital of Jilin University, Changchun, China.
Rui ZhongJilin Provincial Key Laboratory of Molecular Diagnostics for Malignant Tumor, Jilin Cancer Hospital, Changchun, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Granulocyte-macrophage colony-stimulating factor (GM-CSF) is a pleiotropic cytokine that plays a complex and critical dual regulatory role in the development, progression, and immunotherapy of lung cancer. In recent years, with the deepening of research into the tumor microenvironment (TME), GM-CSF has been recognized to possess dual regulatory functions. On the one hand, GM-CSF can enhance anti-tumor immune responses by activating and recruiting immune cells. On the other hand, it may indirectly support tumor growth and immune evasion by promoting the accumulation of myeloid-derived suppressor cells (MDSCs) and tumor-associated inflammation. Consequently, the precise mechanisms and regulatory networks of GM-CSF within the lung cancer TME remain controversial, and its efficacy in different immunotherapeutic strategies requires further exploration. This review systematically summarizes the biological characteristics of GM-CSF and its expression features in lung cancer, focusing on its dual regulatory effects on immune cells within the TME, including differential modulation of tumor-associated macrophages (TAMs), MDSCs, tumor-associated neutrophils (TANs), and dendritic cells (DCs). Furthermore, this review discusses the potential application value of GM-CSF in lung cancer treatment, such as its combination with chemoradiotherapy, targeted therapy, and immune checkpoint inhibitors (ICIs) based on clinical trial evidence. Finally, we propose key directions for future research, including dissecting GM-CSF's functional determinants using single-cell multi-omics, developing biomarkers for patient stratification, and exploring novel targeted delivery systems. This review aims to provide new insights and directions for future clinical translational research and precision therapy applications of GM-CSF in lung cancer.

Indexed as

dual regulationGranulocyte-macrophage colony-stimulating factor (GM-CSF)immunotherapylung cancertumor microenvironment (TME)

Identifiers

PMID42170292
PMCPMC13186654

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.