Evidence map›Paper›PMID 41884817›Full record

ReviewFrontiers in immunology2026

Soluble cytokines and chemokines in NSCLC: drivers of immune evasion and angiogenesis.

Liang Yang, Zhijun Fan, Zhe Wang, Dong Zhou

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

4 authors.

Liang Yang *Department of Radiotherapy, Affiliated Zhongshan Hospital of Dalian University, Liaoning, Dalian, China.
Zhijun Fan *Department of Medical Oncology, Affiliated Zhongshan Hospital of Dalian University, Liaoning, Dalian, China.
Zhe WangDepartment of Medical Oncology, Affiliated Zhongshan Hospital of Dalian University, Liaoning, Dalian, China.
Dong ZhouDepartment of Medical Oncology, Affiliated Zhongshan Hospital of Dalian University, Liaoning, Dalian, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-small cell lung cancer (NSCLC) remains a leading cause of cancer-related mortality worldwide. The tumor microenvironment (TME) is characterized by a dynamic network of soluble cytokines and chemokines that orchestrate immune evasion, promote angiogenesis, and facilitate metastatic dissemination. Among these, interleukins such as IL-6, IL-8, and IL-10, along with chemokine axes including CXCL12-CXCR4 and CCL21-CCR7, are critical drivers of tumor progression and resistance to immunotherapy. These mediators modulate immune cell recruitment, epithelial-mesenchymal transition, and vascular remodeling, thereby shaping tumor behavior and therapeutic response. In parallel, angiogenic factors such as VEGF, bFGF, and MMPs promote neovascularization and extracellular matrix degradation, reinforcing metastatic potential. Notably, cytokine signatures in peripheral blood are emerging as prognostic biomarkers and predictive indicators for immune checkpoint blockade efficacy, particularly PD-1 inhibitors. This review systematically summarizes the current understanding of soluble mediator-driven mechanisms in NSCLC progression, including cytokines and chemokines, providing new opportunities for biomarker-guided precision therapy and combination strategies in NSCLC.

Indexed as

Carcinoma, Non-Small-Cell LungChemokinesCytokinesLung NeoplasmsNeovascularization, PathologicTumor EscapeAnimalsHumansTumor MicroenvironmentChemokinesCytokinesangiogenesischemokinecytokineimmunotherapymetastasisnon-small cell lung cancerPD-1soluble mediator

Identifiers

PMID41884817
PMCPMC13011355

What OpenQuestion holds

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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.