Evidence map›Paper›PMID 25691457›Full record

ArticleCancer research2015

Interleukin-5 facilitates lung metastasis by modulating the immune microenvironment.

Rinat Zaynagetdinov, Taylor P Sherrill, Linda A Gleaves, Allyson G McLoed, Jamie A Saxon, Arun C Habermann, Linda Connelly, Daniel Dulek, R Stokes Peebles, Barbara Fingleton and 3 more

Abstract read
In one paragraph

Article in Cancer research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed, 2 pooled it
2.7field-weighted citation impact, top 8% of its field
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

87 citing papers in PubMed, 2 syntheses or guidelines pooled it, 128 citations in OpenAlex.

  1. Pooled it
  2. Eosinophils and eosinophil-associated diseases: An update.The Journal of allergy and clinical immunology · 2018
    Pooled it
  3. Article
  4. Progress in Designing Cytokine Antagonist Antibodies for Cancer Therapy.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review
  5. Article
  6. Eosinophils in solid cancers: sentinels, predictors, and therapeutic allies.Journal of experimental & clinical cancer research : CR · 2026
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Targeting Myeloid Cells for Cancer Immunotherapy.Cancer immunology research · 2025
    Review
  16. Article
  17. Review
  18. Review
  19. Review
  20. Harnessing myeloid cells in cancer.Molecular cancer · 2025
    Review

27 more citing papers are in PubMed but not listed here.

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

13 authors at 3 institutions in 3 countries.

Rinat Zaynagetdinov *Department of Medicine, Division of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University, Nashville, TN, USA, 37232.
Taylor P Sherrill *Department of Medicine, Division of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University, Nashville, TN, USA, 37232.
Linda A GleavesDepartment of Medicine, Division of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University, Nashville, TN, USA, 37232.
Allyson G McLoedDepartment of Cancer Biology, Vanderbilt University, Nashville, TN, USA, 37232.
Jamie A SaxonDepartment of Cancer Biology, Vanderbilt University, Nashville, TN, USA, 37232.
Arun C HabermannDepartment of Medicine, Division of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University, Nashville, TN, USA, 37232.
Linda ConnellyDepartment of Pharmaceutical Sciences, University of Hawaii, Hilo, Hawaii, USA, 96720.
Daniel DulekDepartment of Pediatrics, Vanderbilt University, Nashville, TN, USA, 37232.
R Stokes PeeblesDepartment of Medicine, Division of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University, Nashville, TN, USA, 37232.
Barbara FingletonDepartment of Cancer Biology, Vanderbilt University, Nashville, TN, USA, 37232.
Fiona E YullDepartment of Cancer Biology, Vanderbilt University, Nashville, TN, USA, 37232.
Georgios T StathopoulosLaboratory for Molecular Respiratory Carcinogenesis, Department of Physiology, University of Patras, 26504 Rio, Greece.
Timothy S BlackwellDepartment of Medicine, Division of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University, Nashville, TN, USA, 37232.
Vanderbilt University · USUniversity of Hawaii at Hilo · USUniversity of Patras · GR

Funding

UH Hilo COP A&RP20GM103466 · NIGMS · UNIVERSITY OF HAWAII AT MANOA · PI Peter R Hoffmann · 2012 to 2026
$60.3M
Interdisciplinary Training Program in Lung ResearchT32HL094296 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Ray Stokes Peebles · 2008 to 2026
$6.3M
NHLBI NIH HHS T32 HL094296NHLBI NIH HHS T32HL094296NIGMS NIH HHS P20 GM103466
6 · The paper itself

Abstract

Although the lung is the most common metastatic site for cancer cells, biologic mechanisms regulating lung metastasis are not fully understood. Using heterotopic and intravenous injection models of lung metastasis in mice, we found that IL5, a cytokine involved in allergic and infectious diseases, facilitates metastatic colonization through recruitment of sentinel eosinophils and regulation of other inflammatory/immune cells in the microenvironment of the distal lung. Genetic IL5 deficiency offered marked protection of the lungs from metastasis of different types of tumor cells, including lung cancer, melanoma, and colon cancer. IL5 neutralization protected subjects from metastasis, whereas IL5 reconstitution or adoptive transfer of eosinophils into IL5-deficient mice exerted prometastatic effects. However, IL5 deficiency did not affect the growth of the primary tumor or the size of metastatic lesions. Mechanistic investigations revealed that eosinophils produce CCL22, which recruits regulatory T cells to the lungs. During early stages of metastasis, Treg created a protumorigenic microenvironment, potentially by suppressing IFNγ-producing natural killer cells and M1-polarized macrophages. Together, our results establish a network of allergic inflammatory circuitry that can be co-opted by metastatic cancer cells to facilitate lung colonization, suggesting interventions to target this pathway may offer therapeutic benefits to prevent or treat lung metastasis.

Indexed as

AnimalsCarcinoma, Lewis LungCell Line, TumorEosinophilsFemaleInterleukin-5LungLung NeoplasmsMaleMiceMice, Inbred C57BLMice, KnockoutT-Lymphocytes, RegulatoryTumor EscapeTumor MicroenvironmentInterleukin-5

Identifiers

PMID25691457
PMCPMC4401663
OpenAlexW2086906563

What OpenQuestion holds

Textmetadata
LicenceTDM
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.