Evidence map›Paper›PMID 27515216›Full record

ArticleMedical hypotheses2016

Melanoma exosome induction of endothelial cell GM-CSF in pre-metastatic lymph nodes may result in different M1 and M2 macrophage mediated angiogenic processes.

Joshua L Hood

Abstract read
In one paragraph

Article in Medical hypotheses, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

32 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Review
  3. Integrins as Key Mediators of Metastasis.International journal of molecular sciences · 2025
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Head and neck tumor cells treated with hypofractionated irradiation die via apoptosis and are better taken up by M1-like macrophages.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2022
    Article
  13. Article
  14. Review
  15. Exosomes and organ-specific metastasis.Molecular therapy. Methods & clinical development · 2021
    Review
  16. Review
  17. Exosomes: Emerging Diagnostic and Therapeutic Targets in Cutaneous Diseases.International journal of molecular sciences · 2020
    Review
  18. Exosomes: A Potential Therapeutic Tool Targeting Communications between Tumor Cells and Macrophages.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Review
  19. Review
  20. 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

1 author at 1 institution in 1 country.

Joshua L HoodUniversity of Louisville, Department of Pharmacology and Toxicology and The James Graham Brown Cancer Center, Clinical and Translational Research Building, 505 South Hancock Street, Louisville, KY 40202, United States. Electronic address: joshua.hood@louisville.edu.
University of Louisville · US

Funding

Continuous separation of melanoma exosomes using field-flow fractionationR21GM107894 · NIGMS · UNIVERSITY OF UTAH · PI GALE, BRUCE, HOOD, JOSHUA L. · 2013 to 2015
$575k
NIGMS NIH HHS R21 GM107894
6 · The paper itself

Abstract

Angiogenesis is a key process in the preparation of lymph nodes for melanoma metastasis. Granulocyte macrophage colony stimulating factor (GM-CSF) induces hypoxia inducible factor 1 alpha (HIF-1α) in M1 or HIF-2α in M2 polarized macrophages. HIF-1α promotes neoangiogenesis while HIF-2α facilitates morphogenic normalization of neovasculature. Melanoma exosomes induce GM-CSF expression by endothelial cells in vitro and HIF-1α expression in pre-metastatic lymph nodes in vivo. This suggest a relationship between melanoma exosome induced endothelial GM-CSF and macrophage mediated angiogenesis in lymph nodes. Theoretically, induction of endothelial cell derived GM-CSF by melanoma exosomes mediates different angiogenic functions in pre-metastatic lymph nodes depending on subcapsular sinus (SCS) macrophage polarity. To explore this hypothesis, experiments utilizing melanoma exosomes in a lymph node model are outlined. Despite their opposing immune functions, indirect melanoma exosome stimulation of M1 or M2 SCS macrophages via endothelial derived GM-CSF in lymph nodes may induce different although complementary pro-tumor angiogenic processes.

Indexed as

AnimalsAntigens, NeoplasmBasic Helix-Loop-Helix ProteinsCytokinesEndothelial CellsEndothelial PAS Domain-Containing Protein 1ExosomesGranulocyte-Macrophage Colony-Stimulating FactorHumansHypoxia-Inducible Factor 1, alpha SubunitImmune SystemInterleukin-10Lymphatic MetastasisLymph NodesMacrophagesMelanomaAntigens, NeoplasmBasic Helix-Loop-Helix ProteinsCytokinesEndothelial PAS Domain-Containing Protein 1Granulocyte-Macrophage Colony-Stimulating FactorHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitInterleukin-10Sialic Acid Binding Ig-like Lectin 1

Identifiers

PMID27515216
PMCPMC4988397
OpenAlexW2480563847

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.