Evidence map›Paper›PMID 24311639›Full record

ArticleNeuro-oncology2014

Functional role of endothelial adhesion molecules in the early stages of brain metastasis.

Manuel Sarmiento Soto, Sébastien Serres, Daniel C Anthony, Nicola R Sibson

Open access · bronzeAbstract read
In one paragraph

Article in Neuro-oncology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed
3.2field-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

88 citing papers in PubMed, 122 citations in OpenAlex.

  1. Tumor-Associated Macrophages Promote Brain Metastasis.bioRxiv : the preprint server for biology · 2026
    Article
  2. Article
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  7. EJNMMI radiopharmacy and chemistry · 2025
    Review
  8. Tumor Microenvironment in Melanoma Brain Metastasis: A New Potential Target?International journal of molecular sciences · 2025
    Review
  9. Article
  10. Review
  11. Review
  12. Article
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  14. Article
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  16. Article
  17. Review
  18. Targeting of endothelial cells in brain tumours.Clinical and translational medicine · 2023
    Review
  19. Article
  20. The origin of brain malignancies at the blood-brain barrier.Cellular and molecular life sciences : CMLS · 2023
    Review

28 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

4 authors at 1 institution in 1 country.

Manuel Sarmiento SotoCR-UK/MRC Gray Institute for Radiation Oncology and Biology, Department of Oncology, University of Oxford, Churchill Hospital, Oxford, UK (M.S.S., S. S., N.R.S.; Department of Pharmacology, University of Oxford, Oxford UK (D.C.A.).
Sébastien Serres
Daniel C Anthony
Nicola R Sibson
University of Oxford · GB

Funding

Cancer Research UK 16945Cancer Research UK C5255/A12678
6 · The paper itself

Abstract

backgroundCellular adhesion molecules (CAMs), which are normally associated with leukocyte trafficking, have also been shown to play an essential role in tumor metastasis to non-CNS sites. However, the role played by CAMs in brain metastasis is largely unexplored. It is known that leukocyte recruitment to the brain is very atypical and that mechanisms of disease in peripheral tissues cannot be extrapolated to the brain. Here, we have established the spatiotemporal expression of 12 key CAMs in the initial phases of tumor seeding in 2 different models of brain metastasis.

methodsBALB/c or SCID mice were injected intracardially (10(5) cells/100 μL phosphate-buffered saline with either 4T1-GFP or MDA231BR-GFP cells, respectively (n = 4-6/group), and expression of the CAMs was determined by immunohistochemistry and immunofluorescence colocalisation.

resultsEndothelial expression of E-selectin, VCAM-1, ALCAM, ICAM-1, VLA-4, and β4 integrin was markedly increased early in tumor seeding. At the same time, the natural ligands to these adhesion molecules were highly expressed on the metastatic tumor cells both in vitro and in vivo. Two of these ligands showed particularly high tumor cell expression (ALCAM and VLA-4), and consequently their functional role in tumor seeding was determined. Antibody neutralization of either ALCAM or VLA-4 significantly reduced tumor seeding within the brain (>60% decrease in tumor number/mm(2) brain; P < .05-0.01).

conclusionsThese findings suggest that ALCAM/ALCAM and VLA-4/VCAM-1 interactions play an important functional role in the early stages of metastasis seeding in the brain. Moreover, this work identifies a specific subset of ligand-receptor interactions that may yield new therapeutic and diagnostic targets for brain metastasis.

Indexed as

AnimalsAntibodies, NeutralizingApoptosisBlotting, WesternBrain NeoplasmsBreast NeoplasmsCell Adhesion MoleculesCell MovementCell ProliferationEndothelium, VascularFemaleFluorescent Antibody TechniqueHumansImmunoenzyme TechniquesIntegrin alpha4beta1MiceAntibodies, NeutralizingCell Adhesion MoleculesIntegrin alpha4beta1braincellular adhesion moleculesendotheliummetastasismouseneutralizing antibody

Identifiers

PMID24311639
PMCPMC3956349
OpenAlexW2128956141

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.