Evidence map›Paper›PMID 16524486›Full record

ArticleBMC cancer2006

The fibrinolytic system facilitates tumor cell migration across the blood-brain barrier in experimental melanoma brain metastasis.

George Perides, Yuzheng Zhuge, Tina Lin, Monique F Stins, Roderick T Bronson, Julian K Wu

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

18 citing papers in PubMed, 37 citations in OpenAlex.

  1. Profibrinolytic Factors and Cancer Progression, Metastasis, and Survival.Arteriosclerosis, thrombosis, and vascular biology · 2025
    Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
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  8. Foe or friend? Janus-faces of the neurovascular unit in the formation of brain metastases.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2018
    Review
  9. Article
  10. From plasminogen to plasmin: role of plasminogen receptors in human cancer.International journal of molecular sciences · 2014
    Review
  11. Review
  12. Role of the blood-brain barrier in the formation of brain metastases.International journal of molecular sciences · 2013
    Review
  13. Cell surface remodeling by plasmin: a new function for an old enzyme.Journal of biomedicine & biotechnology · 2012
    Review
  14. Review
  15. Article
  16. Article
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  18. 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

6 authors at 4 institutions in 1 country.

George PeridesDepartment of Surgery, Division of Neurosurgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA. gperides@tufts-nemc.org
Yuzheng Zhuge
Tina Lin
Monique F Stins
Roderick T Bronson
Julian K Wu
Harvard University · USDana-Farber/Harvard Cancer Center · USJohns Hopkins University · USTufts Medical Center · US

Funding

In Vitro Model of the Human Blood Brain Barrier to studyR01MH063850 · NIMH · JOHNS HOPKINS UNIVERSITY · PI STINS, MONIQUE F. · 2001 to 2003
$491k
NIMH NIH HHS R01 MH063850
6 · The paper itself

Abstract

backgroundPatients with metastatic tumors to the brain have a very poor prognosis. Increased metastatic potential has been associated with the fibrinolytic system. We investigated the role of the fibrinolytic enzyme plasmin in tumor cell migration across brain endothelial cells and growth of brain metastases in an experimental metastatic melanoma model.

methodsMetastatic tumors to the brain were established by direct injection into the striatum or by intracarotid injection of B16F10 mouse melanoma cells in C57Bl mice. The role of plasminogen in the ability of human melanoma cells to cross a human blood-brain barrier model was studied on a transwell system.

resultsWild type mice treated with the plasmin inhibitor epsilon-aminocaproic acid (EACA) and plg-/- mice developed smaller tumors and survived longer than untreated wild type mice. Tumors metastasized to the brain of wild type mice treated with EACA and plg-/- less efficiently than in untreated wild type mice. No difference was observed in the tumor growth in any of the three groups of mice. Human melanoma cells were able to cross the human blood-brain barrier model in a plasmin dependent manner.

conclusionPlasmin facilitates the development of tumor metastasis to the brain. Inhibition of the fibrinolytic system could be considered as means to prevent tumor metastasis to the brain.

Indexed as

Aminocaproic AcidAnimalsAntifibrinolytic AgentsBlood-Brain BarrierBrainBrain NeoplasmsCarotid ArteriesCell Line, TumorCell MovementCells, CulturedEndothelium, VascularHumansInjectionsMelanoma, ExperimentalMiceMice, Inbred C57BLAminocaproic AcidAntifibrinolytic AgentsPlasminogen

Identifiers

PMID16524486
PMCPMC1421425
OpenAlexW1754389422

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.