Evidence map›Paper›PMID 30712288›Full record

ArticleJournal of cellular and molecular medicine2019

Paracellular and transcellular migration of metastatic cells through the cerebral endothelium.

Hildegard Herman, Csilla Fazakas, János Haskó, Kinga Molnár, Ádám Mészáros, Ádám Nyúl-Tóth, Gábor Szabó, Ferenc Erdélyi, Aurel Ardelean, Anca Hermenean and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. Emerging Roles of Cytoneme-Mediated Signaling in Cancer.International journal of molecular sciences · 2026
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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

12 authors at 4 institutions in 2 countries.

Hildegard HermanInstitute of Life Sciences, Vasile Goldiş Western University of Arad, Arad, Romania.
Csilla FazakasInstitute of Biophysics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
János HaskóInstitute of Biophysics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
Kinga MolnárInstitute of Biophysics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
Ádám MészárosInstitute of Biophysics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
Ádám Nyúl-TóthInstitute of Biophysics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
Gábor SzabóMedical Gene Technology Unit, Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, Hungary.
Ferenc ErdélyiMedical Gene Technology Unit, Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, Hungary.
Aurel ArdeleanInstitute of Life Sciences, Vasile Goldiş Western University of Arad, Arad, Romania.
Anca HermeneanInstitute of Life Sciences, Vasile Goldiş Western University of Arad, Arad, Romania.
István A KrizbaiInstitute of Life Sciences, Vasile Goldiş Western University of Arad, Arad, Romania.
Imola WilhelmInstitute of Life Sciences, Vasile Goldiş Western University of Arad, Arad, Romania.ORCID 0000-0003-2366-7337
HUN-REN Szegedi Biológiai Kutatóközpont · HUUniversity of Szeged · HUVasile Goldis Western University of Arad · ROHUN-REN Institute of Experimental Medicine · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer and melanoma are among the most frequent cancer types leading to brain metastases. Despite the unquestionable clinical significance, important aspects of the development of secondary tumours of the central nervous system are largely uncharacterized, including extravasation of metastatic cells through the blood-brain barrier. By using transmission electron microscopy, here we followed interactions of cancer cells and brain endothelial cells during the adhesion, intercalation/incorporation and transendothelial migration steps. We observed that brain endothelial cells were actively involved in the initial phases of the extravasation by extending filopodia-like membrane protrusions towards the tumour cells. Melanoma cells tended to intercalate between endothelial cells and to transmigrate by utilizing the paracellular route. On the other hand, breast cancer cells were frequently incorporated into the endothelium and were able to migrate through the transcellular way from the apical to the basolateral side of brain endothelial cells. When co-culturing melanoma cells with cerebral endothelial cells, we observed N-cadherin enrichment at melanoma-melanoma and melanoma-endothelial cell borders. However, for breast cancer cells N-cadherin proved to be dispensable for the transendothelial migration both in vitro and in vivo. Our results indicate that breast cancer cells are more effective in the transcellular type of migration than melanoma cells.

Indexed as

AnimalsBrain NeoplasmsBreast NeoplasmsCadherinsCell Line, TumorCell MovementCell ProliferationCerebral CortexCoculture TechniquesEndothelial CellsEndothelium, VascularFemaleGene ExpressionHumansMelanocytesMelanoma, ExperimentalCadherinsblood-brain barrierbrain metastasisbreast cancercerebral endothelial cellincorporationintercalationmelanomaN-cadherinparacellulartranscellular

Identifiers

PMID30712288
PMCPMC6433661
OpenAlexW2913325570

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.