Evidence map›Paper›PMID 25692137›Full record

ArticleBioMed research international2015

Melanoma cells homing to the brain: an in vitro model.

A Rizzo, C Vasco, V Girgenti, V Fugnanesi, C Calatozzolo, A Canazza, A Salmaggi, L Rivoltini, M Morbin, E Ciusani

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Melanoma Brain Metastasis: Mechanisms, Models, and Medicine.International journal of molecular sciences · 2016
    Review
  11. Article
  12. 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

10 authors at 4 institutions in 1 country.

A RizzoLaboratory of Clinical Pathology and Medical Genetics, Foundation IRCCS Neurological Institute Carlo Besta, Via Celoria 11, 20133 Milano, Italy.
C VascoLaboratory of Clinical Pathology and Medical Genetics, Foundation IRCCS Neurological Institute Carlo Besta, Via Celoria 11, 20133 Milano, Italy.
V GirgentiLaboratory of Clinical Pathology and Medical Genetics, Foundation IRCCS Neurological Institute Carlo Besta, Via Celoria 11, 20133 Milano, Italy.
V FugnanesiU.O. Neuropathology, IRCCS Foundation C. Besta Neurological Institute, Foundation IRCCS Neurological Institute C. Besta, Via Celoria 11, 20133 Milano, Italy.
C CalatozzoloU.O. Neuropathology, IRCCS Foundation C. Besta Neurological Institute, Foundation IRCCS Neurological Institute C. Besta, Via Celoria 11, 20133 Milano, Italy.
A CanazzaCellular Neurobiology Laboratory, Cerebrovascular Diseases Unit, Foundation IRCCS Neurological Institute C. Besta, Via Celoria 11, 20133 Milano, Italy.
A SalmaggiNeurologia-Stroke Unit, Manzoni Hospital, Via dell'Eremo 9/11, 23900 Lecco, Italy.
L RivoltiniUnit of Immunotherapy, Fondazione IRCCS National Cancer Institute, Via Venezian 1, 20133 Milan, Italy.
M MorbinU.O. Neuropathology, IRCCS Foundation C. Besta Neurological Institute, Foundation IRCCS Neurological Institute C. Besta, Via Celoria 11, 20133 Milano, Italy.
E CiusaniLaboratory of Clinical Pathology and Medical Genetics, Foundation IRCCS Neurological Institute Carlo Besta, Via Celoria 11, 20133 Milano, Italy.
Fondazione IRCCS Istituto Neurologico Carlo Besta · ITAlessandro Manzoni Hospital · ITFondazione IRCCS Istituto Nazionale dei Tumori · ITInstitute of Neurological Sciences · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We developed an in vitro contact through-feet blood brain barrier (BBB) model built using type IV collagen, rat astrocytes, and human umbilical vein endothelial cells (HUVECs) cocultured through Transwell porous polycarbonate membrane. The contact between astrocytes and HUVECs was demonstrated by electron microscopy: astrocytes endfeet pass through the 8.0 μm pores inducing HUVECs to assume a cerebral phenotype. Using this model we evaluated transmigration of melanoma cells from two different patients (M1 and M2) selected among seven melanoma primary cultures. M2 cells showed a statistically significant higher capability to pass across the in vitro BBB model, compared to M1. Expression of adhesion molecules was evaluated by flow cytometry: a statistically significant increased expression of MCAM, αvβ3, and CD49b was detected in M1. PCR array data showed that M2 had a higher expression of several matrix metalloproteinase proteins (MMPs) compared to M1. Specifically, data suggest that MMP2 and MMP9 could be directly involved in BBB permeability and that brain invasion by melanoma cells could be related to the overexpression of many MMPs. Future studies will be necessary to deepen the mechanisms of central nervous system invasion.

Indexed as

Models, BiologicalAnimalsBlood-Brain BarrierGene Expression Regulation, NeoplasticHumansHuman Umbilical Vein Endothelial CellsMelanomaNeoplasm InvasivenessNeoplasm ProteinsRatsTumor Cells, CulturedNeoplasm Proteins

Identifiers

PMID25692137
PMCPMC4321090
OpenAlexW2032475552

What OpenQuestion holds

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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.