Evidence map›Paper›PMID 27454178›Full record

ArticlePloS one2016

Establishment and Characterization of a Tumor Stem Cell-Based Glioblastoma Invasion Model.

Stine Skov Jensen, Morten Meyer, Stine Asferg Petterson, Bo Halle, Ann Mari Rosager, Charlotte Aaberg-Jessen, Mads Thomassen, Mark Burton, Torben A Kruse, Bjarne Winther Kristensen

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
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  4. Advances in Research of Adult Gliomas.International journal of molecular sciences · 2021
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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

10 authors at 2 institutions in 1 country.

Stine Skov JensenDepartment of Pathology, Odense University Hospital, Denmark, Odense C, Denmark.
Morten MeyerDepartment of Neurobiology Research, Institute of Molecular Medicine, University of Southern Denmark, Odense C, Denmark.
Stine Asferg PettersonDepartment of Pathology, Odense University Hospital, Denmark, Odense C, Denmark.ORCID http://orcid.org/0000-0001-9963-7295
Bo HalleDepartment of Pathology, Odense University Hospital, Denmark, Odense C, Denmark.
Ann Mari RosagerDepartment of Pathology, Odense University Hospital, Denmark, Odense C, Denmark.
Charlotte Aaberg-JessenDepartment of Pathology, Odense University Hospital, Denmark, Odense C, Denmark.
Mads ThomassenDepartment of Clinical Research, University of Southern Denmark, Odense C, Denmark.
Mark BurtonDepartment of Clinical Research, University of Southern Denmark, Odense C, Denmark.
Torben A KruseDepartment of Clinical Research, University of Southern Denmark, Odense C, Denmark.
Bjarne Winther KristensenDepartment of Pathology, Odense University Hospital, Denmark, Odense C, Denmark.
University of Southern Denmark · DKOdense University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsGlioblastoma is the most frequent and malignant brain tumor. Recurrence is inevitable and most likely connected to tumor invasion and presence of therapy resistant stem-like tumor cells. The aim was therefore to establish and characterize a three-dimensional in vivo-like in vitro model taking invasion and tumor stemness into account.

methodsGlioblastoma stem cell-like containing spheroid (GSS) cultures derived from three different patients were established and characterized. The spheroids were implanted in vitro into rat brain slice cultures grown in stem cell medium and in vivo into brains of immuno-compromised mice. Invasion was followed in the slice cultures by confocal time-lapse microscopy. Using immunohistochemistry, we compared tumor cell invasion as well as expression of proliferation and stem cell markers between the models.

resultsWe observed a pronounced invasion into brain slice cultures both by confocal time-lapse microscopy and immunohistochemistry. This invasion closely resembled the invasion in vivo. The Ki-67 proliferation indexes in spheroids implanted into brain slices were lower than in free-floating spheroids. The expression of stem cell markers varied between free-floating spheroids, spheroids implanted into brain slices and tumors in vivo.

conclusionThe established invasion model kept in stem cell medium closely mimics tumor cell invasion into the brain in vivo preserving also to some extent the expression of stem cell markers. The model is feasible and robust and we suggest the model as an in vivo-like model with a great potential in glioma studies and drug discovery.

Indexed as

AnimalsBiomarkersBrain NeoplasmsCell Line, TumorCell MovementCell ProliferationDisease Models, AnimalFemaleGlioblastomaHeterograftsHumansImmunohistochemistryMiceMicroscopy, ConfocalNeoplasm InvasivenessNeoplastic Stem CellsBiomarkers

Identifiers

PMID27454178
PMCPMC4959755
OpenAlexW2476621834

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.