Evidence map›Paper›PMID 29038312›Full record

ArticleEMBO molecular medicine2017

Dynamic stroma reorganization drives blood vessel dysmorphia during glioma growth.

Thomas Mathivet, Claire Bouleti, Matthias Van Woensel, Fabio Stanchi, Tina Verschuere, Li-Kun Phng, Joost Dejaegher, Marly Balcer, Ken Matsumoto, Petya B Georgieva and 6 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

44 citing papers in PubMed, 74 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 4 countries.

Thomas MathivetVascular Patterning Lab, Center for Cancer Biology, VIB, Leuven, Belgium thomas.mathivet@inserm.fr holger.gerhardt@kuleuven.vib.be.ORCID 0000-0001-7761-1684
Claire BouletiVascular Patterning Lab, Center for Cancer Biology, VIB, Leuven, Belgium.
Matthias Van WoenselDepartment of Neurosciences, Laboratory of Experimental Neurosurgery and Neuroanatomy, KU Leuven, Leuven, Belgium.
Fabio StanchiVascular Patterning Lab, Center for Cancer Biology, VIB, Leuven, Belgium.
Tina VerschuereDepartment of Neurosciences, Laboratory of Experimental Neurosurgery and Neuroanatomy, KU Leuven, Leuven, Belgium.
Li-Kun PhngVascular Patterning Lab, Center for Cancer Biology, VIB, Leuven, Belgium.
Joost DejaegherDepartment of Neurosciences, Laboratory of Experimental Neurosurgery and Neuroanatomy, KU Leuven, Leuven, Belgium.
Marly BalcerVascular Patterning Lab, Center for Cancer Biology, VIB, Leuven, Belgium.
Ken MatsumotoVascular Patterning Lab, Center for Cancer Biology, VIB, Leuven, Belgium.
Petya B GeorgievaVascular Patterning Lab, Center for Cancer Biology, VIB, Leuven, Belgium.
Jochen BelmansDepartment of Neurosciences, Laboratory of Experimental Neurosurgery and Neuroanatomy, KU Leuven, Leuven, Belgium.
Raf SciotDepartment of Pathology, KU Leuven and University Hospitals Leuven, Leuven, Belgium.
Christian StockmannUMR 970, Paris Cardiovascular Research Center, Institut National de la Santé et de la Recherche Médicale (INSERM), Paris, France.
Massimiliano MazzoneLab of Molecular Oncology and Angiogenesis, Department of Oncology, KU Leuven, Leuven, Belgium.ORCID 0000-0001-8824-4015
Steven De VleeschouwerDepartment of Neurosciences, Laboratory of Experimental Neurosurgery and Neuroanatomy, KU Leuven, Leuven, Belgium.
Holger GerhardtVascular Patterning Lab, Center for Cancer Biology, VIB, Leuven, Belgium thomas.mathivet@inserm.fr holger.gerhardt@kuleuven.vib.be.ORCID 0000-0002-3030-0384
VIB-KU Leuven Center for Cancer Biology · BEKU Leuven · BEInserm · FRMax Delbrück Center · DE

Funding

European Research Council 311719
6 · The paper itself

Abstract

Glioma growth and progression are characterized by abundant development of blood vessels that are highly aberrant and poorly functional, with detrimental consequences for drug delivery efficacy. The mechanisms driving this vessel dysmorphia during tumor progression are poorly understood. Using longitudinal intravital imaging in a mouse glioma model, we identify that dynamic sprouting and functional morphogenesis of a highly branched vessel network characterize the initial tumor growth, dramatically changing to vessel expansion, leakage, and loss of branching complexity in the later stages. This vascular phenotype transition was accompanied by recruitment of predominantly pro-inflammatory M1-like macrophages in the early stages, followed by

Indexed as

AnimalsAntibodies, MonoclonalAntineoplastic Agents, AlkylatingBlood VesselsBrain NeoplasmsCell Line, TumorDacarbazineDisease Models, AnimalFemaleGliomaHumansMacrophage Colony-Stimulating FactorMacrophagesMaleMiceMice, Inbred C57BLAntibodies, MonoclonalAntineoplastic Agents, AlkylatingDacarbazineMacrophage Colony-Stimulating FactorProto-Oncogene Proteins c-sisTemozolomideVascular Endothelial Growth Factor Agliomalive imagingmyeloid cellsVEGFvessel dysmorphia

Identifiers

PMID29038312
PMCPMC5709745
OpenAlexW2766272075

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.